Cited by 129Cellular Mechanics and InteractionsProtease and Inhibitor MechanismsTGF-β signaling in diseases

Extracellular matrix dynamics in vascular remodeling

Open access
Ma, Zihan, Mao, Chenfeng, Jia, Yiting, Fu, Yi, Kong, Wei·2020·American Journal of Physiology-Cell Physiology

Abstract

Vascular remodeling is the adaptive response to various physiological and pathophysiological alterations that are closely related to aging and vascular diseases. Understanding the mechanistic regulation of vascular remodeling may be favorable for discovering potential therapeutic targets and strategies. The extracellular matrix (ECM), including matrix proteins and their degradative metalloproteases, serves as the main component of the microenvironment and exhibits dynamic changes during vascular remodeling. This process involves mainly the altered composition of matrix proteins, metalloprotease-mediated degradation, posttranslational modification of ECM proteins, and altered topographical features of the ECM. To date, adequate studies have demonstrated that ECM dynamics also play a critical role in vascular remodeling in various diseases. Here, we review these related studies, summarize how ECM dynamics control vascular remodeling, and further indicate potential diagnostic biomarkers and therapeutic targets in the ECM for corresponding vascular diseases.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1152/ajpcell.00147.2020

Cites

5 of 5 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Vascular density and stability are strongly influenced by ECM composition.

    “Notably, vascular density and stability were strongly influenced by ECM composition 23 .”

    From Vascularized human skin assembloids model compartmental skin organization and immune responsiveness in vitro (2026) · cites this paper as [23]

    The Introduction (page unavailable) reports increased vascular density in TSP-2-knockout mice and says ECM components maintain endothelial integrity. It also links collagen composition to atherosclerotic plaque stability, but does not establish the broader claim that vascular stability is strongly influenced by ECM composition. (LLM, conf=0.84)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 239

