Cell-Seeded Biomaterial Scaffolds: The Urgent Need for Unanswered Accelerated Angiogenesis
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One of the most arduous challenges in tissue engineering is neovascularization, without which there is a lack of nutrients delivered to a target tissue. Angiogenesis should be completed at an optimal density and within an appropriate period of time to prevent cell necrosis. Failure to meet this challenge brings about poor functionality for the tissue in comparison with the native tissue, extensively reducing cell viability. Prior studies devoted to angiogenesis have provided researchers with some biomaterial scaffolds and cell choices for angiogenesis. For example, while most current angiogenesis approaches require a variety of stimulatory factors ranging from biomechanical to biomolecular to cellular, some other promising stimulatory factors have been underdeveloped (such as electrical, topographical, and magnetic). When it comes to choosing biomaterial scaffolds in tissue engineering for angiogenesis, key traits rush to mind including biocompatibility, appropriate physical and mechanical properties (adhesion strength, shear stress, and malleability), as well as identifying the appropriate biomaterial in terms of stability and degradation profile, all of which may leave essential trace materials behind adversely influencing angiogenesis. Nevertheless, the selection of the best biomaterial and cells still remains an area of hot dispute as such previous studies have not sufficiently classified, integrated, or compared approaches. To address the aforementioned need, this review article summarizes a variety of natural and synthetic scaffolds including hydrogels that support angiogenesis. Furthermore, we review a variety of cell sources utilized for cell seeding and influential factors used for angiogenesis with a concentrated focus on biomechanical factors, with unique stimulatory factors. Lastly, we provide a bottom-to-up overview of angiogenic biomaterials and cell selection, highlighting parameters that need to be addressed in future studies.
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Cell-seeding method seems beneficial in enhancing the biological properties of synthetic matrices.
“Cell-seeding method seems to be beneficial in enhancing the biological properties of the synthetic matrices [222].”
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Hussein, K. H., Park, K.-M., Yu, L., Song, S.-H., Woo, H.-M., & Kwak, H.-H. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2019.12.029 · Cited by 44 · see citing works
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- [1]De Santis MM, Alsafadi HN, Tas S, et al. Extracellular matrix reinforced bioinks for 3D bioprinting human tissue. Adv Mater. 2021; 33: 2005476. Wiley Online Library. doi: 10.1002/adma.202005476 PMC11469085 33300242 · DOI
- [2]Nasr SM, Rabiee N, Hajebi S, et al. Biodegradable nanopolymers in cardiac tissue engineering: from concept towards nanomedicine. Int J Nanomedicine. 2020; 15: 4205. doi: 10.2147/IJN.S245936 32606673 PMC7314574 · DOI
- [3]Matai I, Kaur G, Seyedsalehi A, McClinton A, Laurencin CT. Progress in 3D bioprinting Technology for tissue/organ regenerative engineering. Biomaterials. 2020; 226: 119536. Elsevier. doi: 10.1016/j.biomaterials.2019.119536 31648135 · DOI · Paper page
- [4]Mahfouzi SH, Tali SHS, Amoabediny G. 3D bioprinting for lung and tracheal tissue engineering: criteria, advances, challenges, and future directions. Bioprinting. 2021; 21: e00124. Elsevier. doi: 10.1016/j.bprint.2020.e00124 · DOI
- [5]Shahrezaei F, Mansouri Y, Zinatizadeh A, Akhbari A. Photocatalytic degradation of aniline using TiO2 nanoparticles in a vertical circulating photocatalytic reactor. Int J Photoenergy. 2012; 2012: 1– 8. doi: 10.1155/2012/430638 · DOI
- [6]Ma X, Agas A, Siddiqui Z, et al. Angiogenic peptide hydrogels for treatment of traumatic brain injury. Bioact Mater. 2020; 5(1): 124– 132. doi: 10.1016/j.bioactmat.2020.01.005 32128463 PMC7042674 · DOI
- [7]Rabiee N, Yaraki MT, Garakani SM, et al. Recent advances in porphyrin-based nanocomposites for effective targeted imaging and therapy. Biomaterials. 2020; 232: 119707. doi: 10.1016/j.biomaterials.2019.119707 31874428 PMC7008091 · DOI
- [8]Rahimnejad M, Nasrollahi Boroujeni N, Jahangiri S, et al. Prevascularized micro-/nano-sized spheroid/bead aggregates for vascular tissue engineering. Nano Micro Lett. 2021; 13(1): 1– 24. doi: 10.1007/s40820-021-00697-1 PMC8374027 34409511 · DOI
- [9]Mishra R, Panda AK, De Mandal S, Shakeel M, Bisht SS, Khan J. Natural anti-biofilm agents: strategies to control biofilm-forming pathogens. Front Microbiol. 2020; 11: 2640. Frontiers. doi: 10.3389/fmicb.2020.566325 PMC7658412 33193155 · DOI
- [10]Maghsoudi S, Shahraki BT, Rabiee N, et al. Burgeoning polymer nano blends for improved controlled drug release: a review. Int J Nanomedicine. 2020; 15: 4363. doi: 10.2147/IJN.S252237 32606683 PMC7314622 · DOI
- [11]Tavakolizadeh M, Pourjavadi A, Ansari M, et al. An environmentally friendly wound dressing based on a self-healing, extensible and compressible antibacterial hydrogel. Green Chem. 2021; 23(3): 1312– 1329. doi: 10.1039/D0GC02719G · DOI
- [12]Farokhi M, Mottaghitalab F, Fatahi Y, et al. Silk fibroin scaffolds for common cartilage injuries: possibilities for future clinical applications. Eur Polym J. 2019; 115: 251– 267. Elsevier. doi: 10.1016/j.eurpolymj.2019.03.035 · DOI
- [13]Gupta SK, Dinda AK, Potdar PD, Mishra NC. Modification of decellularized goat-lung scaffold with chitosan/nanohydroxyapatite composite for bone tissue engineering applications. Biomed Res Int. 2013; 2013: 1– 11. Hindawi. doi: 10.1155/2013/651945 PMC3697275 23841083 · DOI
- [14]Vimalraj S, Rajalakshmi S, Saravanan S, et al. Synthesis and characterization of zinc-silibinin complexes: a potential bioactive compound with angiogenic, and antibacterial activity for bone tissue engineering. Colloids Surf B Biointerfaces. 2018; 167: 134– 143. Elsevier. doi: 10.1016/j.colsurfb.2018.04.007 29635136 · DOI
- [15]Chen W, Xu K, Tao B, et al. Multilayered coating of titanium implants promotes coupled osteogenesis and angiogenesis in vitro and in vivo. Acta Biomater. 2018; 74: 489– 504. Elsevier. doi: 10.1016/j.actbio.2018.04.043 29702291 · DOI
- [16]Linville RM, Arevalo D, Maressa JC, Zhao N, Searson PC. Three-dimensional induced pluripotent stem-cell models of human brain angiogenesis. Microvasc Res. 2020; 132: 104042. Elsevier. doi: 10.1016/j.mvr.2020.104042 32673611 PMC7572715 · DOI
- [17]Chakraborty S, Ponrasu T, Chandel S, Dixit M, Muthuvijayan V. Reduced graphene oxide-loaded nanocomposite scaffolds for enhancing angiogenesis in tissue engineering applications. R Soc Open Sci. 2018; 5: 172017. The Royal Society Publishing. doi: 10.1098/rsos.172017 29892387 PMC5990794 · DOI
