The DOI matches its Crossref record; 213 of the 213 references it cites were found in a registry or an index.
Mitochondria and Endothelial Function
Open accessAbstract
In contrast to their role in cell types with higher energy demands, mitochondria in endothelial cells primarily function in signaling cellular responses to environmental cues. This article provides an overview of key aspects of mitochondrial biology in endothelial cells, including subcellular location, biogenesis, dynamics, autophagy, reactive oxygen species production and signaling, calcium homeostasis, regulated cell death, and heme biosynthesis. In each section, we introduce key concepts and then review studies showing the importance of that mechanism to endothelial control of vasomotor tone, angiogenesis, and/or inflammatory activation. We particularly highlight the small number of clinical and translational studies that have investigated each mechanism in human subjects. Finally, we review interventions that target different aspects of mitochondrial function and their effects on endothelial function. The ultimate goal of such research is the identification of new approaches for therapy. The reviewed studies make it clear that mitochondria are important in endothelial physiology and pathophysiology. A great deal of work will be needed, however, before mitochondria-directed therapies are available for the prevention and treatment of cardiovascular disease.
Overview
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.
Integrity signals
Registry
Cites
Statistics
Verification
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.
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?
In the citing paper
“Accumulating evidence implicates mitochondrial dysregulation in impaired arterial function both in animal models of cardiovascular disease (94, 161, 182)”
From Inorganic nitrite supplementation for healthy arterial aging (2014) · cites this paper as [94]
In the citing paper
“If metformin can offset the decline in mitochondrial function, as some studies suggest, then this effect could contribute to enhancing both healthspan and lifespan (138, 149, 150).”
From A Critical Review of the Evidence That Metformin Is a Putative Anti-Aging Drug That Enhances Healthspan and Extends Lifespan (2021) · cites this paper as [149]
In the citing paper
“AMPK has also been implicated in the regulation of mitochondrial biogenesis, thus providing another link between metformin, AMPK, and improved mitochondrial function (149, 150).”
From A Critical Review of the Evidence That Metformin Is a Putative Anti-Aging Drug That Enhances Healthspan and Extends Lifespan (2021) · cites this paper as [149]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Apoptosis: A Review of Programmed Cell Death
Elmore, S. (2007) · Toxicologic Pathology · doi:10.1080/01926230701320337 · Cited by 13,853
Mootha, V. K., Lindgren, C. M., Eriksson, K.-F., Subramanian, A., Sihag, S., Lehar, J., Puigserver, P., Carlsson, E., Ridderstråle, M., Laurila, E., et al. (2003) · Nature Genetics · doi:10.1038/ng1180 · Cited by 10,197
Biochemistry and molecular cell biology of diabetic complications
Brownlee, M. (2001) · Nature · doi:10.1038/414813a · Cited by 9,107
How mitochondria produce reactive oxygen species
Murphy, M. P. (2009) · Biochemical Journal · doi:10.1042/bj20081386 · Cited by 8,207
Hydroperoxide metabolism in mammalian organs.
Chance, B., Sies, H., & Boveris, A. (1979) · Physiological Reviews · doi:10.1152/physrev.1979.59.3.527 · Cited by 5,827
The BCL-2 protein family: opposing activities that mediate cell death
Youle, R. J., & Strasser, A. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2308 · Cited by 4,806
Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage
Nishikawa, T., Edelstein, D., Du, X. L., Yamagishi, S.-I., Matsumura, T., Kaneda, Y., Yorek, M. A., Beebe, D., Oates, P. J., Hammes, H.-P., et al. (2000) · Nature · doi:10.1038/35008121 · Cited by 4,277
Therapeutic potential of resveratrol: the in vivo evidence