  1. [1]Agah A, Kyriakides TR, Lawler J, Bornstein P. The lack of thrombospondin-1 (TSP1) dictates the course of wound healing in double-TSP1/TSP2-null mice. Am J Pathol 161: 831–839, 2002. doi: 10.1016/S0002-9440(10)64243-5. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  2. [2]Aikio M, Alahuhta I, Nurmenniemi S, Suojanen J, Palovuori R, Teppo S, Sorsa T, López-Otín C, Pihlajaniemi T, Salo T, Heljasvaara R, Nyberg P. Arresten, a collagen-derived angiogenesis inhibitor, suppresses invasion of squamous cell carcinoma. PLoS One 7: e51044, 2012. doi: 10.1371/journal.pone.0051044. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  3. [3]Akulapalli S, Boosani CS, Laknaur A, Gunda V. Abstract 4272: Hexastatin is a potent therapeutic agent for targeting tumor angiogenesis and tumor growth. Cancer Res 71: 4272, 2011. doi: 10.1158/1538-7445.AM2011-4272. [DOI] [Google Scholar] · DOI
  4. [4]Ambesi A, McKeown-Longo PJ. Anastellin, the angiostatic fibronectin peptide, is a selective inhibitor of lysophospholipid signaling. Mol Cancer Res 7: 255–265, 2009. doi: 10.1158/1541-7786.MCR-08-0195. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  5. [5]Añazco C, López-Jiménez AJ, Rafi M, Vega-Montoto L, Zhang MZ, Hudson BG, Vanacore RM. Lysyl oxidase-like-2 cross-links collagen iv of glomerular basement membrane. J Biol Chem 291: 25999–26012, 2016. doi: 10.1074/jbc.M116.738856. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  6. [6]Arciniegas E, Neves CY, Candelle D, Parada D. Differential versican isoforms and aggrecan expression in the chicken embryo aorta. Anat Rec A Discov Mol Cell Evol Biol 279A: 592–600, 2004. doi: 10.1002/ar.a.20042. [DOI] [PubMed] [Google Scholar] · DOI
  7. [7]Arikawa-Hirasawa E, Watanabe H, Takami H, Hassell JR, Yamada Y. Perlecan is essential for cartilage and cephalic development. Nat Genet 23: 354–358, 1999. doi: 10.1038/15537. [DOI] [PubMed] [Google Scholar] · DOI
  8. [8]Arikawa-Hirasawa E, Wilcox WR, Le AH, Silverman N, Govindraj P, Hassell JR, Yamada Y. Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene. Nat Genet 27: 431–434, 2001. doi: 10.1038/86941. [DOI] [PubMed] [Google Scholar] · DOI
  9. [9]Avery NC, Bailey AJ. The effects of the Maillard reaction on the physical properties and cell interactions of collagen. Pathol Biol (Paris) 54: 387–395, 2006. doi: 10.1016/j.patbio.2006.07.005. [DOI] [PubMed] [Google Scholar] · DOI
  10. [10]Bagnato C, Thumar J, Mayya V, Hwang SI, Zebroski H, Claffey KP, Haudenschild C, Eng JK, Lundgren DH, Han DK. Proteomics analysis of human coronary atherosclerotic plaque: a feasibility study of direct tissue proteomics by liquid chromatography and tandem mass spectrometry. Mol Cell Proteomics 6: 1088–1102, 2007. doi: 10.1074/mcp.M600259-MCP200. [DOI] [PubMed] [Google Scholar] · DOI
  11. [11]Barascuk N, Genovese F, Larsen L, Byrjalsen I, Zheng Q, Sun S, Hosbond S, Poulsen TS, Diederichsen A, Jensen JM, Mickley H, Register TC, Rasmussen LM, Leeming DJ, Christiansen C, Karsdal MA. A MMP derived versican neo-epitope is elevated in plasma from patients with atherosclerotic heart disease. Int J Clin Exp Med 6: 174–184, 2013. [PMC free article] [PubMed] [Google Scholar]
  12. [12]Bauer RC, Tohyama J, Cui J, Cheng L, Yang J, Zhang X, Ou K, Paschos GK, Zheng XL, Parmacek MS, Rader DJ, Reilly MP. Knockout of Adamts7, a novel coronary artery disease locus in humans, reduces atherosclerosis in mice. Circulation 131: 1202–1213, 2015. doi: 10.1161/CIRCULATIONAHA.114.012669. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  13. [13]Bax DV, Bernard SE, Lomas A, Morgan A, Humphries J, Shuttleworth CA, Humphries MJ, Kielty CM. Cell adhesion to fibrillin-1 molecules and microfibrils is mediated by alpha 5 beta 1 and alpha v beta 3 integrins. J Biol Chem 278: 34605–34616, 2003. doi: 10.1074/jbc.M303159200. [DOI] [PubMed] [Google Scholar] · DOI
  14. [14]Belo VA, Guimarães DA, Castro MM. Matrix Metalloproteinase 2 as a Potential Mediator of Vascular Smooth Muscle Cell Migration and Chronic Vascular Remodeling in Hypertension. J Vasc Res 52: 221–231, 2015. doi: 10.1159/000441621. [DOI] [PubMed] [Google Scholar] · DOI
  15. [15]Bengtsson E, Hultman K, Dunér P, Asciutto G, Almgren P, Orho-Melander M, Melander O, Nilsson J, Hultgårdh-Nilsson A, Gonçalves I. ADAMTS-7 is associated with a high-risk plaque phenotype in human atherosclerosis. Sci Rep 7: 3753, 2017. doi: 10.1038/s41598-017-03573-4. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  16. [16]Bergmeier W, Piffath CL, Cheng G, Dole VS, Zhang Y, von Andrian UH, Wagner DD. Tumor necrosis factor-alpha-converting enzyme (ADAM17) mediates GPIbalpha shedding from platelets in vitro and in vivo. Circ Res 95: 677–683, 2004. doi: 10.1161/01.RES.0000143899.73453.11. [DOI] [PubMed] [Google Scholar] · DOI
  17. [17]Bignon M, Pichol-Thievend C, Hardouin J, Malbouyres M, Bréchot N, Nasciutti L, Barret A, Teillon J, Guillon E, Etienne E, Caron M, Joubert-Caron R, Monnot C, Ruggiero F, Muller L, Germain S. Lysyl oxidase-like protein-2 regulates sprouting angiogenesis and type IV collagen assembly in the endothelial basement membrane. Blood 118: 3979–3989, 2011. doi: 10.1182/blood-2010-10-313296. [DOI] [PubMed] [Google Scholar] · DOI
  18. [18]Brassart-Pasco S, Sénéchal K, Thevenard J, Ramont L, Devy J, Di Stefano L, Dupont-Deshorgue A, Brézillon S, Feru J, Jazeron JF, Diebold MD, Ricard-Blum S, Maquart FX, Monboisse JC. Tetrastatin, the NC1 domain of the α4(IV) collagen chain: a novel potent anti-tumor matrikine. PLoS One 7: e29587, 2012. doi: 10.1371/journal.pone.0029587. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  19. [19]Breslow JL. Transgenic mouse models of lipoprotein metabolism and atherosclerosis. Proc Natl Acad Sci USA 90: 8314–8318, 1993. doi: 10.1073/pnas.90.18.8314. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  20. [20]Briggs MD, Hoffman SM, King LM, Olsen AS, Mohrenweiser H, Leroy JG, Mortier GR, Rimoin DL, Lachman RS, Gaines ES, Cekleniak JA, Knowlton RG, Cohn DH. Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene. Nat Genet 10: 330–336, 1995. doi: 10.1038/ng0795-330. [DOI] [PubMed] [Google Scholar] · DOI
  21. [21]Briones AM, González JM, Somoza B, Giraldo J, Daly CJ, Vila E, González MC, McGrath JC, Arribas SM. Role of elastin in spontaneously hypertensive rat small mesenteric artery remodelling. J Physiol 552: 185–195, 2003. doi: 10.1113/jphysiol.2003.046904. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  22. [22]Byers PH, Duvic M, Atkinson M, Robinow M, Smith LT, Krane SM, Greally MT, Ludman M, Matalon R, Pauker S, Quanbeck D, Schwarze U. Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in the COL1A1 and COL1A2 genes of type I collagen. Am J Med Genet 72: 94–105, 1997. doi: 10.1002/(SICI)1096-8628(19971003)72:1<94:AID-AJMG20>3.0.CO;2-O. [DOI] [PubMed] [Google Scholar] · DOI
  23. [23]Canault M, Peiretti F, Kopp F, Bonardo B, Bonzi MF, Coudeyre JC, Alessi MC, Juhan-Vague I, Nalbone G. The TNF alpha converting enzyme (TACE/ADAM17) is expressed in the atherosclerotic lesions of apolipoprotein E-deficient mice: possible contribution to elevated plasma levels of soluble TNF alpha receptors. Atherosclerosis 187: 82–91, 2006. doi: 10.1016/j.atherosclerosis.2005.08.031. [DOI] [PubMed] [Google Scholar] · DOI
  24. [24]Chen D, Asahara T, Krasinski K, Witzenbichler B, Yang J, Magner M, Kearney M, Frazier WA, Isner JM, Andrés V. Antibody blockade of thrombospondin accelerates reendothelialization and reduces neointima formation in balloon-injured rat carotid artery. Circulation 100: 849–854, 1999. doi: 10.1161/01.CIR.100.8.849. [DOI] [PubMed] [Google Scholar] · DOI
  25. [25]Chung IM, Gold HK, Schwartz SM, Ikari Y, Reidy MA, Wight TN. Enhanced extracellular matrix accumulation in restenosis of coronary arteries after stent deployment. J Am Coll Cardiol 40: 2072–2081, 2002. doi: 10.1016/S0735-1097(02)02598-6. [DOI] [PubMed] [Google Scholar] · DOI
  26. [26]Cloos PA, Christgau S. Post-translational modifications of proteins: implications for aging, antigen recognition, and autoimmunity. Biogerontology 5: 139–158, 2004. doi: 10.1023/B:BGEN.0000031152.31352.8b. [DOI] [PubMed] [Google Scholar] · DOI
  27. [27]Cocciolone AJ, Hawes JZ, Staiculescu MC, Johnson EO, Murshed M, Wagenseil JE. Elastin, arterial mechanics, and cardiovascular disease. Am J Physiol Heart Circ Physiol 315: H189–H205, 2018. doi: 10.1152/ajpheart.00087.2018. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  28. [28]Coles EG, Gammill LS, Miner JH, Bronner-Fraser M. Abnormalities in neural crest cell migration in laminin alpha5 mutant mice. Dev Biol 289: 218–228, 2006. doi: 10.1016/j.ydbio.2005.10.031. [DOI] [PubMed] [Google Scholar] · DOI
  29. [29]Colige A, Monseur C, Crawley JTB, Santamaria S, de Groot R. Proteomic discovery of substrates of the cardiovascular protease ADAMTS7. J Biol Chem 294: 8037–8045, 2019. doi: 10.1074/jbc.RA119.007492. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  30. [30]Cong L, Jia J. Promoter polymorphisms which regulate ADAM9 transcription are protective against sporadic Alzheimer’s disease. Neurobiol Aging 32: 54–62, 2011. doi: 10.1016/j.neurobiolaging.2009.01.001. [DOI] [PubMed] [Google Scholar] · DOI
  31. [31]Coronary Artery Disease (C4D) Genetics Consortium A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. Nat Genet 43: 339–344, 2011. doi: 10.1038/ng.782. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  32. [32]Cosemans JMEM, Kuijpers MJE, Lecut C, Loubele STBG, Heeneman S, Jandrot-Perrus M, Heemskerk JWM. Contribution of platelet glycoprotein VI to the thrombogenic effect of collagens in fibrous atherosclerotic lesions. Atherosclerosis 181: 19–27, 2005. doi: 10.1016/j.atherosclerosis.2004.12.037. [DOI] [PubMed] [Google Scholar] · DOI
  33. [33]Costell M, Carmona R, Gustafsson E, González-Iriarte M, Fässler R, Muñoz-Chápuli R. Hyperplastic conotruncal endocardial cushions and transposition of great arteries in perlecan-null mice. Circ Res 91: 158–164, 2002. doi: 10.1161/01.RES.0000026056.81424.DA. [DOI] [PubMed] [Google Scholar] · DOI
  34. [34]Costell M, Gustafsson E, Aszódi A, Mörgelin M, Bloch W, Hunziker E, Addicks K, Timpl R, Fässler R. Perlecan maintains the integrity of cartilage and some basement membranes. J Cell Biol 147: 1109–1122, 1999. doi: 10.1083/jcb.147.5.1109. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  35. [35]Dalgleish R. The Human Collagen Mutation Database 1998. Nucleic Acids Res 26: 253–255, 1998. doi: 10.1093/nar/26.1.253. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  36. [36]Damiana T, Damgaard D, Sidelmann JJ, Nielsen CH, de Maat MPM, Münster AB, Palarasah Y. Citrullination of fibrinogen by peptidylarginine deiminase 2 impairs fibrin clot structure. Clin Chim Acta 501: 6–11, 2020. doi: 10.1016/j.cca.2019.10.033. [DOI] [PubMed] [Google Scholar] · DOI