- [18]Norahan MH, Pourmokhtari M, Saeb MR, Bakhshi B, Zomorrod MS, Baheiraei N. Electroactive cardiac patch containing reduced graphene oxide with potential antibacterial properties. Mater Sci Eng C. 2019; 104: 109921. Elsevier. doi: 10.1016/j.msec.2019.109921 31500009 · DOI
- [19]Wang X, Lin M, Kang Y. Engineering porous -tricalcium phosphate (-TCP) scaffolds with multiple channels to promote cell migration, proliferation, and angiogenesis. ACS Appl Mater Interfaces. 2019; 11: 9223– 9232. ACS Publications. doi: 10.1021/acsami.8b22041 30758175 · DOI
- [20]Hench LL, Splinter RJ, Allen WC, Greenlee TK. Bonding mechanisms at the interface of ceramic prosthetic materials. J Biomed Mater Res. 1971; 5: 117– 141. Wiley Online Library. doi: 10.1002/jbm.820050611 · DOI
- [21]Eke G, Mangir N, Hasirci N, MacNeil S, Hasirci V. Development of a UV crosslinked biodegradable hydrogel containing adipose derived stem cells to promote vascularization for skin wounds and tissue engineering. Biomaterials. 2017; 129: 188– 198. Elsevier. doi: 10.1016/j.biomaterials.2017.03.021 28343005 · DOI
- [22]Wang B, Lv X, Chen S, et al. Use of heparinized bacterial cellulose based scaffold for improving angiogenesis in tissue regeneration. Carbohydr Polym. 2018; 181: 948– 956. Elsevier. doi: 10.1016/j.carbpol.2017.11.055 29254059 · DOI
- [23]Freeman I, Cohen S. The influence of the sequential delivery of angiogenic factors from affinity-binding alginate scaffolds on vascularization. Biomaterials. 2009; 30: 2122– 2131. Elsevier. doi: 10.1016/j.biomaterials.2008.12.057 19152972 · DOI
- [24]Zarrintaj P, Manouchehri S, Ahmadi Z, et al. Agarose-based biomaterials for tissue engineering. Carbohydr Polym. 2018; 187: 66– 84. Elsevier. doi: 10.1016/j.carbpol.2018.01.060 29486846 · DOI
- [25]Rustad KC, Wong VW, Sorkin M, et al. Enhancement of mesenchymal stem cell angiogenic capacity and stemness by a biomimetic hydrogel scaffold. Biomaterials. 2012; 33: 80– 90. Elsevier. doi: 10.1016/j.biomaterials.2011.09.041 21963148 PMC3997302 · DOI
- [26]Laschke MW, Rücker M, Jensen G, et al. Improvement of vascularization of PLGA scaffolds by inosculation of in situ-preformed functional blood vessels with the host microvasculature. Ann Surg. 2008; 248: 939– 948. LWW. doi: 10.1097/SLA.0b013e31818fa52f 19092338 · DOI
- [27]Detsch R, Stoor P, Grünewald A, Roether JA, Lindfors NC, Boccaccini AR. Increase in VEGF secretion from human fibroblast cells by bioactive glass S53P4 to stimulate angiogenesis in bone. J Biomed Mater Res A. 2014; 102: 4055– 4061. Wiley Online Library. doi: 10.1002/jbm.a.35069 24357515 · DOI
- [28]Gniesmer S, Brehm R, Hoffmann A, et al. In vivo analysis of vascularization and biocompatibility of electrospun polycaprolactone fibre mats in the rat femur chamber. J Tissue Eng Regen Med. 2019; 13: 1190– 1202. Wiley Online Library. doi: 10.1002/term.2868 31025510 PMC6771623 · DOI
- [29]Gérard C, Doillon CJ. Facilitating tissue infiltration and angiogenesis in a tubular collagen scaffold. J Biomed Mater Res A. 2010; 93: 615– 624. Wiley Online Library. doi: 10.1002/jbm.a.32568 19591233 · DOI
- [30]Lu J, Guan F, Cui F, et al. Enhanced angiogenesis by the hyaluronic acid hydrogels immobilized with a VEGF mimetic peptide in a traumatic brain injury model in rats. Regen Biomater. 2019; 6: 325– 334. Oxford University Press. doi: 10.1093/rb/rbz027 31827886 PMC6897340 · DOI
- [31]Chan EC, Kuo S-M, Kong AM, et al. Three dimensional collagen scaffold promotes intrinsic vascularisation for tissue engineering applications. PLoS One. 2016; 11: e0149799. Public Library of Science San Francisco, CA USA. doi: 10.1371/journal.pone.0149799 26900837 PMC4762944 · DOI
- [32]Nour S, Baheiraei N, Imani R, et al. A review of accelerated wound healing approaches: biomaterial-assisted tissue remodeling. J Mater Sci Mater Med. 2019; 30(10): 120. doi: 10.1007/s10856-019-6319-6 31630272 · DOI
- [33]Prashanth KVH, Tharanathan RN. Depolymerized products of chitosan as potent inhibitors of tumor-induced angiogenesis. Biochim Biophys Acta Gen Subj. 2005; 1722: 22– 29. Elsevier. doi: 10.1016/j.bbagen.2004.11.009 15716061 · DOI
- [34]Jin H, Pi J, Yang F, et al. Ursolic acid-loaded chitosan nanoparticles induce potent anti-angiogenesis in tumor. Appl Microbiol Biotechnol. 2016; 100: 6643– 6652. Springer. doi: 10.1007/s00253-016-7360-8 26883344 · DOI
- [35]Perets A, Baruch Y, Weisbuch F, Shoshany G, Neufeld G, Cohen S. Enhancing the vascularization of three dimensional porous alginate scaffolds by incorporating controlled release basic fibroblast growth factor microspheres. J Biomed Mater Res A. 2003; 65: 489– 497. Wiley Online Library. doi: 10.1002/jbm.a.10542 12761840 · DOI
- [36]Hegen A, Blois A, Tiron CE, et al. Efficient in vivo vascularization of tissue engineering scaffolds. J Tissue Eng Regen Med. 2011; 5: e52– e62. Wiley Online Library. doi: 10.1002/term.336 20865694 PMC3010488 · DOI
- [37]Singh S, Wu BM, Dunn JCY. Delivery of VEGF using collagen coated polycaprolactone scaffolds stimulates angiogenesis. J Biomed Mater Res A. 2012; 100: 720– 727. Wiley Online Library. doi: 10.1002/jbm.a.34010 22213643 PMC3266436 · DOI
- [38]Kampmann A, Lindhorst D, Schumann P, et al. Additive effect of mesenchymal stem cells and VEGF to vascularization of PLGA scaffolds. Microvasc Res. 2013; 90: 71– 79. Elsevier. doi: 10.1016/j.mvr.2013.07.006 23899416 · DOI
- [39]Dikici S, Claeyssens F, MacNeil S. Bioengineering vascular networks to study angiogenesis and vascularization of physiologically relevant tissue models in vitro. ACS Biomater Sci Eng. 2020; 6: 3513– 3528. ACS Publications. doi: 10.1021/acsbiomaterials.0c00191 32582840 PMC7304666 · DOI
- [40]Gerhardt L-C, Widdows KL, Erol MM, et al. The pro-angiogenic properties of multi-functional bioactive glass composite scaffolds. Biomaterials. 2011; 32: 4096– 4108. Elsevier. doi: 10.1016/j.biomaterials.2011.02.032 21411138 · DOI
- [41]Day RM, Boccaccini AR, Shurey S, et al. Assessment of polyglycolic acid mesh and bioactive glass for soft-tissue engineering scaffolds. Biomaterials. 2004; 25: 5857– 5866. Elsevier. doi: 10.1016/j.biomaterials.2004.01.043 15172498 · DOI
- [42]Zarrintaj P, Ramsey JD, Samadi A, et al. Poloxamer: a versatile tri-block copolymer for biomedical applications. Acta Biomater. 2020; 110: 37– 67. Elsevier. doi: 10.1016/j.actbio.2020.04.028 32417265 · DOI
- [43]Haifei S, Xingang W, Shoucheng W, Zhengwei M, Chuangang Y, Chunmao H. The effect of collagen–chitosan porous scaffold thickness on dermal regeneration in a one-stage grafting procedure. J Mech Behav Biomed Mater. 2014; 29: 114– 125. Elsevier. doi: 10.1016/j.jmbbm.2013.08.031 24076783 · DOI
- [44]Laschke MW, Strohe A, Scheuer C, et al. In vivo biocompatibility and vascularization of biodegradable porous polyurethane scaffolds for tissue engineering. Acta Biomater. 2009; 5: 1991– 2001. Elsevier. doi: 10.1016/j.actbio.2009.02.006 19286433 · DOI
