Caveolae, caveolins, and cavins: complex control of cellular signalling and inflammation

Lipid rafts and signal transduction

Simons, K., & Toomre, D. (2000) · Nature Reviews Molecular Cell Biology · doi:10.1038/35036052 · Cited by 5,371

Loss of Caveolae, Vascular Dysfunction, and Pulmonary Defects in Caveolin-1 Gene-Disrupted Mice

Dráb, M., Verkade, P., Elger, M., Kasper, M. E., Löhn, M., Lauterbach, B., Menne, J., Lindschau, C., Mende, F., Luft, F. C., et al. (2001) · Science · doi:10.1126/science.1062688 · Cited by 1,555

Caveolin-1 Null Mice Are Viable but Show Evidence of Hyperproliferative and Vascular Abnormalities

Razani, B., Engelman, J. A., Wang, X., Schubert, W., Zhang, X. L., Marks, C. B., Macaluso, F., Russell, R. G., Li, M., Pestell, R. G., et al. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105408200 · Cited by 1,186

Caveolins, Liquid-Ordered Domains, and Signal Transduction

Smart, E. J., Graf, G. A., McNiven, M. A., Sessa, W. C., Engelman, J. A., Scherer, P. E., Okamoto, T., & Lisanti, M. P. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.11.7289 · Cited by 1,005

Unbiased quantitative proteomics of lipid rafts reveals high specificity for signaling factors

Foster, L. J., de Hoog, C. L., & Mann, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0631608100 · Cited by 834

THE FINE STRUCTURE OF THE GALL BLADDER EPITHELIUM OF THE MOUSE

Yamada, E. (1955) · The Journal of Cell Biology · doi:10.1083/jcb.1.5.445 · Cited by 831

Dissecting the Interaction between Nitric Oxide Synthase (NOS) and Caveolin

Garcı́a-Cardeña, G., Martasek, P., Masters, B. S. S., Skidd, P. M., Couet, J., Li, S., Lisanti, M. P., & Sessa, W. C. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.41.25437 · Cited by 821

The Adaptor Protein Shc Couples a Class of Integrins to the Control of Cell Cycle Progression

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PTRF-Cavin, a conserved cytoplasmic protein required for caveola formation and function.

Hill, M., Bastiani, M., Luetterforst, R., Kirkham, M., Kirkham, A., Nixon, S. J., Walser, P., Abankwa, D., Oorschot, V., Martin, S., et al. (2008) · Cell · doi:10.1016/j.cell.2007.11.042 · Cited by 739

Potocytosis: Sequestration and Transport of Small Molecules by Caveolae

Anderson, R. G. W., Kamen, B. A., Rothberg, K. G., & Lacey, S. W. (1992) · Science · doi:10.1126/science.1310359 · Cited by 734

Angiotensin II Signal Transduction: An Update on Mechanisms of Physiology and Pathophysiology

Forrester, S. J., Booz, G. W., Sigmund, C. D., Coffman, T. M., Kawai, T., Rizzo, V., Scalia, R. G., & Eguchi, S. (2018) · Physiological Reviews · doi:10.1152/physrev.00038.2017 · Cited by 1,135

Mechanotransduction in Cardiac Hypertrophy and Failure

Lyon, R. C., Zanella, F., Omens, J. H., & Sheikh, F. (2015) · Circulation Research · doi:10.1161/circresaha.116.304937 · Cited by 356

Role of reactive oxygen and nitrogen species in the vascular responses to inflammation

Kvietys, P. R., & Granger, D. N. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.11.002 · Cited by 319

A Comparison of Cellular Uptake Mechanisms, Delivery Efficacy, and Intracellular Fate between Liposomes and Extracellular Vesicles

Gandek, T. B., van der Koog, L., & Nagelkerke, A. (2023) · Advanced Healthcare Materials · doi:10.1002/adhm.202300319 · Cited by 256

STRIPAK complexes: Structure, biological function, and involvement in human diseases

Hwang, J., & Pallas, D. C. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.11.021 · Cited by 234

Cavin family proteins and the assembly of caveolae

Kovtun, O., Tillu, V. A., Ariotti, N., Parton, R. G., & Collins, B. M. (2015) · Journal of Cell Science · doi:10.1242/jcs.167866 · Cited by 230

Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects

Machado, R. D., Southgate, L., Eichstaedt, C. A., Aldred, M. A., Austin, E. D., Best, D. H., Chung, W. K., Benjamin, N., Elliott, C. G., Eyries, M., et al. (2015) · Human Mutation · doi:10.1002/humu.22904 · Cited by 227

Chemoprevention of liver cancer by plant polyphenols

Stagos, D., Amoutzias, G. D., Matakos, A., Spyrou, A., Tsatsakis, A. M., & Kouretas, D. (2012) · Food and Chemical Toxicology · doi:10.1016/j.fct.2012.04.002 · Cited by 197

EDHF: spreading the influence of the endothelium

Garland, C. J., Hiley, C. R., & Dora, K. A. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.01148.x · Cited by 195

Flavonoid–membrane interactions: Involvement of flavonoid–metal complexes in raft signaling

Tarahovsky, Y. S., Kim, Y. A., АНДРЕЕВНА, Я. Е., & Muzafarov, E. N. (2014) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2014.01.021 · Cited by 199

Cellular Uptake and Intracellular Trafficking of Antisense and siRNA Oligonucleotides

Juliano, R. L., Ming, X., & Nakagawa, O. (2012) · Bioconjugate Chemistry · doi:10.1021/bc200377d · Cited by 181

The Genetics of Pulmonary Arterial Hypertension

Austin, E. D., & Loyd, J. E. (2014) · Circulation Research · doi:10.1161/circresaha.115.303404 · Cited by 193

Understanding Angiotensin II Type 1 Receptor Signaling in Vascular Pathophysiology

Eguchi, S., Kawai, T., Scalia, R., & Rizzo, V. (2018) · Hypertension · doi:10.1161/hypertensionaha.118.10266 · Cited by 189

Regulation of Endothelial Barrier Function

Yuan, S. Y., & Rigor, R. R. (2011) · Colloquium Series on Integrated Systems Physiology From Molecule to Function · doi:10.4199/c00025ed1v01y201101isp013 · Cited by 188

Endothelial NOS: perspective and recent developments

Garcia, V. G., & Sessa, W. C. (2018) · British Journal of Pharmacology · doi:10.1111/bph.14522 · Cited by 184

Cytokine‐mediated blood brain barrier disruption as a conduit for cancer/chemotherapy‐associated neurotoxicity and cognitive dysfunction

Wardill, H. R., Mander, K. A., Sebille, Y. Z. A. V., Gibson, R. J., Logan, R. M., Bowen, J. M., & Sonis, S. T. (2016) · International Journal of Cancer · doi:10.1002/ijc.30252 · Cited by 182

Endothelial Transcytosis of Lipoproteins in Atherosclerosis

Zhang, X., Sessa, W. C., & Fernandez-Hernando, C. F. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00130 · Cited by 158

Into rather unexplored terrain—transcellular transport across the blood–brain barrier

Bock, M. D., Haver, V. V., Vandenbroucke, R. E., Decrock, E., Wang, N., & Leybaert, L. (2016) · Glia · doi:10.1002/glia.22960 · Cited by 159

Stressing caveolae new role in cell mechanics

Nassoy, P., & Lamaze, C. (2012) · Trends in Cell Biology · doi:10.1016/j.tcb.2012.04.007 · Cited by 155

Proteomic Analysis of Lung Tissues From Patients With Pulmonary Arterial Hypertension

Abdul‐Salam, V. B., Wharton, J., Cupitt, J., Berryman, M. A., Edwards, R. J., & Wilkins, M. R. (2010) · Circulation · doi:10.1161/circulationaha.110.972745 · Cited by 132

Caveolin‐1, cancer and therapy resistance

Ketteler, J., & Klein, D. (2018) · International Journal of Cancer · doi:10.1002/ijc.31369 · Cited by 129

Prolonged sleep restriction induces changes in pathways involved in cholesterol metabolism and inflammatory responses

Aho, V., Ollila, H. M., Kronholm, E., Bondia-Pons, I., Soininen, P., Kangas, A. J., Hilvo, M., Seppälä, I., Kettunen, J., Oikonen, M., et al. (2016) · Scientific Reports · doi:10.1038/srep24828 · Cited by 126

Tollip: a multitasking protein in innate immunity and protein trafficking

Capelluto, D. G. S. (2011) · Microbes and Infection · doi:10.1016/j.micinf.2011.08.018 · Cited by 118

Basic physiology of the blood-brain barrier in health and disease: a brief overview