  37. [37]Dasouki M, Markova D, Garola R, Sasaki T, Charbonneau NL, Sakai LY, Chu ML. Compound heterozygous mutations in fibulin-4 causing neonatal lethal pulmonary artery occlusion, aortic aneurysm, arachnodactyly, and mild cutis laxa (Abstract). Am J Med Genet A 143A: 2635–2641, 2007. doi: 10.1002/ajmg.a.31980. [DOI] [PubMed] [Google Scholar] · DOI
  38. [38]Dean RA, Overall CM. Proteomics discovery of metalloproteinase substrates in the cellular context by iTRAQ labeling reveals a diverse MMP-2 substrate degradome. Mol Cell Proteomics 6: 611–623, 2007. doi: 10.1074/mcp.M600341-MCP200. [DOI] [PubMed] [Google Scholar] · DOI
  39. [39]Dhar S, Sun Z, Meininger GA, Hill MA. Nonenzymatic glycation interferes with fibronectin-integrin interactions in vascular smooth muscle cells. Microcirculation 24: e12347, 2017. doi: 10.1111/micc.12347. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  40. [40]Di Russo J, Luik AL, Yousif L, Budny S, Oberleithner H, Hofschröer V, Klingauf J, van Bavel E, Bakker EN, Hellstrand P, Bhattachariya A, Albinsson S, Pincet F, Hallmann R, Sorokin LM. Endothelial basement membrane laminin 511 is essential for shear stress response. EMBO J 36: 183–201, 2017. doi: 10.15252/embj.201694756. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  41. [41]Didangelos A, Yin X, Mandal K, Baumert M, Jahangiri M, Mayr M. Proteomics characterization of extracellular space components in the human aorta. Mol Cell Proteomics 9: 2048–2062, 2010. doi: 10.1074/mcp.M110.001693. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  42. [42]Dietz HC, Cutting GR, Pyeritz RE, Maslen CL, Sakai LY, Corson GM, Puffenberger EG, Hamosh A, Nanthakumar EJ, Curristin SM, Stetten G, Meyers DA, Francomano CA. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene. Nature 352: 337–339, 1991. doi: 10.1038/352337a0. [DOI] [PubMed] [Google Scholar] · DOI
  43. [43]Dixelius J, Cross M, Matsumoto T, Sasaki T, Timpl R, Claesson-Welsh L. Endostatin regulates endothelial cell adhesion and cytoskeletal organization. Cancer Res 62: 1944–1947, 2002. [PubMed] [Google Scholar]
  44. [44]Donners MM, Wolfs IM, Olieslagers S, Mohammadi-Motahhari Z, Tchaikovski V, Heeneman S, van Buul JD, Caolo V, Molin DG, Post MJ, Waltenberger J. A disintegrin and metalloprotease 10 is a novel mediator of vascular endothelial growth factor-induced endothelial cell function in angiogenesis and is associated with atherosclerosis. Arterioscler Thromb Vasc Biol 30: 2188–2195, 2010. doi: 10.1161/ATVBAHA.110.213124. [DOI] [PubMed] [Google Scholar] · DOI
  45. [45]Douglass S, Goyal A, Iozzo RV. The role of perlecan and endorepellin in the control of tumor angiogenesis and endothelial cell autophagy. Connect Tissue Res 56: 381–391, 2015. doi: 10.3109/03008207.2015.1045297. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  46. [46]Du Y, Gao C, Liu Z, Wang L, Liu B, He F, Zhang T, Wang Y, Wang X, Xu M, Luo GZ, Zhu Y, Xu Q, Wang X, Kong W. Upregulation of a disintegrin and metalloproteinase with thrombospondin motifs-7 by miR-29 repression mediates vascular smooth muscle calcification. Arterioscler Thromb Vasc Biol 32: 2580–2588, 2012. doi: 10.1161/ATVBAHA.112.300206. [DOI] [PubMed] [Google Scholar] · DOI
  47. [47]Du Y, Wang Y, Wang L, Liu B, Tian Q, Liu CJ, Zhang T, Xu Q, Zhu Y, Ake O, Qi Y, Tang C, Kong W, Wang X. Cartilage oligomeric matrix protein inhibits vascular smooth muscle calcification by interacting with bone morphogenetic protein-2. Circ Res 108: 917–928, 2011. doi: 10.1161/CIRCRESAHA.110.234328. [DOI] [PubMed] [Google Scholar] · DOI
  48. [48]Dyczynska E, Sun D, Yi H, Sehara-Fujisawa A, Blobel CP, Zolkiewska A. Proteolytic processing of delta-like 1 by ADAM proteases. J Biol Chem 282: 436–444, 2007. doi: 10.1074/jbc.M605451200. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  49. [49]Evanko SP, Angello JC, Wight TN. Formation of hyaluronan- and versican-rich pericellular matrix is required for proliferation and migration of vascular smooth muscle cells. Arterioscler Thromb Vasc Biol 19: 1004–1013, 1999. doi: 10.1161/01.ATV.19.4.1004. [DOI] [PubMed] [Google Scholar] · DOI
  50. [50]Faury G, Pezet M, Knutsen RH, Boyle WA, Heximer SP, McLean SE, Minkes RK, Blumer KJ, Kovacs A, Kelly DP, Li DY, Starcher B, Mecham RP. Developmental adaptation of the mouse cardiovascular system to elastin haploinsufficiency. J Clin Invest 112: 1419–1428, 2003. doi: 10.1172/JCI19028. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  51. [51]Fava M, Barallobre-Barreiro J, Mayr U, Lu R, Didangelos A, Baig F, Lynch M, Catibog N, Joshi A, Barwari T, Yin X, Jahangiri M, Mayr M. Role of ADAMTS-5 in aortic dilatation and extracellular matrix remodeling. Arterioscler Thromb Vasc Biol 38: 1537–1548, 2018. doi: 10.1161/ATVBAHA.117.310562. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  52. [52]Folkman J. Angiogenesis: an organizing principle for drug discovery? Nat Rev Drug Discov 6: 273–286, 2007. doi: 10.1038/nrd2115. [DOI] [PubMed] [Google Scholar] · DOI
  53. [53]Foster MW, Hess DT, Stamler JS. Protein S-nitrosylation in health and disease: a current perspective. Trends Mol Med 15: 391–404, 2009. doi: 10.1016/j.molmed.2009.06.007. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
  54. [54]Freyberg MA, Kaiser D, Graf R, Buttenbender J, Friedl P. Proatherogenic flow conditions initiate endothelial apoptosis via thrombospondin-1 and the integrin-associated protein. Biochem Biophys Res Commun 286: 141–149, 2001. doi: 10.1006/bbrc.2001.5314. [DOI] [PubMed] [Google Scholar] · DOI
  55. [55]Frieda S, Pearce A, Wu J, Silverstein RL. Recombinant GST/CD36 fusion proteins define a thrombospondin binding domain. Evidence for a single calcium-dependent binding site on CD36. J Biol Chem 270: 2981–2986, 1995. doi: 10.1074/jbc.270.7.2981. [DOI] [PubMed] [Google Scholar] · DOI
  56. [56]Frieser M, Nöckel H, Pausch F, Röder C, Hahn A, Deutzmann R, Sorokin LM. Cloning of the mouse laminin alpha 4 cDNA. Expression in a subset of endothelium. Eur J Biochem 246: 727–735, 1997. doi: 10.1111/j.1432-1033.1997.t01-1-00727.x. [DOI] [PubMed] [Google Scholar] · DOI
  57. [57]Fu Y, Gao C, Liang Y, Wang M, Huang Y, Ma W, Li T, Jia Y, Yu F, Zhu W, Cui Q, Li Y, Xu Q, Wang X, Kong W. Shift of Macrophage Phenotype Due to Cartilage Oligomeric Matrix Protein Deficiency Drives Atherosclerotic Calcification. Circ Res 119: 261–276, 2016. doi: 10.1161/CIRCRESAHA.115.308021. [DOI] [PubMed] [Google Scholar] · DOI
  58. [58]Gaggar A, Jackson PL, Noerager BD, O’Reilly PJ, McQuaid DB, Rowe SM, Clancy JP, Blalock JE. A novel proteolytic cascade generates an extracellular matrix-derived chemoattractant in chronic neutrophilic inflammation. J Immunol 180: 5662–5669, 2008. doi: 10.4049/jimmunol.180.8.5662. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  59. [59]Gao Y, Wu W, Yu C, Zhong F, Li G, Kong W, Zheng J. A disintegrin and metalloproteinase with thrombospondin motif 1 (ADAMTS1) expression increases in acute aortic dissection. Sci China Life Sci 59: 59–67, 2016. doi: 10.1007/s11427-015-4959-4. [DOI] [PubMed] [Google Scholar] · DOI
  60. [60]Gao YX, Yu CA, Lu JH, Gao HM, Li G, Kong W, Zheng J. ADAMTS-7 expression increases in the early stage of angiotensin II-induced renal injury in elderly mice. Kidney Blood Press Res 38: 121–131, 2013. doi: 10.1159/000355758. [DOI] [PubMed] [Google Scholar] · DOI
  61. [61]Geraldino-Pardilla L, Giles JT, Sokolove J, Zartoshti A, Robinson WH, Budoff M, Detrano R, Bokhari S, Bathon JM. Association of anti-citrullinated peptide antibodies with coronary artery calcification in rheumatoid arthritis. Arthritis Care Res (Hoboken) 69: 1276–1281, 2017. doi: 10.1002/acr.23106. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  62. [62]Getachew R, Ballinger ML, Burch ML, Reid JJ, Khachigian LM, Wight TN, Little PJ, Osman N. PDGF beta-receptor kinase activity and ERK1/2 mediate glycosaminoglycan elongation on biglycan and increases binding to LDL. Endocrinology 151: 4356–4367, 2010. doi: 10.1210/en.2010-0027. [DOI] [PubMed] [Google Scholar] · DOI
  63. [63]Gillan L, Matei D, Fishman DA, Gerbin CS, Karlan BY, Chang DD. Periostin secreted by epithelial ovarian carcinoma is a ligand for alpha(V)beta(3) and alpha(V)beta(5) integrins and promotes cell motility. Cancer Res 62: 5358–5364, 2002. [PubMed] [Google Scholar]
  64. [64]Glant TT, Ocsko T, Markovics A, Szekanecz Z, Katz RS, Rauch TA, Mikecz K. Characterization and localization of citrullinated proteoglycan aggrecan in human articular cartilage. PLoS One 11: e0150784, 2016. doi: 10.1371/journal.pone.0150784. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  65. [65]Gopal SK, Greening DW, Zhu HJ, Simpson RJ, Mathias RA. Transformed MDCK cells secrete elevated MMP1 that generates LAMA5 fragments promoting endothelial cell angiogenesis. Sci Rep 6: 28321, 2016. doi: 10.1038/srep28321. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  66. [66]Gottschall PE, Howell MD. ADAMTS expression and function in central nervous system injury and disorders. Matrix Biol 44-46: 70–76, 2015. doi: 10.1016/j.matbio.2015.01.014. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  67. [67]Grande-Allen KJ, Osman N, Ballinger ML, Dadlani H, Marasco S, Little PJ. Glycosaminoglycan synthesis and structure as targets for the prevention of calcific aortic valve disease. Cardiovasc Res 76: 19–28, 2007. doi: 10.1016/j.cardiores.2007.05.014. [DOI] [PubMed] [Google Scholar] · DOI
  68. [68]Grandoch M, Kohlmorgen C, Melchior-Becker A, Feldmann K, Homann S, Müller J, Kiene LS, Zeng-Brouwers J, Schmitz F, Nagy N, Polzin A, Gowert NS, Elvers M, Skroblin P, Yin X, Mayr M, Schaefer L, Tannock LR, Fischer JW. Loss of biglycan enhances thrombin generation in apolipoprotein E-deficient mice: implications for inflammation and atherosclerosis. Arterioscler Thromb Vasc Biol 36: e41–e50, 2016. doi: 10.1161/ATVBAHA.115.306973. [DOI] [PubMed] [Google Scholar] · DOI