- [45]Bezuidenhout D, Davies N, Black M, Schmidt C, Oosthuysen A, Zilla P. Covalent surface heparinization potentiates porous polyurethane scaffold vascularization. J Biomater Appl. 2010; 24: 401– 418. Sage Publications Sage UK: London, England. doi: 10.1177/0885328208097565 19033329 · DOI
- [46]Lee H-P, Chen P-C, Wang S-W, et al. Plumbagin suppresses endothelial progenitor cell-related angiogenesis in vitro and in vivo. J Funct Foods. 2019; 52: 537– 544. Elsevier. doi: 10.1016/j.jff.2018.11.040 · DOI
- [47]DeLong SA, Moon JJ, West JL. Covalently immobilized gradients of bFGF on hydrogel scaffolds for directed cell migration. Biomaterials. 2005; 26: 3227– 3234. Elsevier. doi: 10.1016/j.biomaterials.2004.09.021 15603817 · DOI
- [48]Zhang K, Song L, Wang J, et al. Strategy for constructing vascularized adipose units in poly (l-glutamic acid) hydrogel porous scaffold through inducing in-situ formation of ASCs spheroids. Acta Biomater. 2017; 51: 246– 257. Elsevier. doi: 10.1016/j.actbio.2017.01.043 28093366 · DOI
- [49]He S, Walimbe T, Chen H, et al. Functionalized extracellular matrix scaffolds loaded with endothelial progenitor cells promote neovascularization and diabetic wound healing. bioRxiv. 2021. Cold Spring Harbor Laboratory. doi: 10.1101/2021.02.02.429469 PMC8636679 34901560 · DOI
- [50]Fishman JM, Wiles K, Lowdell MW, et al. Airway tissue engineering: an update. Expert Opin Biol Ther. 2014; 14: 1477– 1491. Taylor & Francis. doi: 10.1517/14712598.2014.938631 25102044 · DOI
- [51]Yazdi MK, Taghizadeh A, Taghizadeh M, et al. Agarose-based biomaterials for advanced drug delivery. J Control Release. 2020; 326: 523– 543. 32702391
- [52]Verstegen MMA, Willemse J, Van Den Hoek S, et al. Decellularization of whole human liver grafts using controlled perfusion for transplantable organ bioscaffolds. Stem Cells Dev. 2017; 26: 1304– 1315. Mary Ann Liebert, Inc. 140 Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA. doi: 10.1089/scd.2017.0095 28665233 · DOI
- [53]Hajebi S, Mohammadi Nasr S, Rabiee N, et al. Bioresorbable composite polymeric materials for tissue engineering applications. Int J Polym Mater Polym Biomater. 2021; 1– 15. doi: 10.1080/00914037.2020.1765365 · DOI
- [54]Baheiraei N, Eyni H, Bakhshi B, Najafloo R, Rabiee N. Effects of strontium ions with potential antibacterial activity on in vivo bone regeneration. Sci Rep. 2021; 11(1): 1– 9. doi: 10.1038/s41598-021-88058-1 33888790 PMC8062523 · DOI
- [55]Zhou H, Kitano K, Ren X, et al. Bioengineering human lung grafts on porcine matrix. Ann Surg. 2018; 267: 590– 598. LWW. doi: 10.1097/SLA.0000000000002129 28085694 · DOI
- [56]Rabiee N, Bagherzadeh M, Ghadiri AM, et al. Multifunctional 3D hierarchical bioactive green carbon-based nanocomposites. ACS Sustain Chem Eng. 2021; 9(26): 8706– 8720. doi: 10.1021/acssuschemeng.1c00781 · DOI
- [57]Rabiee N, Bagherzadeh M, Heidarian Haris M, et al. Polymer-coated NH2-UiO-66 for the codelivery of DOX/pCRISPR. ACS Appl Mater Interfaces. 2021; 13(9): 10796– 10811. doi: 10.1021/acsami.1c01460 33621063 · DOI
- [58]Nichols JE, La Francesca S, Vega SP, et al. Giving new life to old lungs: methods to produce and assess whole human paediatric bioengineered lungs. J Tissue Eng Regen Med. 2017; 11: 2136– 2152. Wiley Online Library. doi: 10.1002/term.2113 26756722 · DOI
- [59]Rabiee N, Bagherzadeh M, Jouyandeh M, et al. Natural polymers decorated MOF-MXene nanocarriers for co-delivery of doxorubicin/pCRISPR. ACS Applied Bio Mater. 2021; 4(6): 5106– 5121. doi: 10.1021/acsabm.1c00332 35007059 · DOI
- [60]Gilpin SE, Charest JM, Ren X, et al. Regenerative potential of human airway stem cells in lung epithelial engineering. Biomaterials. 2016; 108: 111– 119. Elsevier. doi: 10.1016/j.biomaterials.2016.08.055 27622532 PMC5035637 · DOI
- [61]Saberianpour S, Heidarzadeh M, Geranmayeh MH, Hosseinkhani H, Rahbarghazi R, Nouri M. Tissue engineering strategies for the induction of angiogenesis using biomaterials. J Biol Eng. 2018; 12: 1– 15. Springer. doi: 10.1186/s13036-018-0133-4 30603044 PMC6307144 · DOI
- [62]El-Sherbiny IM, Yacoub MH. Hydrogel scaffolds for tissue engineering: progress and challenges. Glob Cardiol Sci Pract. 2013; 2013: 38. Hamad bin Khalifa University Press (HBKU Press). doi: 10.5339/gcsp.2013.38 PMC3963751 24689032 · DOI
- [63]Tsuchiya T, Obata T, Hatachi G, Nagayasu T. Lung microvascular niche, repair, and engineering. Front Bioeng Biotechnol. 2020; 8: 105. Frontiers. doi: 10.3389/fbioe.2020.00105 32154234 PMC7047880 · DOI
- [64]Bourke BM, Roche WR, Appleberg M. Endothelial cell harvest for seeding vascular prostheses: the influence of technique on cell function, viability, and number. J Vasc Surg. 1986; 4: 257– 263. Elsevier. doi: 10.1016/0741-5214(86)90195-3 3528533 · DOI · Paper page
- [65]Rücker M, Laschke MW, Junker D, et al. Angiogenic and inflammatory response to biodegradable scaffolds in dorsal skinfold chambers of mice. Biomaterials. 2006; 27: 5027– 5038. Elsevier. doi: 10.1016/j.biomaterials.2006.05.033 16769111 · DOI
- [66]Druecke D, Langer S, Lamme E, et al. Neovascularization of poly (ether ester) block copolymer scaffolds in vivo: long term investigations using intravital fluorescent microscopy. J Biomed Mater Res A. 2004; 68: 10– 18. Wiley Online Library. doi: 10.1002/jbm.a.20016 14661244 · DOI
- [67]Nillesen STM, Geutjes PJ, Wismans R, Schalkwijk J, Daamen WF, van Kuppevelt TH. Increased angiogenesis and blood vessel maturation in acellular collagen–heparin scaffolds containing both FGF2 and VEGF. Biomaterials. 2007; 28: 1123– 1131. Elsevier. doi: 10.1016/j.biomaterials.2006.10.029 17113636 · DOI
- [68]Laschke MW, Rücker M, Jensen G, et al. Incorporation of growth factor containing Matrigel promotes vascularization of porous PLGA scaffolds. J Biomed Mater Res A. 2008; 85: 397– 407. Wiley Online Library. doi: 10.1002/jbm.a.31503 17688245 · DOI
- [69]Shepherd BR, Enis DR, Wang F, et al. Vascularization and engraftment of a human skin substitute using circulating progenitor cell derived endothelial cells. FASEB J. 2006; 20: 1739– 1741. Wiley Online Library. doi: 10.1096/fj.05-5682fje 16807367 · DOI
- [70]Rabiee N, Bagherzadeh M, Ghadiri AM, et al. Turning toxic nanomaterials into a safe and bioactive nanocarrier for co-delivery of DOX/pCRISPR. ACS Applied Bio Mater. 2021; 4(6): 5336– 5351. ACS Publications. doi: 10.1021/acsabm.1c00447 35007014 · DOI
- [71]Wagner ER, Parry J, Dadsetan M, et al. VEGF-mediated angiogenesis and vascularization of a fumarate-crosslinked polycaprolactone (PCLF) scaffold. Connect Tissue Res. 2018; 59: 542– 549. Taylor & Francis. doi: 10.1080/03008207.2018.1424145 29513041 · DOI
- [72]Seidi F, Yazdi MK, Jouyandeh M, et al. Chitosan-based blends for biomedical applications. Int J Biol Macromol. 2021; 183: 1818– 1850. Elsevier. 33971230