Baur, J. A., & Sinclair, D. A. (2006) · Nature Reviews Drug Discovery · doi:10.1038/nrd2060 · Cited by 3,958
Youle, R. J., & Narendra, D. P. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3028 · Cited by 3,273
Nutrient control of glucose homeostasis through a complex of PGC-1α and SIRT1
Rodgers, J. T., Lerin, C., Haas, W., Gygi, S. P., Spiegelman, B. M., & Puigserver, P. (2005) · Nature · doi:10.1038/nature03354 · Cited by 3,160
Research works printed but not linked: 1
- 10.1161/circ.126.suppl_21.A16000 · DOI
Cited by
Sorted by citations
Items 101–200 of 508
Prevention and endothelial therapy of coronary artery disease
Barton, M. (2013) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2013.05.005 · Cited by 68
Kahveci, A. S., Barnatan, T. T., Kahveci, A., Adrian, A. E., Arroyo, J., Eirin, A., Harris, P. C., Lerman, A., Lerman, L. O., Torres, V. E., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21061994 · Cited by 62
Sun, J. M., Huang, X., Niu, C., Wang, X., Li, W., Liu, M., Wang, Y., Huang, S., Chen, X., Li, X., et al. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101811 · Cited by 62
Youn, Y. J., Kim, S. Y., Jeong, H., Ah, Y., & Yu, Y. M. (2024) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2024.101131 · Cited by 66
Kirkman, D. L., Muth, B. J., Ramick, M. G., Townsend, R. R., & Edwards, D. G. (2017) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00321.2017 · Cited by 62
Antioxidant role of autophagy in maintaining the integrity of glomerular capillaries
Matsuda, J., Namba, T., Takabatake, Y., Kimura, T., Takahashi, A., Yamamoto, T., Minami, S., Sakai, S., Fujimura, R., Kaimori, J.-Y., et al. (2018) · Autophagy · doi:10.1080/15548627.2017.1391428 · Cited by 61
Voluntary aerobic exercise increases arterial resilience and mitochondrial health with aging in mice
Gioscia‐Ryan, R. A., Battson, M. L., Cuevas, L. M., Zigler, M. C., Sindler, A. L., & Seals, D. R. (2016) · Aging · doi:10.18632/aging.101099 · Cited by 61
YAP1-TEAD1 signaling controls angiogenesis and mitochondrial biogenesis through PGC1α
Mammoto, A., Muyleart, M., Kadlec, A. O., Gutterman, D. D., & Mammoto, T. (2018) · Microvascular Research · doi:10.1016/j.mvr.2018.04.003 · Cited by 60
Circadian Rhythms in Cardiovascular Metabolism
Lal, H., Verma, S. K., Wang, Y., Xie, M., & Young, M. E. (2024) · Circulation Research · doi:10.1161/circresaha.123.323520 · Cited by 67
Su, L., Liu, M., Chen, J., Chen, Y., Yin, M., Zhou, Y., Li, Q., Xu, F., Li, Y., Yan, X., et al. (2023) · Acta Physiologica · doi:10.1111/apha.13975 · Cited by 58
Dave, K. M., Venna, V. R., Rao, K., Stolz, D. B., Brady, B. T., Quaicoe, V. A., Maniskas, M. E., Hildebrand, E. E., Green, D., Chen, M., et al. (2024) · Journal of Controlled Release · doi:10.1016/j.jconrel.2024.07.065 · Cited by 59
Gu, L., Ye, P., Li, H., Wang, Y., Xu, Y., Tian, Q., Lei, G., Zhao, C., Gao, Z., Zhao, W., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201802251r · Cited by 56
Sakamuri, S. S. V. P., Sure, V. N. L. R., Kolli, L., Evans, W. R., Sperling, J. A., Bix, G. J., Wang, X., Atochin, D. N., Murfee, W. L., Mostany, R., et al. (2022) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x211069266 · Cited by 55
Carresi, C., Mollace, R., Macrì, R., Scicchitano, M., Bosco, F., Scarano, F., Coppoletta, A. R., Guarnieri, L., Ruga, S., Zito, M. C., et al. (2021) · Antioxidants · doi:10.3390/antiox10030387 · Cited by 58
Endothelial FIS1 DeSUMOylation Protects Against Hypoxic Pulmonary Hypertension
Zhou, X., Jiang, Y., Wang, Y., Fan, L., Zhu, Y., Chen, Y., Wang, Y., Zhu, Y., Wang, H., Pan, Z., et al. (2023) · Circulation Research · doi:10.1161/circresaha.122.321200 · Cited by 57
Dobi, A., Rosanaly, S., Devin, A., Baret, P., Meilhac, O., Harry, G. J., d’Hellencourt, C. L., & Rondeau, P. (2020) · Microvascular Research · doi:10.1016/j.mvr.2020.104098 · Cited by 55
Busija, D. W., & Katakam, P. V. G. (2014) · Journal of Vascular Research · doi:10.1159/000360765 · Cited by 51
Kemter, E., Fröhlich, T., Arnold, G. J., Wolf, E., & Wanke, R. (2017) · Scientific Reports · doi:10.1038/srep42970 · Cited by 54