  69. [69]Guan J, Liu WQ, Xing MQ, Shi Y, Tan XY, Jiang CQ, Dai HY. Elevated expression of periostin in diabetic cardiomyopathy and the effect of valsartan. BMC Cardiovasc Disord 15: 90, 2015. doi: 10.1186/s12872-015-0084-3. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  70. [70]Halpert I, Sires UI, Roby JD, Potter-Perigo S, Wight TN, Shapiro SD, Welgus HG, Wickline SA, Parks WC. Matrilysin is expressed by lipid-laden macrophages at sites of potential rupture in atherosclerotic lesions and localizes to areas of versican deposition, a proteoglycan substrate for the enzyme. Proc Natl Acad Sci USA 93: 9748–9753, 1996. doi: 10.1073/pnas.93.18.9748. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  71. [71]Harkness LM, Weckmann M, Kopp M, Becker T, Ashton AW, Burgess JK. Tumstatin regulates the angiogenic and inflammatory potential of airway smooth muscle extracellular matrix. J Cell Mol Med 21: 3288–3297, 2017. doi: 10.1111/jcmm.13232. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  72. [72]Hatano S, Kimata K, Hiraiwa N, Kusakabe M, Isogai Z, Adachi E, Shinomura T, Watanabe H. Versican/PG-M is essential for ventricular septal formation subsequent to cardiac atrioventricular cushion development. Glycobiology 22: 1268–1277, 2012. doi: 10.1093/glycob/cws095. [DOI] [PubMed] [Google Scholar] · DOI
  73. [73]Hayward C, Brock DJ. Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies. Hum Mutat 10: 415–423, 1997. doi: 10.1002/(SICI)1098-1004(1997)10:6<415:AID-HUMU1>3.0.CO;2-C. [DOI] [PubMed] [Google Scholar] · DOI
  74. [74]Hayward C, Keston M, Brock DJ, Dietz HC. Fibrillin (FBN1) mutations in Marfan syndrome. Hum Mutat 1: 79, 1992. doi: 10.1002/humu.1380010115. [DOI] [PubMed] [Google Scholar] · DOI
  75. [75]Heegaard AM, Corsi A, Danielsen CC, Nielsen KL, Jorgensen HL, Riminucci M, Young MF, Bianco P. Biglycan deficiency causes spontaneous aortic dissection and rupture in mice. Circulation 115: 2731–2738, 2007. doi: 10.1161/CIRCULATIONAHA.106.653980. [DOI] [PubMed] [Google Scholar] · DOI
  76. [76]Hellenthal FA, Buurman WA, Wodzig WK, Schurink GW. Biomarkers of AAA progression. Part 1: Extracellular matrix degeneration. Nat Rev Cardiol 6: 464–474, 2009. doi: 10.1038/nrcardio.2009.80. [DOI] [PubMed] [Google Scholar] · DOI
  77. [77]Henneton P, Legrand A, Giunta C, Frank M. Arterial fragility in kyphoscoliotic Ehlers-Danlos syndrome. BMJ Case Rep 2018: bcr2018224423, 2018. doi: 10.1136/bcr-2018-224423. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  78. [78]Hirose Y, Chiba K, Karasugi T, Nakajima M, Kawaguchi Y, Mikami Y, Furuichi T, Mio F, Miyake A, Miyamoto T, Ozaki K, Takahashi A, Mizuta H, Kubo T, Kimura T, Tanaka T, Toyama Y, Ikegawa S. A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with lumbar-disc herniation. Am J Hum Genet 82: 1122–1129, 2008. doi: 10.1016/j.ajhg.2008.03.013. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  79. [79]Hu C, Dandapat A, Sun L, Chen J, Marwali MR, Romeo F, Sawamura T, Mehta JL. LOX-1 deletion decreases collagen accumulation in atherosclerotic plaque in low-density lipoprotein receptor knockout mice fed a high-cholesterol diet. Cardiovasc Res 79: 287–293, 2008. doi: 10.1093/cvr/cvn110. [DOI] [PubMed] [Google Scholar] · DOI
  80. [80]Huang J, Davis EC, Chapman SL, Budatha M, Marmorstein LY, Word RA, Yanagisawa H. Fibulin-4 deficiency results in ascending aortic aneurysms: a potential link between abnormal smooth muscle cell phenotype and aneurysm progression. Circ Res 106: 583–592, 2010. doi: 10.1161/CIRCRESAHA.109.207852. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  81. [81]Hucthagowder V, Sausgruber N, Kim KH, Angle B, Marmorstein LY, Urban Z. Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome. Am J Hum Genet 78: 1075–1080, 2006. doi: 10.1086/504304. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  82. [82]Isenberg JS, Hyodo F, Pappan LK, Abu-Asab M, Tsokos M, Krishna MC, Frazier WA, Roberts DD. Blocking thrombospondin-1/CD47 signaling alleviates deleterious effects of aging on tissue responses to ischemia. Arterioscler Thromb Vasc Biol 27: 2582–2588, 2007. doi: 10.1161/ATVBAHA.107.155390. [DOI] [PubMed] [Google Scholar] · DOI
  83. [83]Isenberg JS, Ridnour LA, Dimitry J, Frazier WA, Wink DA, Roberts DD. CD47 is necessary for inhibition of nitric oxide-stimulated vascular cell responses by thrombospondin-1. J Biol Chem 281: 26069–26080, 2006. doi: 10.1074/jbc.M605040200. [DOI] [PubMed] [Google Scholar] · DOI
  84. [84]Isenberg JS, Wink DA, Roberts DD. Thrombospondin-1 antagonizes nitric oxide-stimulated vascular smooth muscle cell responses. Cardiovasc Res 71: 785–793, 2006. doi: 10.1016/j.cardiores.2006.05.024. [DOI] [PubMed] [Google Scholar] · DOI
  85. [85]Iskandar Z, Mordi I, Lang CC, Huang JTJ, Choy AM. Biomarkers of aortopathy in Marfan Syndrome. Cardiol Rev 28: 92–97, 2020. doi: 10.1097/CRD.0000000000000289. [DOI] [PubMed] [Google Scholar] · DOI
  86. [86]Jamaluddin MS, Weakley SM, Yao Q, Chen C. Resistin: functional roles and therapeutic considerations for cardiovascular disease. Br J Pharmacol 165: 622–632, 2012. doi: 10.1111/j.1476-5381.2011.01369.x. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  87. [87]Jaminon A, Reesink K, Kroon A, Schurgers L. The role of vascular smooth muscle cells in arterial remodeling: focus on calcification-related processes. Int J Mol Sci 20: 5694, 2019. doi: 10.3390/ijms20225694. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  88. [88]Jelsig AM, Urban Z, Hucthagowder V, Nissen H, Ousager LB. Novel ELN mutation in a family with supravalvular aortic stenosis and intracranial aneurysm. Eur J Med Genet 60: 110–113, 2017. doi: 10.1016/j.ejmg.2016.11.004. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  89. [89]Jia Y, Wang M, Mao C, Yu F, Wang Y, Xiao R, Jiang C, Zheng L, Xu Q, Zheng M, Fu Y, Hu Q, Kong W. COMP-prohibitin 2 interaction maintains mitochondrial homeostasis and controls smooth muscle cell identity. Cell Death Dis 9: 676, 2018. doi: 10.1038/s41419-018-0703-x. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  90. [90]Jiang W, Zhang Z, Yang H, Lin Q, Qin X. The miR-29b/matrix metalloproteinase 2 axis regulates transdifferentiation and calcification of vascular smooth muscle cells in a calcified environment. Blood Purif. In press. doi: 10.1159/000505571. [DOI] [PubMed] [Google Scholar] · DOI
  91. [91]Jönsson-Rylander AC, Nilsson T, Fritsche-Danielson R, Hammarström A, Behrendt M, Andersson JO, Lindgren K, Andersson AK, Wallbrandt P, Rosengren B, Brodin P, Thelin A, Westin A, Hurt-Camejo E, Lee-Søgaard CH. Role of ADAMTS-1 in atherosclerosis: remodeling of carotid artery, immunohistochemistry, and proteolysis of versican. Arterioscler Thromb Vasc Biol 25: 180–185, 2005. doi: 10.1161/01.ATV.0000150045.27127.37. [DOI] [PubMed] [Google Scholar] · DOI
  92. [92]Jovanovic J, Takagi J, Choulier L, Abrescia NG, Stuart DI, van der Merwe PA, Mardon HJ, Handford PA. αVβ6 is a novel receptor for human fibrillin-1. Comparative studies of molecular determinants underlying integrin-rgd affinity and specificity. J Biol Chem 282: 6743–6751, 2007. doi: 10.1074/jbc.M607008200. [DOI] [PubMed] [Google Scholar] · DOI
  93. [93]Jover E, Silvente A, Marín F, Martínez-González J, Orriols M, Martinez CM, Puche CM, Valdés M, Rodriguez C, Hernández-Romero D. Inhibition of enzymes involved in collagen cross-linking reduces vascular smooth muscle cell calcification. FASEB J 32: 4459–4469, 2018. doi: 10.1096/fj.201700653R. [DOI] [PubMed] [Google Scholar] · DOI
  94. [94]Kalluri R. Basement membranes: structure, assembly and role in tumour angiogenesis. Nat Rev Cancer 3: 422–433, 2003. doi: 10.1038/nrc1094. [DOI] [PubMed] [Google Scholar] · DOI
  95. [95]Kamphaus GD, Colorado PC, Panka DJ, Hopfer H, Ramchandran R, Torre A, Maeshima Y, Mier JW, Sukhatme VP, Kalluri R. Canstatin, a novel matrix-derived inhibitor of angiogenesis and tumor growth. J Biol Chem 275: 1209–1215, 2000. doi: 10.1074/jbc.275.2.1209. [DOI] [PubMed] [Google Scholar] · DOI
  96. [96]Karnik SK, Brooke BS, Bayes-Genis A, Sorensen L, Wythe JD, Schwartz RS, Keating MT, Li DY. A critical role for elastin signaling in vascular morphogenesis and disease. Development 130: 411–423, 2003. doi: 10.1242/dev.00223. [DOI] [PubMed] [Google Scholar] · DOI
  97. [97]Karsdal MA, Henriksen K, Leeming DJ, Woodworth T, Vassiliadis E, Bay-Jensen AC. Novel combinations of Post-Translational Modification (PTM) neo-epitopes provide tissue-specific biochemical markers–are they the cause or the consequence of the disease? Clin Biochem 43: 793–804, 2010. doi: 10.1016/j.clinbiochem.2010.03.015. [DOI] [PubMed] [Google Scholar] · DOI
  98. [98]Katsuda S, Okada Y, Minamoto T, Oda Y, Matsui Y, Nakanishi I. Collagens in human atherosclerosis. Immunohistochemical analysis using collagen type-specific antibodies. Arterioscler Thromb 12: 494–502, 1992. doi: 10.1161/01.ATV.12.4.494. [DOI] [PubMed] [Google Scholar] · DOI
  99. [99]Kaur S, Martin-Manso G, Pendrak ML, Garfield SH, Isenberg JS, Roberts DD. Thrombospondin-1 inhibits VEGF receptor-2 signaling by disrupting its association with CD47. J Biol Chem 285: 38923–38932, 2010. doi: 10.1074/jbc.M110.172304. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
  100. [100]Kelleher CM, McLean SE, Mecham RP. Vascular extracellular matrix and aortic development. Curr Top Dev Biol 62: 153–188, 2004. doi: 10.1016/S0070-2153(04)62006-0. [DOI] [PubMed] [Google Scholar] · DOI
  101. [101]Kennedy J, Jackson G, Ramsden S, Taylor J, Newman W, Wright MJ, Donnai D, Elles R, Briggs MD. COMP mutation screening as an aid for the clinical diagnosis and counselling of patients with a suspected diagnosis of pseudoachondroplasia or multiple epiphyseal dysplasia. Eur J Hum Genet 13: 547–555, 2005. doi: 10.1038/sj.ejhg.5201374. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  102. [102]Kessler T, Zhang L, Liu Z, Yin X, Huang Y, Wang Y, Fu Y, Mayr M, Ge Q, Xu Q, Zhu Y, Wang X, Schmidt K, de Wit C, Erdmann J, Schunkert H, Aherrahrou Z, Kong W. ADAMTS-7 inhibits re-endothelialization of injured arteries and promotes vascular remodeling through cleavage of thrombospondin-1. Circulation 131: 1191–1201, 2015. doi: 10.1161/CIRCULATIONAHA.114.014072. [DOI] [PubMed] [Google Scholar] · DOI
  103. [103]Kim CW, Pokutta-Paskaleva A, Kumar S, Timmins LH, Morris AD, Kang DW, Dalal S, Chadid T, Kuo KM, Raykin J, Li H, Yanagisawa H, Gleason RL Jr, Jo H, Brewster LP. Disturbed flow promotes arterial stiffening through thrombospondin-1. Circulation 136: 1217–1232, 2017. doi: 10.1161/CIRCULATIONAHA.116.026361. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  104. [104]Kinsella MG, Tran PK, Weiser-Evans MC, Reidy M, Majack RA, Wight TN. Changes in perlecan expression during vascular injury: role in the inhibition of smooth muscle cell proliferation in the late lesion. Arterioscler Thromb Vasc Biol 23: 608–614, 2003. doi: 10.1161/01.ATV.0000063109.94810.EE. [DOI] [PubMed] [Google Scholar] · DOI