- [73]Manouchehri S, Bagheri B, Rad SH, et al. Electroactive bio-epoxy incorporated chitosan-oligoaniline as an advanced hydrogel coating for neural interfaces. Prog Org Coat. 2019; 131: 389– 396. Elsevier. doi: 10.1016/j.porgcoat.2019.03.022 · DOI
- [74]Chen M, Zhang Y, Zhang W, Li J. Polyhedral oligomeric silsesquioxane-incorporated gelatin hydrogel promotes angiogenesis during vascularized bone regeneration. ACS Appl Mater Interfaces. 2020; 12(20): 22410– 22425. doi: 10.1021/acsami.0c00714 32349479 · DOI
- [75]Long G, Liu D, He X, et al. A dual functional collagen scaffold coordinates angiogenesis and inflammation for diabetic wound healing. Biomater Sci. 2020; 8: 6337– 6349. Royal Society of Chemistry. doi: 10.1039/D0BM00999G 33025970 · DOI
- [76]Wong HK, Lam CRI, Wen F, et al. Novel method to improve vascularization of tissue engineered constructs with biodegradable fibers. Biofabrication. 2016; 8: 15004. IOP Publishing. doi: 10.1088/1758-5090/8/1/015004 26741237 · DOI
- [77]He Q, Zhao Y, Chen B, et al. Improved cellularization and angiogenesis using collagen scaffolds chemically conjugated with vascular endothelial growth factor. Acta Biomater. 2011; 7: 1084– 1093. Elsevier. doi: 10.1016/j.actbio.2010.10.022 20977949 · DOI
- [78]Andrade CF, Wong AP, Waddell TK, Keshavjee S, Liu M. Cell-based tissue engineering for lung regeneration. Am J Physiol Lung Cell Mol Physiol. 2007; 292: L510– L518. American Physiological Society. doi: 10.1152/ajplung.00175.2006 17028264 · DOI
- [79]Liu S, Zhang H, Zhang X, et al. Synergistic angiogenesis promoting effects of extracellular matrix scaffolds and adipose-derived stem cells during wound repair. Tissue Eng Part A. 2011; 17: 725– 739. Mary Ann Liebert, Inc. 140 Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA. doi: 10.1089/ten.tea.2010.0331 20929282 · DOI
- [80]Hsia CCW, Hyde DM, Weibel ER. Lung structure and the intrinsic challenges of gas exchange. Compr Physiol. 2016; 6: 827. NIH Public Access. 27065169 PMC5026132
- [81]Kargozar S, Baino F, Hamzehlou S, Hill RG, Mozafari M. Bioactive glasses: sprouting angiogenesis in tissue engineering. Trends Biotechnol. 2018; 36: 430– 444. Elsevier. doi: 10.1016/j.tibtech.2017.12.003 29397989 · DOI
- [82]Gerhardt LC, Widdows KL, Erol MM, et al. Neocellularization and neovascularization of nanosized bioactive glass coated decellularized trabecular bone scaffolds. J Biomed Mater Res A. 2013; 101: 827– 841. Wiley Online Library. doi: 10.1002/jbm.a.34373 22968899 · DOI
- [83]Shie M-Y, Ding S-J, Chang H-C. The role of silicon in osteoblast-like cell proliferation and apoptosis. Acta Biomater. 2011; 7: 2604– 2614. Elsevier. doi: 10.1016/j.actbio.2011.02.023 21345382 · DOI
- [84]Walker D, Wood S, Southgate J, Holcombe M, Smallwood R. An integrated agent-mathematical model of the effect of intercellular signalling via the epidermal growth factor receptor on cell proliferation. J Theor Biol. 2006; 242: 774– 789. Elsevier. doi: 10.1016/j.jtbi.2006.04.020 16765384 · DOI
- [85]Boyacioglu SO, Korkmaz M, Kahraman E, Yildirim H, Bora S, Ataman OY. Biological effects of tolerable level chronic boron intake on transcription factors. J Trace Elem Med Biol. 2017; 39: 30– 35. Elsevier. doi: 10.1016/j.jtemb.2016.06.009 27908420 · DOI
- [86]Li J, Zhai D, Lv F, et al. Preparation of copper-containing bioactive glass/eggshell membrane nanocomposites for improving angiogenesis, antibacterial activity and wound healing. Acta Biomater. 2016; 36: 254– 266. Elsevier. doi: 10.1016/j.actbio.2016.03.011 26965395 · DOI
- [87]Milan PB, Khamseh S, Zarrintaj P, et al. Copper-enriched diamond-like carbon coatings promote regeneration at the bone–implant interface. Heliyon. 2020; 6: e03798. Elsevier. 32368647 PMC7184533
- [88]Stoor P, Frantzen J. Influence of bioactive glass S53P4 granules and putty on osteomyelitis associated bacteria in vitro. Biomed Glas. 2017; 3: 79– 85. De Gruyter Open. doi: 10.1515/bglass-2017-0007 · DOI
- [89]Zhang D, Leppäranta O, Munukka E, et al. Antibacterial effects and dissolution behavior of six bioactive glasses. J Biomed Mater Res A. 2010; 93: 475– 483. Wiley Online Library. doi: 10.1002/jbm.a.32564 19582832 · DOI
- [90]Kim -J-J, El-Fiqi A, Kim H-W. Synergetic cues of bioactive nanoparticles and nanofibrous structure in bone scaffolds to stimulate osteogenesis and angiogenesis. ACS Appl Mater Interfaces. 2017; 9(3): 2059– 2073. doi: 10.1021/acsami.6b12089 28029246 · DOI
- [91]Zarrintaj P, Mahmodi G, Manouchehri S, et al. Zeolite in tissue engineering: opportunities and challenges. MedComm. 2020; 1: 5– 34. Wiley Online Library. doi: 10.1002/mco2.5 34766107 PMC8489670 · DOI
- [92]Liakouli V, Cipriani P, Di Benedetto P, et al. The role of extracellular matrix components in angiogenesis and fibrosis: possible implication for systemic sclerosis. Mod Rheumatol. 2018; 28(6): 922– 932. doi: 10.1080/14397595.2018.1431004 29351724 · DOI
- [93]Zhang J, Liu X, Ma K, et al. Collagen/heparin scaffold combined with vascular endothelial growth factor promotes the repair of neurological function in rats with traumatic brain injury. Biomater Sci. 2021; 9(3): 745– 764. doi: 10.1039/C9BM01446B 33200759 · DOI
- [94]Zhang B, Radisic M. Organ-Level Vascularization: The Mars Mission of Bioengineering. Elsevier; 2020. 31668537
- [95]Liu K, Chen C, Zhang H, Chen Y, Zhou S. Adipose stem cell derived exosomes in combination with hyaluronic acid accelerate wound healing through enhancing re epithelialization and vascularization. Br J Dermatol. 2019; 181: 854– 856. doi: 10.1111/bjd.17984 30953591 · DOI
- [96]Bahramsoltani M, Slosarek I, De Spiegelaere W, Plendl J. Angiogenesis and collagen type IV expression in different endothelial cell culture systems. Anat Histol Embryol. 2014; 43(2): 103– 115. Wiley Online Library. doi: 10.1111/ahe.12052 23551189 · DOI
- [97]Ehterami A, Salehi M, Farzamfar S, et al. A promising wound dressing based on alginate hydrogels containing vitamin D3 cross-linked by calcium carbonate/d-glucono- -lactone. Biomed Eng Lett. 2020; 10: 309. Springer. doi: 10.1007/s13534-020-00155-8 32431957 PMC7235134 · DOI
- [98]Mohebbi S, Nezhad MN, Zarrintaj P, et al. Chitosan in biomedical engineering: a critical review. Curr Stem Cell Res Ther. 2019; 14: 93– 116. Bentham Science Publishers. 30207244
- [99]Zhang W, Chen L, Chen J, et al. Silk fibroin biomaterial shows safe and effective wound healing in animal models and a randomized controlled clinical trial. Adv Healthcare Mater. 2017; 6(10): 1700121. doi: 10.1002/adhm.201700121 28337854 · DOI
- [100]Ribatti D, Nico B, Crivellato E. The role of pericytes in angiogenesis. Int J Dev Biol. 2011; 55(3): 261– 268. doi: 10.1387/ijdb.103167dr 21710434 · DOI
- [101]Morgan JP, Delnero PF, Zheng Y, et al. Formation of microvascular networks in vitro. Nat Protoc. 2013; 8: 1820– 1836. Nature Publishing Group. doi: 10.1038/nprot.2013.110 23989676 · DOI