Kaya, M., & Ahıshalı, B. (2020) · Tissue Barriers · doi:10.1080/21688370.2020.1840913 · Cited by 126

Nitric oxide-matrix metaloproteinase-9 interactions: Biological and pharmacological significance

O’Sullivan, S., Medina, C., Ledwidge, M. T., Radomski, M. W., & Gilmer, J. F. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.12.006 · Cited by 117

Caveolae: The FAQs

Parton, R. G., del Pozo, M. Á., Vassilopoulos, S., Nabi, I. R., Lay, S. L., Lundmark, R., Kenworthy, A. K., Camus, A., Blouin, C. M., Sessa, W. C., et al. (2019) · Traffic · doi:10.1111/tra.12689 · Cited by 107

Adiponectin Inhibits Tumor Necrosis Factor-α–Induced Vascular Inflammatory Response via Caveolin-Mediated Ceramidase Recruitment and Activation

Wang, Y., Wang, X., Lau, W. B., Yuan, Y., Booth, D., Li, J.-J., Scalia, R., Preston, K., Gao, E., Koch, W., et al. (2014) · Circulation Research · doi:10.1161/circresaha.114.302439 · Cited by 104

A review of the role of cav-1 in neuropathology and neural recovery after ischemic stroke

Huang, Q., Zhong, W., Hu, Z., & Tang, X. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1387-y · Cited by 102

Caveolin-1 is a negative regulator of NADPH oxidase-derived reactive oxygen species

Chen, F., Barman, S. A., Yu, Y., Haigh, S., Wang, Y., Dou, H., Bagi, Z. A., Han, W., Su, Y., & Fulton, D. J. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.04.029 · Cited by 99

Subcellular trafficking of the substrate transporters GLUT4 and CD36 in cardiomyocytes

Steinbusch, L. K. M., Schwenk, R. W., Ouwens, D. M., Diamant, M., Glatz, J. F. C., & Luiken, J. J. F. P. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0690-x · Cited by 99

Supported Lipid Bilayers for the Generation of Dynamic Cell–Material Interfaces

van Weerd, J., Karperien, M., & Jonkheijm, P. (2015) · Advanced Healthcare Materials · doi:10.1002/adhm.201500398 · Cited by 93

Traumatic brain injury enhances neuroinflammation and lesion volume in caveolin deficient mice

Niesman, I., Schilling, J., Shapiro, L. A., Kellerhals, S., Bonds, J. A., Kleschevnikov, A., Cui, W.-H., Voong, A., Krajewski, S., Ali, S., et al. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-39 · Cited by 84

Caveolin‐1 deficiency induces a MEK‐ERK1/2‐Snail‐1‐dependent epithelial–mesenchymal transition and fibrosis during peritoneal dialysis

Strippoli, R., Loureiro, J., Moreno, V., Benedicto, I., Lozano, M. L. P., Barreiro, O., Pellinen, T. S., Minguet, S., Foronda, M., Osteso-Ibáñez, T., et al. (2014) · EMBO Molecular Medicine · doi:10.15252/emmm.201404127 · Cited by 92

Caveolin-1 in the Anterior Cingulate Cortex Modulates Chronic Neuropathic Pain via Regulation of NMDA Receptor 2B Subunit

Yang, J., Hua, L., Li, Y., Jiang, Y., Han, D. K., Liu, H., Tang, Q., Yang, X.-N., Cui, Y., Hao, L.-Y., et al. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1161-14.2015 · Cited by 90

Caveolin-1 Inhibits Expression of Antioxidant Enzymes through Direct Interaction with Nuclear Erythroid 2 p45-related Factor-2 (Nrf2)

Li, W., Liu, H., Zhou, J.-S., Cao, J.-F., Zhou, X.-B., Choi, A. M. K., Chen, Z.-H., & Shen, H. H. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.352336 · Cited by 89

Targeting RNS/caveolin-1/MMP signaling cascades to protect against cerebral ischemia-reperfusion injuries: potential application for drug discovery

Chen, H., Chen, X., Li, W., & Shen, J. (2018) · Acta Pharmacologica Sinica · doi:10.1038/aps.2018.27 · Cited by 86

Sevoflurane Preconditioning Attenuates Myocardial Ischemia/Reperfusion Injury via Caveolin-3–Dependent Cyclooxygenase-2 Inhibition