  105. [105]Kinsella MG, Wight TN. Perlecan: an extracellular matrix heparan sulfate proteoglycan that regulates key events in vascular development and disease. In: Chemistry and Biology of Heparin and Heparan Sulfate, edited by Garg HG, Linhardt RJ, Hales CA. Amsterdam: Elsevier Science, 2005, chapt 22, p. 607–635. [Google Scholar]
  106. [106]Kivirikko KI, Helaakoski T, Tasanen K, Vuori K, Myllylä R, Parkkonen T, Pihlajaniemi T. Molecular biology of prolyl 4-hydroxylase. Ann NY Acad Sci 580: 132–142, 1990. doi: 10.1111/j.1749-6632.1990.tb17925.x. [DOI] [PubMed] [Google Scholar] · DOI
  107. [107]Kojima T, Azar DT, Chang JH. Neostatin-7 regulates bFGF-induced corneal lymphangiogenesis. FEBS Lett 582: 2515–2520, 2008. doi: 10.1016/j.febslet.2008.06.014. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  108. [108]Kontomanolis EN, Kalagasidou S, Pouliliou S, Anthoulaki X, Georgiou N, Papamanolis V, Fasoulakis ZN. The Notch pathway in breast cancer progression. ScientificWorldJournal 2018: 1–11, 2018. doi: 10.1155/2018/2415489. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  109. [109]Koole D, van Herwaarden JA, Schalkwijk CG, Lafeber FPJG, Vink A, Smeets MB, Pasterkamp G, Moll FL. A potential role for glycated cross-links in abdominal aortic aneurysm disease. J Vasc Surg 65: 1493–1503.e3, 2017. doi: 10.1016/j.jvs.2016.04.028. [DOI] [PubMed] [Google Scholar] · DOI
  110. [110]Koskimaki JE, Karagiannis ED, Tang BC, Hammers H, Watkins DN, Pili R, Popel AS. Pentastatin-1, a collagen IV derived 20-mer peptide, suppresses tumor growth in a small cell lung cancer xenograft model. BMC Cancer 10: 29, 2010. doi: 10.1186/1471-2407-10-29. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  111. [111]Kruegel J, Miosge N. Basement membrane components are key players in specialized extracellular matrices. Cell Mol Life Sci 67: 2879–2895, 2010. doi: 10.1007/s00018-010-0367-x. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  112. [112]Kubota K, Okazaki J, Louie O, Kent KC, Liu B. TGF-beta stimulates collagen (I) in vascular smooth muscle cells via a short element in the proximal collagen promoter. J Surg Res 109: 43–50, 2003. doi: 10.1016/S0022-4804(02)00037-9. [DOI] [PubMed] [Google Scholar] · DOI
  113. [113]Kuivaniemi H, Tromp G, Prockop DJ. Genetic causes of aortic aneurysms. Unlearning at least part of what the textbooks say. J Clin Invest 88: 1441–1444, 1991. doi: 10.1172/JCI115452. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  114. [114]Kumar J, Yumnam S, Basu T, Ghosh A, Garg G, Karthikeyan G, Sengupta S. Association of polymorphisms in 9p21 region with CAD in North Indian population: replication of SNPs identified through GWAS. Clin Genet 79: 588–593, 2011. doi: 10.1111/j.1399-0004.2010.01509.x. [DOI] [PubMed] [Google Scholar] · DOI
  115. [115]Kunjathoor VV, Chiu DS, O’Brien KD, LeBoeuf RC. Accumulation of biglycan and perlecan, but not versican, in lesions of murine models of atherosclerosis. Arterioscler Thromb Vasc Biol 22: 462–468, 2002. doi: 10.1161/hq0302.105378. [DOI] [PubMed] [Google Scholar] · DOI
  116. [116]Kuzan A, Michel O, Gamian A. Glycation of matrix proteins in the artery inhibits migration of smooth muscle cells from the media to the intima. Folia Biol (Praha) 63: 105–114, 2017. [DOI] [PubMed] [Google Scholar]
  117. [117]Kyriakides TR, Maclauchlan S. The role of thrombospondins in wound healing, ischemia, and the foreign body reaction. J Cell Commun Signal 3: 215–225, 2009. doi: 10.1007/s12079-009-0077-z. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  118. [118]Kyriakides TR, Rojnuckarin P, Reidy MA, Hankenson KD, Papayannopoulou T, Kaushansky K, Bornstein P. Megakaryocytes require thrombospondin-2 for normal platelet formation and function. Blood 101: 3915–3923, 2003. doi: 10.1182/blood.V101.10.3915. [DOI] [PubMed] [Google Scholar] · DOI
  119. [119]Kyriakides TR, Zhu YH, Smith LT, Bain SD, Yang Z, Lin MT, Danielson KG, Iozzo RV, LaMarca M, McKinney CE, Ginns EI, Bornstein P. Mice that lack thrombospondin 2 display connective tissue abnormalities that are associated with disordered collagen fibrillogenesis, an increased vascular density, and a bleeding diathesis. J Cell Biol 140: 419–430, 1998. doi: 10.1083/jcb.140.2.419. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  120. [120]Landry NM, Cohen S, Dixon IMC. Periostin in cardiovascular disease and development: a tale of two distinct roles. Basic Res Cardiol 113: 1, 2017. doi: 10.1007/s00395-017-0659-5. [DOI] [PubMed] [Google Scholar] · DOI
  121. [121]LaVoie MJ, Selkoe DJ. The Notch ligands, Jagged and Delta, are sequentially processed by alpha-secretase and presenilin/gamma-secretase and release signaling fragments. J Biol Chem 278: 34427–34437, 2003. doi: 10.1074/jbc.M302659200. [DOI] [PubMed] [Google Scholar] · DOI
  122. [122]Le VP, Knutsen RH, Mecham RP, Wagenseil JE. Decreased aortic diameter and compliance precedes blood pressure increases in postnatal development of elastin-insufficient mice. Am J Physiol Heart Circ Physiol 301: H221–H229, 2011. doi: 10.1152/ajpheart.00119.2011. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  123. [123]Lee NV, Sato M, Annis DS, Loo JA, Wu L, Mosher DF, Iruela-Arispe ML. ADAMTS1 mediates the release of antiangiogenic polypeptides from TSP1 and 2. EMBO J 25: 5270–5283, 2006. doi: 10.1038/sj.emboj.7601400. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  124. [124]Leeming D, He Y, Veidal S, Nguyen Q, Larsen D, Koizumi M, Segovia-Silvestre T, Zhang C, Zheng Q, Sun S, Cao Y, Barkholt V, Hägglund P, Bay-Jensen A, Qvist P, Karsdal M. A novel marker for assessment of liver matrix remodeling: an enzyme-linked immunosorbent assay (ELISA) detecting a MMP generated type I collagen neo-epitope (C1M). Biomarkers 16: 616–628, 2011. doi: 10.3109/1354750X.2011.620628. [DOI] [PubMed] [Google Scholar] · DOI
  125. [125]Li DY, Brooke B, Davis EC, Mecham RP, Sorensen LK, Boak BB, Eichwald E, Keating MT. Elastin is an essential determinant of arterial morphogenesis. Nature 393: 276–280, 1998. doi: 10.1038/30522. [DOI] [PubMed] [Google Scholar] · DOI
  126. [126]Li G, Oparil S, Sanders JM, Zhang L, Dai M, Chen LB, Conway SJ, McNamara CA, Sarembock IJ. Phosphatidylinositol-3-kinase signaling mediates vascular smooth muscle cell expression of periostin in vivo and in vitro. Atherosclerosis 188: 292–300, 2006. doi: 10.1016/j.atherosclerosis.2005.11.002. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  127. [127]Li Q, Olsen BR. Increased angiogenic response in aortic explants of collagen XVIII/endostatin-null mice. Am J Pathol 165: 415–424, 2004. doi: 10.1016/S0002-9440(10)63307-X. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  128. [128]Liang Y, Fu Y, Qi R, Wang M, Yang N, He L, Yu F, Zhang J, Yun CH, Wang X, Liu J, Kong W. Cartilage oligomeric matrix protein is a natural inhibitor of thrombin. Blood 126: 905–914, 2015. doi: 10.1182/blood-2015-01-621292. [DOI] [PubMed] [Google Scholar] · DOI
  129. [129]Lin Y, Chen H, Wang Y, Jin C, Lin X, Wang C, Lu Y, Chen Z, Wang JA, Xiang M. Association of serum ADAMTS7 levels and genetic variant rs1994016 with acute coronary syndrome in a Chinese population: A case control study. Atherosclerosis 275: 312–318, 2018. doi: 10.1016/j.atherosclerosis.2018.06.872. [DOI] [PubMed] [Google Scholar] · DOI
  130. [130]Liu T, Lin J, Ju T, Chu L, Zhang L. Vascular smooth muscle cell differentiation to an osteogenic phenotype involves matrix metalloproteinase-2 modulation by homocysteine. Mol Cell Biochem 406: 139–149, 2015. doi: 10.1007/s11010-015-2432-0. [DOI] [PubMed] [Google Scholar] · DOI
  131. [131]Liu X, Wu H, Byrne M, Krane S, Jaenisch R. Type III collagen is crucial for collagen I fibrillogenesis and for normal cardiovascular development. Proc Natl Acad Sci USA 94: 1852–1856, 1997. doi: 10.1073/pnas.94.5.1852. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
  132. [132]Liu Z, Morgan S, Ren J, Wang Q, Annis DS, Mosher DF, Zhang J, Sorenson CM, Sheibani N, Liu B. Thrombospondin-1 (TSP1) contributes to the development of vascular inflammation by regulating monocytic cell motility in mouse models of abdominal aortic aneurysm. Circ Res 117: 129–141, 2015. doi: 10.1161/CIRCRESAHA.117.305262. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  133. [133]Löhler J, Timpl R, Jaenisch R. Embryonic lethal mutation in mouse collagen I gene causes rupture of blood vessels and is associated with erythropoietic and mesenchymal cell death. Cell 38: 597–607, 1984. doi: 10.1016/0092-8674(84)90514-2. [DOI] [PubMed] [Google Scholar] · DOI
  134. [134]Lord MS, Chuang CY, Melrose J, Davies MJ, Iozzo RV, Whitelock JM. The role of vascular-derived perlecan in modulating cell adhesion, proliferation and growth factor signaling. Matrix Biol 35: 112–122, 2014. doi: 10.1016/j.matbio.2014.01.016. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
  135. [135]Lotery AJ, Baas D, Ridley C, Jones RP, Klaver CC, Stone E, Nakamura T, Luff A, Griffiths H, Wang T, Bergen AA, Trump D. Reduced secretion of fibulin 5 in age-related macular degeneration and cutis laxa. Hum Mutat 27: 568–574, 2006. doi: 10.1002/humu.20344. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  136. [136]Lu P, Takai K, Weaver VM, Werb Z. Extracellular matrix degradation and remodeling in development and disease. Cold Spring Harb Perspect Biol 3: a005058, 2011. doi: 10.1101/cshperspect.a005058. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
  137. [137]Luque A, Carpizo DR, Iruela-Arispe ML. ADAMTS1/METH1 inhibits endothelial cell proliferation by direct binding and sequestration of VEGF165. J Biol Chem 278: 23656–23665, 2003. doi: 10.1074/jbc.M212964200. [DOI] [PubMed] [Google Scholar] · DOI
  138. [138]Lynch M, Barallobre-Barreiro J, Jahangiri M, Mayr M. Vascular proteomics in metabolic and cardiovascular diseases. J Intern Med 280: 325–338, 2016. doi: 10.1111/joim.12486. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  139. [139]Ma B, Yao F, Xie N, Mao C, Liu F, Gong Z, Zhao G, Liu Z, Cai Z, Yu F, Dai R, Chen Z, Wang L, Xu Q, Kong W, Fu Y. Cartilage oligomeric matrix protein is a novel notch ligand driving embryonic stem cell differentiation towards the smooth muscle lineage. J Mol Cell Cardiol 121: 69–80, 2018. doi: 10.1016/j.yjmcc.2018.07.002. [DOI] [PubMed] [Google Scholar] · DOI