- [102]Wang B, Lv X, Li Z, et al. Urethra-inspired biomimetic scaffold: a therapeutic strategy to promote angiogenesis for urethral regeneration in a rabbit model. Acta Biomater. 2020; 102: 247– 258. Elsevier. doi: 10.1016/j.actbio.2019.11.026 31734410 · DOI
- [103]Sweeney SM, DiLullo G, Slater SJ, et al. Angiogenesis in collagen I requires 2 1 ligation of a GFP* GER sequence and possibly p38 MAPK activation and focal adhesion disassembly. J Biol Chem. 2003; 278: 30516– 30524. ASBMB. doi: 10.1074/jbc.M304237200 12788934 · DOI
- [104]Schechner JS, Nath AK, Zheng L, et al. In vivo formation of complex microvessels lined by human endothelial cells in an immunodeficient mouse. Proc Natl Acad Sci. 2000; 97: 9191– 9196. National Acad Sciences. doi: 10.1073/pnas.150242297 10890921 PMC16844 · DOI
- [105]Zhang S, Chen J, Yu Y, Dai K, Wang J, Liu C. Accelerated bone regenerative efficiency by regulating sequential release of BMP-2 and VEGF and synergism with sulfated chitosan. ACS Biomater Sci Eng. 2019; 5(4): 1944– 1955. doi: 10.1021/acsbiomaterials.8b01490 33405523 · DOI
- [106]Campbell KT, Stilhano RS, Silva EA. Enzymatically degradable alginate hydrogel systems to deliver endothelial progenitor cells for potential revasculature applications. Biomaterials. 2018; 179: 109– 121. Elsevier. doi: 10.1016/j.biomaterials.2018.06.038 29980073 PMC6746553 · DOI
- [107]Mony MP, Shenoy SJ, Raj R, et al. Gelatin-modified cholecyst-derived Scaffold promotes angiogenesis and faster healing of diabetic wounds. ACS Applied Bio Mater. 2021; 4(4): 3320– 3331. doi: 10.1021/acsabm.0c01648 35014418 · DOI
- [108]Anderson SM, Siegman SN, Segura T. The effect of vascular endothelial growth factor (VEGF) presentation within fibrin matrices on endothelial cell branching. Biomaterials. 2011; 32: 7432– 7443. Elsevier. doi: 10.1016/j.biomaterials.2011.06.027 21783250 PMC3601829 · DOI
- [109]Shi X, Zhou K, Huang F, Wang C. Interaction of hydroxyapatite nanoparticles with endothelial cells: internalization and inhibition of angiogenesis in vitro through the PI3K/Akt pathway. Int J Nanomedicine. 2017; 12: 5781. Dove Press. doi: 10.2147/IJN.S140179 28848353 PMC5557617 · DOI
- [110]Aljohi A, Matou-Nasri S, Liu D, Al-Khafaji N, Slevin M, Ahmed N. Momordica charantia extracts protect against inhibition of endothelial angiogenesis by advanced glycation endproducts in vitro. Food Funct. 2018; 9: 5728– 5739. Royal Society of Chemistry. doi: 10.1039/C8FO00297E 30318521 · DOI
- [111]Dohle E, El Bagdadi K, Sader R, Choukroun J, James Kirkpatrick C, Ghanaati S. Platelet rich fibrin based matrices to improve angiogenesis in an in vitro co culture model for bone tissue engineering. J Tissue Eng Regen Med. 2018; 12: 598– 610. Wiley Online Library. doi: 10.1002/term.2475 28509340 PMC5888144 · DOI
- [112]Uwamori H, Higuchi T, Arai K, Sudo R. Integration of neurogenesis and angiogenesis models for constructing a neurovascular tissue. Sci Rep. 2017; 7: 1– 11. Nature Publishing Group. doi: 10.1038/s41598-017-17411-0 29229920 PMC5725567 · DOI
- [113]Naderi H, Matin MM, Bahrami AR. Critical issues in tissue engineering: biomaterials, cell sources, angiogenesis, and drug delivery systems. J Biomater Appl. 2011; 26: 383– 417. Sage Publications Sage UK: London, England. doi: 10.1177/0885328211408946 21926148 · DOI
- [114]Mondrinos MJ, Koutzaki SH, Poblete HM, Crisanti MC, Lelkes PI, Finck CM. In vivo pulmonary tissue engineering: contribution of donor-derived endothelial cells to construct vascularization. Tissue Eng Part A. 2008; 14: 361– 368. Mary Ann Liebert, Inc. 140 Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA. doi: 10.1089/tea.2007.0041 18333788 · DOI
- [115]Liu S, Yu J, Zhang Q, et al. Dual cross-linked HHA hydrogel supplies and regulates MΦ2 for synergistic improvement of immunocompromise and impaired angiogenesis to enhance diabetic chronic wound healing. Biomacromolecules. 2020; 21(9): 3795– 3806. doi: 10.1021/acs.biomac.0c00891 32786521 · DOI
- [116]Grigoryan B, Paulsen SJ, Corbett DC, et al. Multivascular networks and functional intravascular topologies within biocompatible hydrogels. Science. 2019; 364: 458– 464. American Association for the Advancement of Science. doi: 10.1126/science.aav9750 31048486 PMC7769170 · DOI
- [117]Van Hove AH, Burke K, Antonienko E, Brown E III, Benoit DSW. Enzymatically-responsive pro-angiogenic peptide-releasing poly (ethylene glycol) hydrogels promote vascularization in vivo. J Control Release. 2015; 217: 191– 201. Elsevier. doi: 10.1016/j.jconrel.2015.09.005 26365781 PMC4626208 · DOI
- [118]Mokhames Z, Rezaie Z, Ardeshirylajimi A, Basiri A, Taheri M, Omrani MD. VEGF-incorporated PVDF/collagen nanofibrous scaffold for bladder wall regeneration and angiogenesis. Int J Polym Mater Polym Biomater. 2021; 70: 521– 529. Taylor & Francis. doi: 10.1080/00914037.2020.1740985 · DOI
- [119]Gao W, Jin W, Li Y, et al. A highly bioactive bone extracellular matrix-biomimetic nanofibrous system with rapid angiogenesis promotes diabetic wound healing. J Mater Chem B. 2017; 5: 7285– 7296. Royal Society of Chemistry. doi: 10.1039/C7TB01484H 32264178 · DOI
- [120]Abebayehu D, Spence AJ, McClure MJ, Haque TT, Rivera KO, Ryan JJ. Polymer scaffold architecture is a key determinant in mast cell inflammatory and angiogenic responses. J Biomed Mater Res A. 2019; 107: 884– 892. Wiley Online Library. doi: 10.1002/jbm.a.36605 30615257 PMC6551205 · DOI
- [121]Gugutkov D, Gustavsson J, Cantini M, Salmeron sánchez M, Altankov G. Electrospun fibrinogen–PLA nanofibres for vascular tissue engineering. J Tissue Eng Regen Med. 2017; 11: 2774– 2784. Wiley Online Library. doi: 10.1002/term.2172 27238477 · DOI
- [122]Klumpp D, Rudisile M, Kühnle RI, et al. Three dimensional vascularization of electrospun PCL/collagen blend nanofibrous scaffolds in vivo. J Biomed Mater Res A. 2012; 100: 2302– 2311. Wiley Online Library. doi: 10.1002/jbm.a.34172 22508579 · DOI
- [123]Nazarnezhad S, Baino F, Kim H-W, Webster TJ, Kargozar S. Electrospun nanofibers for improved angiogenesis: promises for tissue engineering applications. Nanomaterials. 2020; 10: 1609. Multidisciplinary Digital Publishing Institute. doi: 10.3390/nano10081609 PMC7466668 32824491 · DOI
- [124]Cui L, Liang J, Liu H, Zhang K, Li J. Nanomaterials for angiogenesis in skin tissue engineering. Tissue Eng Part B Rev. 2020; 26(3): 203– 216. doi: 10.1089/ten.teb.2019.0337 31964266 · DOI
- [125]Levenberg S, Rouwkema J, Macdonald M, et al. Engineering vascularized skeletal muscle tissue. Nat Biotechnol. 2005; 23: 879– 884. Nature Publishing Group. doi: 10.1038/nbt1109 15965465 · DOI
- [126]Thevenot PT, Nair AM, Shen J, Lotfi P, Ko C-Y, Tang L. The effect of incorporation of SDF-1 into PLGA scaffolds on stem cell recruitment and the inflammatory response. Biomaterials. 2010; 31: 3997– 4008. Elsevier. doi: 10.1016/j.biomaterials.2010.01.144 20185171 PMC2838969 · DOI