Zhao, J., Wang, F., Zhang, Y., Jiao, L., Lau, W. B., Wang, L., Liu, B., Gao, E., Koch, W. J., Ma, X., et al. (2013) · Circulation · doi:10.1161/circulationaha.112.000045 · Cited by 84

Interaction of caveolin-1 with ATG12-ATG5 system suppresses autophagy in lung epithelial cells

Chen, Z., Cao, J., Zhou, J.-S., Liu, H., Che, L., Mizumura, K., Li, W., Choi, A. M. K., & Shen, H. (2014) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00268.2013 · Cited by 86

Sphingolipids: agents provocateurs in the pathogenesis of insulin resistance

Lipina, C., & Hundal, H. S. (2011) · Diabetologia · doi:10.1007/s00125-011-2127-3 · Cited by 83

The emerging role of tetraspanin microdomains on endothelial cells

Bailey, R. L., Herbert, J. M. J., Khan, K. A., Heath, V. L., Bicknell, R., & Tomlinson, M. G. (2011) · Biochemical Society Transactions · doi:10.1042/bst20110745 · Cited by 83

Caveolins and caveolae in ocular physiology and pathophysiology

Gu, X., Reagan, A. M., McClellan, M. E., & Elliott, M. H. (2016) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2016.09.005 · Cited by 81

Facing glycosphingolipid–Shiga toxin interaction: dire straits for endothelial cells of the human vasculature

Bauwens, A., Betz, J., Meisen, I., Kemper, B., Karch, H., & Müthing, J. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1060-z · Cited by 80

1α,25(OH)2D3‐dependent modulation of Akt in proliferating and differentiating C2C12 skeletal muscle cells

Buitrago, C., Arango, N. S., & Boland, R. (2011) · Journal of Cellular Biochemistry · doi:10.1002/jcb.23444 · Cited by 79

Caveolin-1 regulation of store-operated Ca2+influx in human airway smooth muscle

Sathish, V., Abcejo, A. J., Thompson, M. A., Sieck, G. C., Prakash, Y. S., & Pabelick, C. M. (2012) · European Respiratory Journal · doi:10.1183/09031936.00090511 · Cited by 78

EHD Proteins Cooperate to Generate Caveolar Clusters and to Maintain Caveolae during Repeated Mechanical Stress

Yeow, I., Howard, G., Chadwick, J., Mendoza-Topaz, C., Hansen, C. G., Nichols, B. J., & Shvets, E. (2017) · Current Biology · doi:10.1016/j.cub.2017.07.047 · Cited by 84

Treadmill exercise promotes angiogenesis in the ischemic penumbra of rat brains through caveolin-1/VEGF signaling pathways

Gao, Y., Zhao, Y., Pan, J., Liu, Y., Huang, T., Feng, X., Li, C., Liang, S., Zhou, D., Liu, C., et al. (2014) · Brain Research · doi:10.1016/j.brainres.2014.08.032 · Cited by 77

Membrane Glucocorticoid Receptor Activation Induces Proteomic Changes Aligning with Classical Glucocorticoid Effects

Vernocchi, S., Battello, N., Schmitz, S., Revets, D., Billing, A. M., Turner, J. D., & Muller, C. P. (2013) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m112.022947 · Cited by 75

Role of extracellular calcium and mitochondrial oxygen species in psychosine-induced oligodendrocyte cell death

Voccoli, V., Tonazzini, I., Signore, G., Caleo, M., & Cecchini, M. G. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.483 · Cited by 70

Mechanisms and functions of endocytosis in T cells

Charpentier, J. C., & King, P. D. (2021) · Cell Communication and Signaling · doi:10.1186/s12964-021-00766-3 · Cited by 69

Immune responses at brain barriers and implications for brain development and neurological function in later life

Stolp, H. B., Liddelow, S. A., Sá-Pereira, I., Dzięgielewska, K. M., & Saunders, N. R. (2013) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2013.00061 · Cited by 73

LDL receptors, caveolae and cholesterol in endothelial dysfunction: oxLDLs accomplices or victims?