  140. [141]Mao JR, Bristow J. The Ehlers-Danlos syndrome: on beyond collagens. J Clin Invest 107: 1063–1069, 2001. doi: 10.1172/JCI12881. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
  141. [142]Maquart FX, Siméon A, Pasco S, Monboisse JC. [Regulation of cell activity by the extracellular matrix: the concept of matrikines]. J Soc Biol 193: 423–428, 1999. doi: 10.1051/jbio/1999193040423. [DOI] [PubMed] [Google Scholar] · DOI
  142. [144]Martínez-Revelles S, García-Redondo AB, Avendaño MS, Varona S, Palao T, Orriols M, Roque FR, Fortuño A, Touyz RM, Martínez-González J, Salaices M, Rodríguez C, Briones AM. Lysyl oxidase induces vascular oxidative stress and contributes to arterial stiffness and abnormal elastin structure in hypertension: role of p38MAPK. Antioxid Redox Signal 27: 379–397, 2017. doi: 10.1089/ars.2016.6642. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  143. [145]Martinez JR, Dhawan A, Farach-Carson MC. Modular proteoglycan perlecan/HSPG2: mutations, phenotypes, and functions. Genes (Basel) 9: 556, 2018. doi: 10.3390/genes9110556. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  144. [146]Matsumoto T, Abe H, Ohashi T, Kato Y, Sato M. Local elastic modulus of atherosclerotic lesions of rabbit thoracic aortas measured by pipette aspiration method. Physiol Meas 23: 635–648, 2002. doi: 10.1088/0967-3334/23/4/304. [DOI] [PubMed] [Google Scholar] · DOI
  145. [147]Maurice P, Blaise S, Gayral S, Debelle L, Laffargue M, Hornebeck W, Duca L. Elastin fragmentation and atherosclerosis progression: the elastokine concept. Trends Cardiovasc Med 23: 211–221, 2013. doi: 10.1016/j.tcm.2012.12.004. [DOI] [PubMed] [Google Scholar] · DOI
  146. [148]McLaughlin PJ, Chen Q, Horiguchi M, Starcher BC, Stanton JB, Broekelmann TJ, Marmorstein AD, McKay B, Mecham R, Nakamura T, Marmorstein LY. Targeted disruption of fibulin-4 abolishes elastogenesis and causes perinatal lethality in mice. Mol Cell Biol 26: 1700–1709, 2006. doi: 10.1128/MCB.26.5.1700-1709.2006. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  147. [149]Meester JA, Vandeweyer G, Pintelon I, Lammens M, Van Hoorick L, De Belder S, Waitzman K, Young L, Markham LW, Vogt J, Richer J, Beauchesne LM, Unger S, Superti-Furga A, Prsa M, Dhillon R, Reyniers E, Dietz HC, Wuyts W, Mortier G, Verstraeten A, Van Laer L, Loeys BL. Loss-of-function mutations in the X-linked biglycan gene cause a severe syndromic form of thoracic aortic aneurysms and dissections. Genet Med 19: 386–395, 2017. doi: 10.1038/gim.2016.126. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  148. [150]Merrilees MJ, Lemire JM, Fischer JW, Kinsella MG, Braun KR, Clowes AW, Wight TN. Retrovirally mediated overexpression of versican v3 by arterial smooth muscle cells induces tropoelastin synthesis and elastic fiber formation in vitro and in neointima after vascular injury. Circ Res 90: 481–487, 2002. doi: 10.1161/hh0402.105791. [DOI] [PubMed] [Google Scholar] · DOI
  149. [151]Mikael LR, de Paiva AMG, Gomes MM, Sousa ALL, Jardim PCBV, Vitorino PVO, Euzébio MB, Sousa WM, Barroso WKS. Vascular aging and arterial stiffness. Arq Bras Cardiol 109: 253–258, 2017. doi: 10.5935/abc.20170091. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  150. [152]Miller TW, Isenberg JS, Roberts DD. Thrombospondin-1 is an inhibitor of pharmacological activation of soluble guanylate cyclase. Br J Pharmacol 159: 1542–1547, 2010. doi: 10.1111/j.1476-5381.2009.00631.x. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  151. [153]Miyamoto T, Inoue H, Sakamoto Y, Kudo E, Naito T, Mikawa T, Mikawa Y, Isashiki Y, Osabe D, Shinohara S, Shiota H, Itakura M. Identification of a novel splice site mutation of the CSPG2 gene in a Japanese family with Wagner syndrome. Invest Ophthalmol Vis Sci 46: 2726–2735, 2005. doi: 10.1167/iovs.05-0057. [DOI] [PubMed] [Google Scholar] · DOI
  152. [154]Mizuno K, Boudko S, Engel J, Bächinger HP. Vascular Ehlers-Danlos syndrome mutations in type III collagen differently stall the triple helical folding. J Biol Chem 288: 19166–19176, 2013. doi: 10.1074/jbc.M113.462002. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  153. [155]Morla AO, Mogford JE. Control of smooth muscle cell proliferation and phenotype by integrin signaling through focal adhesion kinase. Biochem Biophys Res Commun 272: 298–302, 2000. doi: 10.1006/bbrc.2000.2769. [DOI] [PubMed] [Google Scholar] · DOI
  154. [156]Moura R, Tjwa M, Vandervoort P, Van Kerckhoven S, Holvoet P, Hoylaerts MF. Thrombospondin-1 deficiency accelerates atherosclerotic plaque maturation in ApoE−/− mice. Circ Res 103: 1181–1189, 2008. doi: 10.1161/CIRCRESAHA.108.185645. [DOI] [PubMed] [Google Scholar] · DOI
  155. [157]Muppala S, Frolova E, Xiao R, Krukovets I, Yoon S, Hoppe G, Vasanji A, Plow E, Stenina-Adognravi O. Proangiogenic Properties of Thrombospondin-4. Arterioscler Thromb Vasc Biol 35: 1975–1986, 2015. doi: 10.1161/ATVBAHA.115.305912. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  156. [158]Nakamura T, Lozano PR, Ikeda Y, Iwanaga Y, Hinek A, Minamisawa S, Cheng CF, Kobuke K, Dalton N, Takada Y, Tashiro K, Ross J Jr, Honjo T, Chien KR. Fibulin-5/DANCE is essential for elastogenesis in vivo. Nature 415: 171–175, 2002. doi: 10.1038/415171a. [DOI] [PubMed] [Google Scholar] · DOI
  157. [159]Nakamura T, Ruiz-Lozano P, Lindner V, Yabe D, Taniwaki M, Furukawa Y, Kobuke K, Tashiro K, Lu Z, Andon NL, Schaub R, Matsumori A, Sasayama S, Chien KR, Honjo T. DANCE, a novel secreted RGD protein expressed in developing, atherosclerotic, and balloon-injured arteries. J Biol Chem 274: 22476–22483, 1999. doi: 10.1074/jbc.274.32.22476. [DOI] [PubMed] [Google Scholar] · DOI
  158. [160]Narizhneva NV, Razorenova OV, Podrez EA, Chen J, Chandrasekharan UM, DiCorleto PE, Plow EF, Topol EJ, Byzova TV. Thrombospondin-1 up-regulates expression of cell adhesion molecules and promotes monocyte binding to endothelium. FASEB J 19: 1158–1160, 2005. doi: 10.1096/fj.04-3310fje. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  159. [161]Neptune ER, Frischmeyer PA, Arking DE, Myers L, Bunton TE, Gayraud B, Ramirez F, Sakai LY, Dietz HC. Dysregulation of TGF-beta activation contributes to pathogenesis in Marfan syndrome. Nat Genet 33: 407–411, 2003. doi: 10.1038/ng1116. [DOI] [PubMed] [Google Scholar] · DOI
  160. [162]Novelli EM, Little-Ihrig L, Knupp HE, Rogers NM, Yao M, Baust JJ, Meijles D, St Croix CM, Ross MA, Pagano PJ, DeVallance ER, Miles G, Potoka KP, Isenberg JS, Gladwin MT. Vascular TSP1-CD47 signaling promotes sickle cell-associated arterial vasculopathy and pulmonary hypertension in mice. Am J Physiol Lung Cell Mol Physiol 316: L1150–L1164, 2019. doi: 10.1152/ajplung.00302.2018. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  161. [163]O’Brien KD, Olin KL, Alpers CE, Chiu W, Ferguson M, Hudkins K, Wight TN, Chait A. Comparison of apolipoprotein and proteoglycan deposits in human coronary atherosclerotic plaques: colocalization of biglycan with apolipoproteins. Circulation 98: 519–527, 1998. doi: 10.1161/01.CIR.98.6.519. [DOI] [PubMed] [Google Scholar] · DOI
  162. [165]Okada M, Murata N, Yamawaki H. Canstatin stimulates migration of rat cardiac fibroblasts via secretion of matrix metalloproteinase-2. Am J Physiol Cell Physiol 312: C199–C208, 2017. doi: 10.1152/ajpcell.00329.2015. [DOI] [PubMed] [Google Scholar] · DOI
  163. [166]Olin KL, Potter-Perigo S, Barrett PH, Wight TN, Chait A. Lipoprotein lipase enhances the binding of native and oxidized low density lipoproteins to versican and biglycan synthesized by cultured arterial smooth muscle cells. J Biol Chem 274: 34629–34636, 1999. doi: 10.1074/jbc.274.49.34629. [DOI] [PubMed] [Google Scholar] · DOI
  164. [167]Olsen I, Singhrao SK, Potempa J. Citrullination as a plausible link to periodontitis, rheumatoid arthritis, atherosclerosis and Alzheimer’s disease. J Oral Microbiol 10: 1487742, 2018. doi: 10.1080/20002297.2018.1487742. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  165. [168]Olsson U, Ostergren-Lundén G, Moses J. Glycosaminoglycan-lipoprotein interaction. Glycoconj J 18: 789–797, 2001. doi: 10.1023/A:1021155518464. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  166. [169]Orr AW, Lee MY, Lemmon JA, Yurdagul A Jr, Gomez MF, Bortz PD, Wamhoff BR. Molecular mechanisms of collagen isotype-specific modulation of smooth muscle cell phenotype. Arterioscler Thromb Vasc Biol 29: 225–231, 2009. doi: 10.1161/ATVBAHA.108.178749. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  167. [170]Palao T, Rippe C, van Veen H, VanBavel E, Swärd K, Bakker EN. Thrombospondin-4 knockout in hypertension protects small-artery endothelial function but induces aortic aneurysms. Am J Physiol Heart Circ Physiol 310: H1486–H1493, 2016. doi: 10.1152/ajpheart.00046.2016. [DOI] [PubMed] [Google Scholar] · DOI
  168. [171]Park J, Scherer PE. Adipocyte-derived endotrophin promotes malignant tumor progression. J Clin Invest 122: 4243–4256, 2012. doi: 10.1172/JCI63930. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
  169. [172]Pereira L, Andrikopoulos K, Tian J, Lee SY, Keene DR, Ono R, Reinhardt DP, Sakai LY, Biery NJ, Bunton T, Dietz HC, Ramirez F. Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome. Nat Genet 17: 218–222, 1997. doi: 10.1038/ng1097-218. [DOI] [PubMed] [Google Scholar] · DOI
  170. [173]Pillarisetti S, Paka L, Obunike JC, Berglund L, Goldberg IJ. Subendothelial retention of lipoprotein (a). Evidence that reduced heparan sulfate promotes lipoprotein binding to subendothelial matrix. J Clin Invest 100: 867–874, 1997. doi: 10.1172/JCI119602. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  171. [174]Pohjolainen V, Mustonen E, Taskinen P, Näpänkangas J, Leskinen H, Ohukainen P, Peltonen T, Aro J, Juvonen T, Satta J, Ruskoaho H, Rysä J. Increased thrombospondin-2 in human fibrosclerotic and stenotic aortic valves. Atherosclerosis 220: 66–71, 2012. doi: 10.1016/j.atherosclerosis.2011.10.003. [DOI] [PubMed] [Google Scholar] · DOI
  172. [175]Pokidysheva E, Boudko S, Vranka J, Zientek K, Maddox K, Moser M, Fässler R, Ware J, Bächinger HP. Biological role of prolyl 3-hydroxylation in type IV collagen. Proc Natl Acad Sci USA 111: 161–166, 2014. doi: 10.1073/pnas.1307597111. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  173. [176]Pöschl E, Schlötzer-Schrehardt U, Brachvogel B, Saito K, Ninomiya Y, Mayer U. Collagen IV is essential for basement membrane stability but dispensable for initiation of its assembly during early development. Development 131: 1619–1628, 2004. doi: 10.1242/dev.01037. [DOI] [PubMed] [Google Scholar] · DOI