- [127]Hoenig MR, Bianchi C, Sellke FW. Hypoxia inducible factor-1, endothelial progenitor cells, monocytes, cardiovascular risk, wound healing, cobalt and hydralazine: a unifying hypothesis. Curr Drug Targets. 2008; 9: 422– 435. Bentham Science Publishers. doi: 10.2174/138945008784221215 18473772 · DOI
- [128]Dong D, Li J, Cui M, et al. In situ “clickable” zwitterionic starch-based hydrogel for 3D cell encapsulation. ACS Appl Mater Interfaces. 2016; 8(7): 4442– 4455. doi: 10.1021/acsami.5b12141 26817499 · DOI
- [129]Tremblay PL, Hudon V, Berthod F, Germain L, Auger FA. Inosculation of tissue engineered capillaries with the host’s vasculature in a reconstructed skin transplanted on mice. Am J Transpl. 2005; 5: 1002– 1010. Wiley Online Library. doi: 10.1111/j.1600-6143.2005.00790.x 15816880 · DOI
- [130]Zarrintaj P, Zangene E, Manouchehri S, et al. Conductive biomaterials as nerve conduits: recent advances and future challenges. Appl Mater Today. 2020; 20: 100784. Elsevier. doi: 10.1016/j.apmt.2020.100784 · DOI
- [131]Kito T, Shibata R, Ishii M, et al. iPS cell sheets created by a novel magnetite tissue engineering method for reparative angiogenesis. Sci Rep. 2013; 3: 1– 8. Nature Publishing Group. doi: 10.1038/srep01418 PMC3593218 23475393 · DOI
- [132]Divakar P, Caruso I, Moodie KL, Theiler RN, Hoopes PJ, Wegst UGK. Design, manufacture, and in vivo testing of a tissue scaffold for permanent female sterilization by tubal occlusion. MRS Adv. 2018; 3: 1685– 1690. Materials Research Society. doi: 10.1557/adv.2018.57 30416761 PMC6223265 · DOI
- [133]Gorustovich AA, Roether JA, Boccaccini AR. Effect of bioactive glasses on angiogenesis: a review of in vitro and in vivo evidences. Tissue Eng Part B Rev. 2010; 16: 199– 207. Mary Ann Liebert, Inc. 140 Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA. doi: 10.1089/ten.teb.2009.0416 19831556 · DOI
- [134]Maghsoudlou P, Georgiades F, Tyraskis A, et al. Preservation of micro-architecture and angiogenic potential in a pulmonary acellular matrix obtained using intermittent intra-tracheal flow of detergent enzymatic treatment. Biomaterials. 2013; 34: 6638– 6648. Elsevier. doi: 10.1016/j.biomaterials.2013.05.015 23727263 PMC3988964 · DOI
- [136]Merckx G, Tay H, Lo Monaco M, et al. Chorioallantoic membrane assay as model for angiogenesis in tissue engineering: focus on stem cells. Tissue Eng Part B Rev. 2020; 26: 519– 539. Mary Ann Liebert, Inc. publishers 140 Huguenot Street, 3rd Floor New. doi: 10.1089/ten.teb.2020.0048 32220219 · DOI
- [137]Gilpin SE, Wagner DE. Acellular human lung scaffolds to model lung disease and tissue regeneration. Eur Respir Rev. 2018; 27: 180021. Eur Respiratory Soc. doi: 10.1183/16000617.0021-2018 29875137 PMC9488127 · DOI
- [138]Kato Y, Iwata T, Morikawa S, Yamato M, Okano T, Uchigata Y. Allogeneic transplantation of an adipose-derived stem cell sheet combined with artificial skin accelerates wound healing in a rat wound model of type 2 diabetes and obesity. Diabetes. 2015; 64: 2723– 2734. Am Diabetes Assoc. doi: 10.2337/db14-1133 25795216 · DOI
- [139]Auger FA, Gibot L, Lacroix D. The pivotal role of vascularization in tissue engineering. Annu Rev Biomed Eng. 2013; 15: 177– 200. Annual Reviews. doi: 10.1146/annurev-bioeng-071812-152428 23642245 · DOI
- [140]Chen L, Xing Q, Zhai Q, et al. Pre-vascularization enhances therapeutic effects of human mesenchymal stem cell sheets in full thickness skin wound repair. Theranostics. 2017; 7: 117. Ivyspring International Publisher. doi: 10.7150/thno.17031 28042321 PMC5196890 · DOI
- [141]Dickman CTD, Russo V, Thain K, et al. Functional characterization of 3D contractile smooth muscle tissues generated using a unique microfluidic 3D bioprinting Technology. FASEB J. 2020; 34: 1652– 1664. Wiley Online Library. doi: 10.1096/fj.201901063RR 31914670 · DOI
- [142]Ren X, Moser PT, Gilpin SE, et al. Engineering pulmonary vasculature in decellularized rat and human lungs. Nat Biotechnol. 2015; 33: 1097– 1102. Nature Publishing Group. doi: 10.1038/nbt.3354 26368048 · DOI
- [143]Zarrintaj P, Moghaddam AS, Manouchehri S, et al. Can regenerative medicine and nanotechnology combine to heal wounds? The search for the ideal wound dressing. Nanomedicine. 2017; 12: 2403– 2422. Future Medicine. doi: 10.2217/nnm-2017-0173 28868968 · DOI
- [144]Nilforoushzadeh MA, Khodadadi Yazdi M, Baradaran Ghavami S, et al. Mesenchymal stem cell spheroids embedded in an injectable thermosensitive hydrogel: an in situ drug formation platform for accelerated wound healing. ACS Biomater Sci Eng. 2020; 6: 5096– 5109. ACS Publications. doi: 10.1021/acsbiomaterials.0c00988 33455261 · DOI
- [145]Li T, Ma H, Ma H, et al. Mussel-inspired nanostructures potentiate the immunomodulatory properties and angiogenesis of mesenchymal stem cells. ACS Appl Mater Interfaces. 2019; 11(19): 17134– 17146. doi: 10.1021/acsami.8b22017 31008578 · DOI
- [146]White AC, Lavine KJ, Ornitz DM. FGF9 and SHH Regulate Mesenchymal Vegfa Expression and Development of the Pulmonary Capillary Network. Oxford University Press for The Company of Biologists Limited; 2007. PMC2099314 17881491
- [147]Genova T, Petrillo S, Zicola E, et al. The crosstalk between osteodifferentiating stem cells and endothelial cells promotes angiogenesis and bone formation. Front Physiol. 2019; 10: 1291. Frontiers. doi: 10.3389/fphys.2019.01291 31681005 PMC6802576 · DOI
- [148]McFadden TM, Duffy GP, Allen AB, et al. The delayed addition of human mesenchymal stem cells to pre-formed endothelial cell networks results in functional vascularization of a collagen–glycosaminoglycan scaffold in vivo. Acta Biomater. 2013; 9: 9303– 9316. Elsevier. doi: 10.1016/j.actbio.2013.08.014 23958783 · DOI
- [149]Mura M, Binnie M, Han B, et al. Functions of type II pneumocyte-derived vascular endothelial growth factor in alveolar structure, acute inflammation, and vascular permeability. Am J Pathol. 2010; 176: 1725– 1734. Elsevier. doi: 10.2353/ajpath.2010.090209 20167862 PMC2843464 · DOI
- [150]Panina YA, Yakimov AS, Komleva YK, et al. Plasticity of adipose tissue-derived stem cells and regulation of angiogenesis. Front Physiol. 2018; 9: 1656. Frontiers. doi: 10.3389/fphys.2018.01656 30534080 PMC6275221 · DOI
- [151]Ling T-Y, Liu Y-L, Huang Y-K, et al. Differentiation of lung stem/progenitor cells into alveolar pneumocytes and induction of angiogenesis within a 3D gelatin–microbubble scaffold. Biomaterials. 2014; 35: 5660– 5669. Elsevier. doi: 10.1016/j.biomaterials.2014.03.074 24746968 · DOI
- [152]Spiller KL, Anfang RR, Spiller KJ, et al. The role of macrophage phenotype in vascularization of tissue engineering scaffolds. Biomaterials. 2014; 35(15): 4477– 4488. doi: 10.1016/j.biomaterials.2014.02.012 24589361 PMC4000280 · DOI · Paper page
- [153]Danese S, Dejana E, Fiocchi C. Immune regulation by microvascular endothelial cells: directing innate and adaptive immunity, coagulation, and inflammation. J Immunol. 2007; 178: 6017– 6022. Am Assoc Immnol. doi: 10.4049/jimmunol.178.10.6017 17475823 · DOI