Luchetti, F., Crinelli, R., Nasoni, M. G., Benedetti, S., Palma, F., Fraternale, A., & Iuliano, L. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15272 · Cited by 72

The Deleterious Effects of Oxidative and Nitrosative Stress on Palmitoylation, Membrane Lipid Rafts and Lipid-Based Cellular Signalling: New Drug Targets in Neuroimmune Disorders

Morris, G., Walder, K. R., Puri, B. K., Berk, M., & Maes, M. H. J. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9392-y · Cited by 70

Endocytosis, intracellular fate, accumulation, and agglomeration of titanium dioxide (TiO2) nanoparticles in the rainbow trout liver cell line RTL-W1

Lammel, T., Mackevica, A., Johansson, B. R., & Sturve, J. (2019) · Environmental Science and Pollution Research · doi:10.1007/s11356-019-04856-1 · Cited by 62

Caveolin-1 Deletion Prevents Hypertensive Vascular Remodeling Induced by Angiotensin II

Forrester, S. J., Elliott, K. J., Kawai, T., Obama, T., Boyer, M. J., Preston, K. J., Yan, Z., Eguchi, S., & Rizzo, V. (2016) · Hypertension · doi:10.1161/hypertensionaha.116.08278 · Cited by 61

New insights into exosome mediated tumor-immune escape: Clinical perspectives and therapeutic strategies

Pathania, A. S., Prathipati, P., & Challagundla, K. B. (2021) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2021.188624 · Cited by 62

Heme Oxygenase-1 Regulates Dendritic Cell Function through Modulation of p38 MAPK-CREB/ATF1 Signaling

Al-Huseini, L. M. A., Yeang, H. X. A., Hamdam, J. M., Sethu, S., Alhumeed, N., Wong, W., & Sathish, J. G. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.532069 · Cited by 60

Endothelial membrane reorganization during leukocyte extravasation

Reglero-Real, N., Marcos‐Ramiro, B., & Millán, J. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-0987-4 · Cited by 56

Caveolin-1 Deficiency Induces Spontaneous Endothelial-to-Mesenchymal Transition in Murine Pulmonary Endothelial Cells in Vitro

Li, Z., Wermuth, P. J., Benn, B. S., Lisanti, M. P., & Jiménez, S. A. (2012) · American Journal Of Pathology · doi:10.1016/j.ajpath.2012.10.022 · Cited by 58

Effects of Treadmill Exercise on Motor and Cognitive Function Recovery of MCAO Mice Through the Caveolin-1/VEGF Signaling Pathway in Ischemic Penumbra

Chen, Z., Hu, Q., Xie, Q., Wu, S., Pang, Q., Liu, M., Zhao, Y., Tu, F., Liu, C., & Chen, X. '. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02728-1 · Cited by 53

Cellular Prion Protein (PrPc): Putative Interacting Partners and Consequences of the Interaction

Miranzadeh Mahabadi, H., & Taghibiglou, C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197058 · Cited by 52

miR-96-5p promotes the proliferation and migration of ovarian cancer cells by suppressing Caveolae1

Liu, B., Zhang, J., & Yang, D. (2019) · Journal of Ovarian Research · doi:10.1186/s13048-019-0533-1 · Cited by 52

Caveolin 1 is critical for abdominal aortic aneurysm formation induced by angiotensin II and inhibition of lysyl oxidase

Takayanagi, T., Crawford, K., Kobayashi, T., Obama, T., Tsuji, T., Elliott, K. J., Hashimoto, T. N., Rizzo, V., & Eguchi, S. (2013) · Clinical Science · doi:10.1042/cs20130660 · Cited by 51

Drugs Involved in Dyslipidemia and Obesity Treatment: Focus on Adipose Tissue

Dias, S., Paredes, S., & Ribeiro, L. V. P. T. (2018) · International Journal of Endocrinology · doi:10.1155/2018/2637418 · Cited by 51

Caveolin-1: an essential modulator of cancer cell radio-and chemoresistance.

Hehlgans, S., & Cordes, N. (2011) · Europe PMC (PubMed Central) · Cited by 51

Cortical Actin Dynamics in Endothelial Permeability

Belvitch, P. G., Htwe, Y. M., Brown, M. E., & Dudek, S. M. (2018) · Current topics in membranes · doi:10.1016/bs.ctm.2018.09.003 · Cited by 54

Caveolin‐1 deficiency decreases atherosclerosis by hampering leukocyte influx into the arterial wall and generating a regulatory T‐cell response

Engel, D. A., Beckers, L., Wijnands, E., Seijkens, T. T. P., Lievens, D., Drechsler, M. D., Gerdes, N., Soehnlein, O., Daemen, M. J. A. P., Stan, R. V., et al. (2011) · The FASEB Journal · doi:10.1096/fj.11-183350 · Cited by 49