  174. [177]Prado AF, Pernomian L, Azevedo A, Costa RAP, Rizzi E, Ramos J, Paes Leme AF, Bendhack LM, Tanus-Santos JE, Gerlach RF. Matrix metalloproteinase-2-induced epidermal growth factor receptor transactivation impairs redox balance in vascular smooth muscle cells and facilitates vascular contraction. Redox Biol 18: 181–190, 2018. doi: 10.1016/j.redox.2018.07.005. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  175. [178]Pyeritz RE, McKusick VA. The Marfan syndrome: diagnosis and management. N Engl J Med 300: 772–777, 1979. doi: 10.1056/NEJM197904053001406. [DOI] [PubMed] [Google Scholar] · DOI
  176. [179]Qin W, Cao Y, Li L, Chen W, Chen X. Upregulation of ADAMTS-7 and downregulation of COMP are associated with aortic aneurysm. Mol Med Rep 16: 5459–5463, 2017. doi: 10.3892/mmr.2017.7293. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  177. [180]Rabie T, Strehl A, Ludwig A, Nieswandt B. Evidence for a role of ADAM17 (TACE) in the regulation of platelet glycoprotein V. J Biol Chem 280: 14462–14468, 2005. doi: 10.1074/jbc.M500041200. [DOI] [PubMed] [Google Scholar] · DOI
  178. [181]Rauch U, Saxena A, Lorkowski S, Rauterberg J, Björkbacka H, Durbeej M, Hultgårdh-Nilsson A. Laminin isoforms in atherosclerotic arteries from mice and man. Histol Histopathol 26: 711–724, 2011. doi: 10.14670/HH-26.711. [DOI] [PubMed] [Google Scholar] · DOI
  179. [182]Rebustini IT, Myers C, Lassiter KS, Surmak A, Szabova L, Holmbeck K, Pedchenko V, Hudson BG, Hoffman MP. MT2-MMP-dependent release of collagen IV NC1 domains regulates submandibular gland branching morphogenesis. Dev Cell 17: 482–493, 2009. doi: 10.1016/j.devcel.2009.07.016. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  180. [183]Reilly MP, Li M, He J, Ferguson JF, Stylianou IM, Mehta NN, Burnett MS, Devaney JM, Knouff CW, Thompson JR, Horne BD, Stewart AF, Assimes TL, Wild PS, Allayee H, Nitschke PL, Patel RS, Martinelli N, Girelli D, Quyyumi AA, Anderson JL, Erdmann J, Hall AS, Schunkert H, Quertermous T, Blankenberg S, Hazen SL, Roberts R, Kathiresan S, Samani NJ, Epstein SE, Rader DJ; Myocardial Infarction Genetics Consortium; Wellcome Trust Case Control Consortium . Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. Lancet 377: 383–392, 2011. doi: 10.1016/S0140-6736(10)61996-4. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  181. [184]Rekhter MD. Collagen synthesis in atherosclerosis: too much and not enough. Cardiovasc Res 41: 376–384, 1999. doi: 10.1016/S0008-6363(98)00321-6. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  182. [185]Ren P, Hughes M, Krishnamoorthy S, Zou S, Zhang L, Wu D, Zhang C, Curci JA, Coselli JS, Milewicz DM, LeMaire SA, Shen YH. Critical role of ADAMTS-4 in the development of sporadic aortic aneurysm and dissection in mice. Sci Rep 7: 12351, 2017. doi: 10.1038/s41598-017-12248-z. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  183. [186]Rhodes JM, Simons M. The extracellular matrix and blood vessel formation: not just a scaffold. J Cell Mol Med 11: 176–205, 2007. doi: 10.1111/j.1582-4934.2007.00031.x. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  184. [187]Ribeiro SM, Poczatek M, Schultz-Cherry S, Villain M, Murphy-Ullrich JE. The activation sequence of thrombospondin-1 interacts with the latency-associated peptide to regulate activation of latent transforming growth factor-beta. J Biol Chem 274: 13586–13593, 1999. doi: 10.1074/jbc.274.19.13586. [DOI] [PubMed] [Google Scholar] · DOI
  185. [188]Ricard-Blum S, Vallet SD. Fragments generated upon extracellular matrix remodeling: Biological regulators and potential drugs. Matrix Biol 75–76: 170–189, 2019. doi: 10.1016/j.matbio.2017.11.005. [DOI] [PubMed] [Google Scholar] · DOI
  186. [189]Riessen R, Isner JM, Blessing E, Loushin C, Nikol S, Wight TN. Regional differences in the distribution of the proteoglycans biglycan and decorin in the extracellular matrix of atherosclerotic and restenotic human coronary arteries. Am J Pathol 144: 962–974, 1994. [PMC free article] [PubMed] [Google Scholar]
  187. [190]Rogers NM, Sharifi-Sanjani M, Yao M, Ghimire K, Bienes-Martinez R, Mutchler SM, Knupp HE, Baust J, Novelli EM, Ross M, St Croix C, Kutten JC, Czajka CA, Sembrat JC, Rojas M, Labrousse-Arias D, Bachman TN, Vanderpool RR, Zuckerbraun BS, Champion HC, Mora AL, Straub AC, Bilonick RA, Calzada MJ, Isenberg JS. TSP1-CD47 signaling is upregulated in clinical pulmonary hypertension and contributes to pulmonary arterial vasculopathy and dysfunction. Cardiovasc Res 113: 15–29, 2017. doi: 10.1093/cvr/cvw218. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  188. [191]Rosenbloom J, Cywinski A. Inhibition of proline hydroxylation does not inhibit secretion of tropoelastin by chick aorta cells. FEBS Lett 65: 246–250, 1976. doi: 10.1016/0014-5793(76)80490-5. [DOI] [PubMed] [Google Scholar] · DOI
  189. [192]Rundhaug JE. Matrix metalloproteinases and angiogenesis. J Cell Mol Med 9: 267–285, 2005. doi: 10.1111/j.1582-4934.2005.tb00355.x. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  190. [193]Santhanam L, Tuday EC, Webb AK, Dowzicky P, Kim JH, Oh YJ, Sikka G, Kuo M, Halushka MK, Macgregor AM, Dunn J, Gutbrod S, Yin D, Shoukas A, Nyhan D, Flavahan NA, Belkin AM, Berkowitz DE. Decreased S-nitrosylation of tissue transglutaminase contributes to age-related increases in vascular stiffness. Circ Res 107: 117–125, 2010. doi: 10.1161/CIRCRESAHA.109.215228. [DOI] [PubMed] [Google Scholar] · DOI
  191. [194]Schmitt M. Versican vs versikine: tolerance vs attack. Blood 128: 612–613, 2016. doi: 10.1182/blood-2016-06-721092. [DOI] [PubMed] [Google Scholar] · DOI
  192. [195]Schultz-Cherry S, Chen H, Mosher DF, Misenheimer TM, Krutzsch HC, Roberts DD, Murphy-Ullrich JE. Regulation of transforming growth factor-beta activation by discrete sequences of thrombospondin 1. J Biol Chem 270: 7304–7310, 1995. doi: 10.1074/jbc.270.13.7304. [DOI] [PubMed] [Google Scholar] · DOI
  193. [196]Schultz-Cherry S, Lawler J, Murphy-Ullrich JE. The type 1 repeats of thrombospondin 1 activate latent transforming growth factor-beta. J Biol Chem 269: 26783–26788, 1994. [PubMed] [Google Scholar]
  194. [197]Schulz B, Pruessmeyer J, Maretzky T, Ludwig A, Blobel CP, Saftig P, Reiss K. ADAM10 regulates endothelial permeability and T-Cell transmigration by proteolysis of vascular endothelial cadherin. Circ Res 102: 1192–1201, 2008. doi: 10.1161/CIRCRESAHA.107.169805. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  195. [198]Schunkert H, König IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, Preuss M, Stewart AF, Barbalic M, Gieger C, Absher D, Aherrahrou Z, Allayee H, Altshuler D, Anand SS, Andersen K, Anderson JL, Ardissino D, Ball SG, Balmforth AJ, Barnes TA, Becker DM, Becker LC, Berger K, Bis JC, Boekholdt SM, Boerwinkle E, Braund PS, Brown MJ, Burnett MS, Buysschaert I, Cardiogenics; Carlquist JF, Chen L, Cichon S, Codd V, Davies RW, Dedoussis G, Dehghan A, Demissie S, Devaney JM, Diemert P, Do R, Doering A, Eifert S, Mokhtari NE, Ellis SG, Elosua R, Engert JC, Epstein SE, de Faire U, Fischer M, Folsom AR, Freyer J, Gigante B, Girelli D, Gretarsdottir S, Gudnason V, Gulcher JR, Halperin E, Hammond N, Hazen SL, Hofman A, Horne BD, Illig T, Iribarren C, Jones GT, Jukema JW, Kaiser MA, Kaplan LM, Kastelein JJ, Khaw KT, Knowles JW, Kolovou G, Kong A, Laaksonen R, Lambrechts D, Leander K, Lettre G, Li M, Lieb W, Loley C, Lotery AJ, Mannucci PM, Maouche S, Martinelli N, McKeown PP, Meisinger C, Meitinger T, Melander O, Merlini PA, Mooser V, Morgan T, Mühleisen TW, Muhlestein JB, Münzel T, Musunuru K, Nahrstaedt J, Nelson CP, Nöthen MM, Olivieri O, Patel RS, Patterson CC, Peters A, Peyvandi F, Qu L, Quyyumi AA, Rader DJ, Rallidis LS, Rice C, Rosendaal FR, Rubin D, Salomaa V, Sampietro ML, Sandhu MS, Schadt E, Schäfer A, Schillert A, Schreiber S, Schrezenmeir J, Schwartz SM, Siscovick DS, Sivananthan M, Sivapalaratnam S, Smith A, Smith TB, Snoep JD, Soranzo N, Spertus JA, Stark K, Stirrups K, Stoll M, Tang WH, Tennstedt S, Thorgeirsson G, Thorleifsson G, Tomaszewski M, Uitterlinden AG, van Rij AM, Voight BF, Wareham NJ, Wells GA, Wichmann HE, Wild PS, Willenborg C, Witteman JC, Wright BJ, Ye S, Zeller T, Ziegler A, Cambien F, Goodall AH, Cupples LA, Quertermous T, März W, Hengstenberg C, Blankenberg S, Ouwehand WH, Hall AS, Deloukas P, Thompson JR, Stefansson K, Roberts R, Thorsteinsdottir U, O’Donnell CJ, McPherson R, Erdmann J; CARDIoGRAM Consortium . Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 43: 333–338, 2011. doi: 10.1038/ng.784. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
  196. [199]Schurgers LJ, Spronk HM, Skepper JN, Hackeng TM, Shanahan CM, Vermeer C, Weissberg PL, Proudfoot D. Post-translational modifications regulate matrix Gla protein function: importance for inhibition of vascular smooth muscle cell calcification. J Thromb Haemost 5: 2503–2511, 2007. doi: 10.1111/j.1538-7836.2007.02758.x. [DOI] [PubMed] [Google Scholar] · DOI
  197. [200]Segev A, Nili N, Strauss BH. The role of perlecan in arterial injury and angiogenesis. Cardiovasc Res 63: 603–610, 2004. doi: 10.1016/j.cardiores.2004.03.028. [DOI] [PubMed] [Google Scholar] · DOI
  198. [201]Segovia-Silvestre T, Reichenbach V, Fernández-Varo G, Vassiliadis E, Barascuk N, Morales-Ruiz M, Karsdal MA, Jiménez W. Circulating CO3-610, a degradation product of collagen III, closely reflects liver collagen and portal pressure in rats with fibrosis. Fibrogenesis Tissue Repair 4: 19, 2011. doi: 10.1186/1755-1536-4-19. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  199. [202]Sehgel NL, Vatner SF, Meininger GA. “Smooth muscle cell stiffness syndrome”-Revisiting the structural basis of arterial stiffness. Front Physiol 6: 335, 2015. doi: 10.3389/fphys.2015.00335. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  200. [203]Shen Z, Yao C, Wang Z, Yue L, Fang Z, Yao H, Lin F, Zhao H, Sun YJ, Bian XW, Jiang W, Wang X, Li Y, Lu G, Poon WS, Kung HF, Lin MC. Vastatin, an endogenous antiangiogenesis polypeptide that is lost in hepatocellular carcinoma, effectively inhibits tumor metastasis. Mol Ther 24: 1358–1368, 2016. doi: 10.1038/mt.2016.56. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI

200 of 239 shown

Cited by

Sorted by citations

Authors
Ma, Z., Mao, C., Jia, Y., Fu, Y., & Kong, W.
Affiliations
Peking University (CN)
Corresponding author
Fu, Yi
Venue
American Journal of Physiology-Cell Physiology
Published
2020-09-01
Volume
319
Issue
3
Pages
C481-C499
ISSN
  • 0363-6143 (ISSN-L)
  • 1522-1563
OpenAlex
W3037400185
Cited by
129
References
5
Citations by year
2026: 16 · 2025: 26 · 2024: 20 · 2023: 27 · 2022: 26 · 2021: 12 · 2020: 2
FWCI
1.95
Type
journal article
Language
en
Open access
Locations
  • American Journal of Physiology-Cell Physiology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Natural Science Foundation of China (81730010, 91839302, 81922009, 91739116, 81921001, 31930056)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Protease and Inhibitor Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
Keywords
vascular remodeling, extracellular matrix, matrix metalloproteinases, extracellular matrix degradation, post-translational modification, vascular disease, aging, biomarkers, therapeutic target
MeSH terms
Animals, Extracellular Matrix, Humans, Vascular Diseases, Biomarkers, Extracellular Matrix Proteins, Matrix Metalloproteinases, Vascular Remodeling

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review