- [154]Noonan DM, Barbaro ADL, Vannini N, Mortara L, Albini A. Inflammation, inflammatory cells and angiogenesis: decisions and indecisions. Cancer Metastasis Rev. 2008; 27: 31– 40. Springer. doi: 10.1007/s10555-007-9108-5 18087678 · DOI
- [155]Wagner EM, Sánchez J, McClintock JY, Jenkins J, Moldobaeva A. Inflammation and ischemia-induced lung angiogenesis. Am J Physiol Lung Cell Mol Physiol. 2008; 294: L351– L357. American Physiological Society. doi: 10.1152/ajplung.00369.2007 18156440 · DOI
- [156]Laschke MW, Menger MD. Spheroids as vascularization units: from angiogenesis research to tissue engineering applications. Biotechnol Adv. 2017; 35: 782– 791. Elsevier. doi: 10.1016/j.biotechadv.2017.07.002 28694177 · DOI
- [157]Zimmermann JA, Mcdevitt TC. Pre-conditioning mesenchymal stromal cell spheroids for immunomodulatory paracrine factor secretion. Cytotherapy. 2014; 16(3): 331– 345. doi: 10.1016/j.jcyt.2013.09.004 24219905 · DOI
- [158]Lee E, Takahashi H, Pauty J, et al. A 3D in vitro pericyte-supported microvessel model: visualisation and quantitative characterisation of multistep angiogenesis. J Mater Chem B. 2018; 6: 1085– 1094. Royal Society of Chemistry. doi: 10.1039/C7TB03239K 32254296 · DOI
- [159]Grönman M, Moisio O, Li X-G, et al. Association between [68Ga] NODAGA-RGDyK uptake and dynamics of angiogenesis in a human cell-based 3D model. Mol Biol Rep. 2021; 48(6): 5347– 5353. Springer. 34213709 PMC8318966
- [160]Komaki M, Numata Y, Morioka C, et al. Exosomes of human placenta-derived mesenchymal stem cells stimulate angiogenesis. Stem Cell Res Ther. 2017; 8: 1– 12. BioMed Central. doi: 10.1186/s13287-017-0660-9 28974256 PMC5627451 · DOI
- [161]Heise RL, Stober V, Cheluvaraju C, Hollingsworth JW, Garantziotis S. Mechanical stretch induces epithelial-mesenchymal transition in alveolar epithelia via hyaluronan activation of innate immunity. J Biol Chem. 2011; 286: 17435– 17444. ASBMB. doi: 10.1074/jbc.M110.137273 21398522 PMC3093817 · DOI
- [162]Milkiewicz M, Doyle JL, Fudalewski T, Ispanovic E, Aghasi M, Haas TL. HIF 1 and HIF 2 play a central role in stretch induced but not shear stress induced angiogenesis in rat skeletal muscle. J Physiol. 2007; 583: 753– 766. Wiley Online Library. doi: 10.1113/jphysiol.2007.136325 17627993 PMC2277012 · DOI
- [163]Ohata K, Ott HC. Human-scale lung regeneration based on decellularized matrix scaffolds as a biologic platform. Surg Today. 2020; 50: 633– 643. Springer. doi: 10.1007/s00595-020-02000-y 32363425 PMC7305261 · DOI
- [164]Varley C, Hill G, Pellegrin S, et al. Autocrine regulation of human urothelial cell proliferation and migration during regenerative responses in vitro. Exp Cell Res. 2005; 306: 216– 229. Elsevier. doi: 10.1016/j.yexcr.2005.02.004 15878346 · DOI
- [165]Nossa R, Costa J, Cacopardo L, Ahluwalia A. Breathing in vitro: designs and applications of engineered lung models. J Tissue Eng. 2021; 12: 20417314211008696. doi: 10.1177/20417314211008696 33996022 PMC8107677 · DOI
- [166]Fuchs S, Motta A, Migliaresi C, Kirkpatrick CJ. Outgrowth endothelial cells isolated and expanded from human peripheral blood progenitor cells as a potential source of autologous cells for endothelialization of silk fibroin biomaterials. Biomaterials. 2006; 27(31): 5399– 5408. doi: 10.1016/j.biomaterials.2006.06.015 16837042 · DOI
- [167]Bruzauskaite I, Raudoniute J, Denkovskij J, et al. Native matrix-based human lung alveolar tissue model in vitro: studies of the reparatory actions of mesenchymal stem cells. Cytotechnology. 2017; 69(1): 1– 17. doi: 10.1007/s10616-016-0021-z 27905026 PMC5264619 · DOI
- [168]Ma J, Both SK, Yang F, et al. Concise review: cell‐based strategies in bone tissue engineering and regenerative medicine. Stem Cells Transl Med. 2014; 3(1): 98– 107. doi: 10.5966/sctm.2013-0126 24300556 PMC3902295 · DOI
- [169]Iravani S, Varma RS. Green synthesis, biomedical and biotechnological applications of carbon and graphene quantum dots. A review. Environ Chem Lett. 2020; 1– 25. doi: 10.1007/s10311-020-00984-0 PMC7088420 32206050 · DOI
- [170]Graney PL, Ben-Shaul S, Landau S, et al. Macrophages of diverse phenotypes drive vascularization of engineered tissues. Sci Adv. 2020; 6: eaay6391. American Association for the Advancement of Science. doi: 10.1126/sciadv.aay6391 32494664 PMC7195167 · DOI
- [171]de Hilster RHJ, Sharma PK, Jonker MR, et al. Human lung extracellular matrix hydrogels resemble the stiffness and viscoelasticity of native lung tissue. Am J Physiol Lung Cell Mol Physiol. 2020; 318: L698– L704. American Physiological Society Bethesda, MD. doi: 10.1152/ajplung.00451.2019 32048864 PMC7191637 · DOI
- [172]Campillo N, Jorba I, Schaedel L, et al. A novel chip for cyclic stretch and intermittent hypoxia cell exposures mimicking obstructive sleep apnea. Front Physiol. 2016; 7: 319. Frontiers. doi: 10.3389/fphys.2016.00319 27524971 PMC4965455 · DOI
- [173]Da Palma RK, Nonaka PN, Campillo N, et al. Behavior of vascular resistance undergoing various pressure insufflation and perfusion on decellularized lungs. J Biomech. 2016; 49: 1230– 1232. Elsevier. doi: 10.1016/j.jbiomech.2016.02.043 26949099 · DOI
- [174]Linville RM, Boland NF, Covarrubias G, Price GM, Tien J. Physical and chemical signals that promote vascularization of capillary-scale channels. Cell Mol Bioeng. 2016; 9: 73– 84. Springer. doi: 10.1007/s12195-016-0429-8 27110295 PMC4838400 · DOI
- [175]Senger D, Davis G. Angiogenesis. Cold Spring Harb Perspect Biol. 2011; 3(8): a005090. doi: 10.1101/cshperspect.a005090 21807843 PMC3140681 · DOI
- [176]Bramfeld H, Sabra G, Centis V, Vermette P. Scaffold vascularization: a challenge for three-dimensional tissue engineering. Curr Med Chem. 2010; 17: 3944– 3967. Bentham Science Publishers. doi: 10.2174/092986710793205327 20939827 · DOI
- [177]Buchanan CF, Verbridge SS, Vlachos PP, Rylander MN. Flow shear stress regulates endothelial barrier function and expression of angiogenic factors in a 3D microfluidic tumor vascular model. Cell Adh Migr. 2014; 8: 517– 524. Taylor & Francis. doi: 10.4161/19336918.2014.970001 25482628 PMC4594487 · DOI · Paper page
- [178]Gladman SJ, Ward RE, Michael-Titus AT, Knight MM, Priestley JV. The effect of mechanical strain or hypoxia on cell death in subpopulations of rat dorsal root ganglion neurons in vitro. Neuroscience. 2010; 171: 577– 587. Elsevier. doi: 10.1016/j.neuroscience.2010.07.009 20674687 · DOI
- [179]Liang X, Huang X, Zhou Y, Jin R, Li Q. Mechanical stretching promotes skin tissue regeneration via enhancing mesenchymal stem cell homing and transdifferentiation. Stem Cells Transl Med. 2016; 5: 960– 969. Wiley Online Library. doi: 10.5966/sctm.2015-0274 27130223 PMC4922851 · DOI