Essential Role of Caveolin-3 in Adiponectin Signalsome Formation and Adiponectin Cardioprotection

Wang, Y., Wang, X., Jasmin, J.-F., Lau, W. B., Li, R., Yuan, Y., Yi, W., Chuprun, K. J., Lisanti, M. P., Koch, W. J., et al. (2012) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.242164 · Cited by 46

Caveolae control the anti‐inflammatory phenotype of senescent endothelial cells

Powter, E. E., Coleman, P. R., Tran, M. H., Lay, A. J., Bertolino, P., Parton, R. G., Vadas, M. A., & Gamble, J. R. (2014) · Aging Cell · doi:10.1111/acel.12270 · Cited by 48

Active induction of experimental autoimmune encephalomyelitis by MOG35-55 peptide immunization is associated with differential responses in separate compartments of the choroid plexus

Murugesan, N., Paul, D., Lemire, Y., Shrestha, B., Ge, S., & Pachter, J. S. (2012) · Fluids and Barriers of the CNS · doi:10.1186/2045-8118-9-15 · Cited by 47

Caveolar and non-Caveolar Caveolin-1 in ocular homeostasis and disease

Enyong, E. N., Gurley, J. M., Ieso, M. L. D., Stamer, W. D., & Elliott, M. H. (2022) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2022.101094 · Cited by 46

MYADM controls endothelial barrier function through ERM-dependent regulation of ICAM-1 expression

Aranda, J. F., Reglero-Real, N., Marcos‐Ramiro, B., Ruiz-Sáenz, A., Fernández‐Martín, L., Bernabé‐Rubio, M., Kremer, L., Ridley, A. J., Correas, I., Alonso, M. A., et al. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-11-0914 · Cited by 47

Caveolae and Caveolin-1 Integrate Reverse Cholesterol Transport and Inflammation in Atherosclerosis

Li, Q., Zhu, N., Ao, B.-X., Liu, C., Shi, Y., Du, K., Chen, J., Zheng, X., & Liao, D. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17030429 · Cited by 47

Caveolin-1: A Review of Intracellular Functions, Tissue-Specific Roles, and Epithelial Tight Junction Regulation

Dalton, C. M., Schlegel, C., & Hunter, C. J. (2023) · Biology · doi:10.3390/biology12111402 · Cited by 45

Genetics of pulmonary hypertension

Best, D. H., Austin, E. D., Chung, W. K., & Elliott, C. G. (2014) · Current Opinion in Cardiology · doi:10.1097/hco.0000000000000105 · Cited by 45

Selective stimulation of caveolae-mediated endocytosis by an osmotic polymannitol-based gene transporter

Park, T., Kang, B., Kim, Y.-K., Zhang, Q., Lee, W., Islam, M. A., Kang, S., Cho, M., Choi, Y., & Cho, C. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.06.037 · Cited by 45

Interleukin-1 Assembles a Proangiogenic Signaling Module Consisting of Caveolin-1, Tumor Necrosis Factor Receptor–Associated Factor 6, p38–Mitogen-Activated Protein Kinase (MAPK), and MAPK-Activated Protein Kinase 2 in Endothelial Cells

Jagielska, J., Kapopara, P. R., Salguero, G., Scherr, M., Schütt, H., Grote, K., Schieffer, B., & Bavendiek, U. (2012) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.243477 · Cited by 45

Critical role of caveolin-1 in ocular neovascularization and multitargeted antiangiogenic effects of cavtratin via JNK

Jiang, Y., Lin, X., Tang, Z., Lee, C., Tian, G., Du, Y., Yin, X., Ren, X., Huang, L., Ye, Z., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1706394114 · Cited by 44

Simvastatin Improves Microcirculatory Function in Nonalcoholic Fatty Liver Disease and Downregulates Oxidative and ALE-RAGE Stress

Pereira, E. N. G. D. S., de Araujo, B. P., Rodrigues, K. L., Silvares, R. R., Martins, C. S. M., Flores, E. E. I., Fernandes‐Santos, C., & Daliry, A. (2022) · Nutrients · doi:10.3390/nu14030716 · Cited by 43

Caveolin-1, a novel player in cognitive decline

Tang, W., Li, Y., Li, Y., & Wang, Q. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.06.044 · Cited by 43

Melatonin: Regulation of Biomolecular Condensates in Neurodegenerative Disorders

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