- [180]Zhao J, Nishimura Y, Kimura A, et al. Chemokines protect vascular smooth muscle cells from cell death induced by cyclic mechanical stretch. Sci Rep. 2017; 7(1): 1– 9. doi: 10.1038/s41598-016-0028-x 29170451 PMC5701048 · DOI · Paper page
- [181]Ott HC, Clippinger B, Conrad C, et al. Regeneration and orthotopic transplantation of a bioartificial lung. Nat Med. 2010; 16: 927– 933. Nature Publishing Group. doi: 10.1038/nm.2193 20628374 · DOI · Paper page
- [182]Kang Y, Chang J. Channels in a porous scaffold: a new player for vascularization. Regen Med. 2018; 13: 705– 715. Future Medicine. doi: 10.2217/rme-2018-0022 30246614 · DOI
- [183]Perng C-K, Wang Y-J, Tsi C-H, Ma H. In vivo angiogenesis effect of porous collagen scaffold with hyaluronic acid oligosaccharides. J Surg Res. 2011; 168: 9– 15. Elsevier. doi: 10.1016/j.jss.2009.09.052 20080258 · DOI
- [184]Mehdizadeh H, Bayrak ES, Lu C, et al. Agent-based modeling of porous scaffold degradation and vascularization: optimal scaffold design based on architecture and degradation dynamics. Acta Biomater. 2015; 27: 167– 178. Elsevier. doi: 10.1016/j.actbio.2015.09.011 26363375 · DOI
- [185]Graham HK, McConnell JC, Limbert G, Sherratt MJ. How stiff is skin? Exp Dermatol. 2019; 28: 4– 9. doi: 10.1111/exd.13826 30698873 · DOI
- [186]Handorf AM, Zhou Y, Halanski MA, Li W-J. Tissue stiffness dictates development, homeostasis, and disease progression. Organogenesis. 2015; 11(1): 1– 15. doi: 10.1080/15476278.2015.1019687 25915734 PMC4594591 · DOI
- [187]Murphy MC, Huston III, Jack J Jr, et al. Measuring the characteristic topography of brain stiffness with magnetic resonance elastography. PLoS One. 2013; 8(12): e81668. doi: 10.1371/journal.pone.0081668 24312570 PMC3847077 · DOI
- [188]Liu L, You Z, Yu H, et al. Mechanotransduction-modulated fibrotic microniches reveal the contribution of angiogenesis in liver fibrosis. Nat Mater. 2017; 16: 1252– 1261. Nature Publishing Group. doi: 10.1038/nmat5024 29170554 · DOI · Paper page
- [189]Ren Y, Zhan Q, Hu Q, Sun B, Yang C, Wang C. Static stretch induces active morphological remodeling and functional impairment of alveolar epithelial cells. Respiration. 2009; 78: 301– 311. Karger Publishers. doi: 10.1159/000207632 19270436 · DOI
- [190]Stabler CT, Caires L Jr, Mondrinos C, et al. Enhanced re-endothelialization of decellularized rat lungs. Tissue Eng Part C Methods. 2016; 22: 439– 450. Mary Ann Liebert, Inc. 140 Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA. doi: 10.1089/ten.tec.2016.0012 26935764 PMC4870653 · DOI
- [191]Ruehle MA, Eastburn EA, LaBelle SA, et al. Extracellular matrix compression temporally regulates microvascular angiogenesis. Sci Adv. 2020; 6: eabb6351. American Association for the Advancement of Science. doi: 10.1126/sciadv.abb6351 32937368 PMC7442478 · DOI
- [192]Hauser S, Jung F, Pietzsch J. Human endothelial cell models in biomaterial research. Trends Biotechnol. 2017; 35(3): 265– 277. doi: 10.1016/j.tibtech.2016.09.007 27789063 · DOI
- [193]Narayan D, Venkatraman SS. Effect of pore size and interpore distance on endothelial cell growth on polymers. J Biomed Mater Res A. 2008; 87: 710– 718. Wiley Online Library. doi: 10.1002/jbm.a.31749 18200559 · DOI
- [194]Narmoneva DA, Oni O, Sieminski AL, et al. Self-assembling short oligopeptides and the promotion of angiogenesis. Biomaterials. 2005; 26: 4837– 4846. Elsevier. doi: 10.1016/j.biomaterials.2005.01.005 15763263 · DOI
- [195]Mirabella T, MacArthur JW, Cheng D, et al. 3D-printed vascular networks direct therapeutic angiogenesis in ischaemia. Nat Biomed Eng. 2017; 1: 1– 8. Nature Publishing Group. doi: 10.1038/s41551-017-0083 PMC5837070 29515935 · DOI
- [196]Sart S, Agathos SN, Li Y. Engineering stem cell fate with biochemical and biomechanical properties of microcarriers. Biotechnol Prog. 2013; 29: 1354– 1366. Wiley Online Library. doi: 10.1002/btpr.1825 24124017 · DOI
- [197]Edgar L, Pu T, Porter B, et al. Regenerative medicine, organ bioengineering and transplantation. J Br Surg. 2020; 107: 793– 800. Oxford University Press. doi: 10.1002/bjs.11686 32463143 · DOI
- [198]Narayan R, Agarwal T, Mishra D, Maiti TK, Mohanty S. Goat tendon collagen-human fibrin hydrogel for comprehensive parametric evaluation of HUVEC microtissue-based angiogenesis. Colloids Surf B Biointerfaces. 2018; 163: 291– 300. doi: 10.1016/j.colsurfb.2017.12.056 29329074 · DOI
- [199]Mammoto A, Connor KM, Mammoto T, et al. A mechanosensitive transcriptional mechanism that controls angiogenesis. Nature. 2009; 457(7233): 1103– 1108. doi: 10.1038/nature07765 19242469 PMC2708674 · DOI
- [200]Xiao X, Wang W, Liu D, et al. The promotion of angiogenesis induced by three-dimensional porous beta-tricalcium phosphate scaffold with different interconnection sizes via activation of PI3K/Akt pathways. Sci Rep. 2015; 5: 1– 11. Nature Publishing Group. PMC4369742 25797242
- [201]Lee J-H, Parthiban P, Jin G-Z, Knowles JC, Kim H-W. Materials roles for promoting angiogenesis in tissue regeneration. Prog Mater Sci. 2021; 117: 100732.
200 of 204 shown
Cited by
Sorted by citations
Resorbable Biomaterials Used for 3D Scaffolds in Tissue Engineering: A Review
Vach Agocsova, S., Culenova, M., Birova, I., Omanikova, L., Moncmanova, B., Danisovic, L., Ziaran, S., Bakos, D., & Alexy, P. (2023) · Materials · doi:10.3390/ma16124267 · Cited by 98 · see citing works
- Authors
- Shokrani, H., Shokrani, A., Sajadi, S. M., Seidi, F., Mashhadzadeh, A. H., Rabiee, N., Saeb, M. R., Aminabhavi, T., & Webster, T. J.
- Affiliations
- Sharif University of Technology (IR)
- Cihan University-Erbil (IQ)
- Nanjing Forestry University (CN)
- Nazarbayev University (KZ)
- Gdańsk University of Technology (PL)
- Karnatak University (IN)
- Hebei University (CN)
- Corresponding author
- Sajadi, S Mohammad
- ORCID
- Venue
- International Journal of Nanomedicine
- Publisher
- Informa UK Limited
- Published
- 2022-03
- Volume
- Volume 17
- Pages
- 1035-1068
- ISSN
- 1176-9114 (ISSN-L)
- 1178-2013
- PMC
- PMC8927652
- OpenAlex
- W4221063411
- Cited by
- 48
- References
- 1
- Citations by year
- 2026: 7 · 2025: 10 · 2024: 6 · 2023: 12 · 2022: 13
- FWCI
- 0.75
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- International Journal of Nanomedicine (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Nazarbayev University Repository (Nazarbayev University) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Dove Medical Press (Taylor and Francis Group) (submittedVersion, cc-by-nc)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
- Keywords
- angiogenesis, cell-seeded scaffolds, neovascularization, biomaterial scaffolds, hydrogels, cell sources, biomechanical stimulation, electrical stimulation, topographical cues, magnetic stimulation, scaffold biocompatibility, scaffold degradation, tissue engineering
- MeSH terms
- Biocompatible Materials, Neovascularization, Physiologic, Hydrogels, Tissue Engineering, Tissue Scaffolds
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