Do, P. T., Wu, C.-C., Chiang, Y. H., Hu, C., & Chen, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810045 · Cited by 57
Li, Z., Li, Q., Wang, L., Li, C., Xu, M., Duan, Y., Ma, L., Li, T., Chen, Q., Wang, Y., et al. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102156 · Cited by 54
Kozieł, A., Broniarek, I., & Jarmuszkiewicz, W. (2015) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00759.2014 · Cited by 53
Liu, H., Xiang, H., Zhao, S., Sang, H., Lv, F., Chen, R., Shu, Z., Chen, A. F., Chen, S., & Lu, H. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.13975 · Cited by 52
Exercise improves vascular health: Role of mitochondria
Zhang, X., & Gao, F. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.11.002 · Cited by 52
Molecular pathways of arterial aging
Paneni, F., Costantino, S., & Cosentino, F. (2014) · Clinical Science · doi:10.1042/cs20140302 · Cited by 53
Ko, G. H., Jin, H., Park, S. W., & Kim, H. J. (2020) · Biochemical Pharmacology · doi:10.1016/j.bcp.2020.113815 · Cited by 51
Yu, Q., & Chan, S. Y. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-63245-2_24 · Cited by 51
Laminar shear stress promotes mitochondrial homeostasis in endothelial cells
Wu, L., Chang, H., Ting, P., & Wang, D. L. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.26375 · Cited by 57
Glycosylation as new pharmacological strategies for diseases associated with excessive angiogenesis
Bousseau, S., Vergori, L., Soleti, R., Lenaers, G., Martínez, M. C., & Andriantsitohaina, R. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.06.003 · Cited by 51
Sasaki, Y., Ikeda, Y., Uchikado, Y., Akasaki, Y., Sadoshima, J., & Ohishi, M. (2021) · Journal of the American Heart Association · doi:10.1161/jaha.120.019310 · Cited by 52
Wang, W.-L., Shih, Y.-T., Wei, S.-Y., & Chiu, J.-J. (2025) · Journal of Biomedical Science · doi:10.1186/s12929-025-01177-z · Cited by 50
Yang, L., Zhang, J., Xing, W., Zhang, X., Xu, J., Zhang, H., Chen, L., Ning, X., Ji, G., Li, J., et al. (2016) · Scientific Reports · doi:10.1038/srep23366 · Cited by 50
Targeting mitochondrial fitness as a strategy for healthy vascular aging
Rossman, M. J., Gioscia‐Ryan, R. A., Clayton, Z. S., Murphy, M. P., & Seals, D. R. (2020) · Clinical Science · doi:10.1042/cs20190559 · Cited by 51
Mechanisms of cardiovascular toxicity induced by PM2.5: a review
Zhao, T., Qi, W., Pan, Y., Yang, L., Shi, Y., Zhou, L., & Ye, L. (2021) · Environmental Science and Pollution Research · doi:10.1007/s11356-021-16735-9 · Cited by 50
Dobson, G. P., Morris, J. L., & Letson, H. L. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.968453 · Cited by 51
Murray, K. O., Berryman-Maciel, M., Darvish, S., Coppock, M. E., You, Z., Chonchol, M., Seals, D. R., & Rossman, M. J. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.980783 · Cited by 48
Ye, J., Wang, S., Ge, M., & Wang, D. (2016) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00356.2015 · Cited by 48
Busija, D. W., Rutkai, I., Dutta, S., & Katakam, P. V. G. (2016) · Comprehensive physiology · doi:10.1002/cphy.c150051 · Cited by 52
Simulated microgravity‐induced mitochondrial dysfunction in rat cerebral arteries
Zhang, R., Ran, H., Cai, L., Zhu, L., Sun, J., Peng, L., Liu, X., Zhang, L. Y., Fang, Z., Fan, Y., et al. (2014) · The FASEB Journal · doi:10.1096/fj.13-245654 · Cited by 48
Hofmann, A., Mishra, J. S., Yadav, P., Dangudubiyyam, S. V., Blesson, C. S., & Kumar, S. (2023) · Journal of Environmental Science and Public Health · doi:10.26502/jesph.96120197 · Cited by 52
Oxidative stress-mediated protein sulfenylation in human diseases: Past, present, and future
Mu, B., Zeng, Y., Luo, L., & Wang, K. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103332 · Cited by 49
Mitochondrial dysfunction in endothelial cells induced by airborne fine particulate matter (<2.5 μm)
Miao, X., Li, W., Niu, B., Li, J., Sun, J., Qin, M., & Zhou, Z. (2019) · Journal of Applied Toxicology · doi:10.1002/jat.3828 · Cited by 47
Dun, Y., Liu, S., Zhang, W., Xie, M., & Qiu, L. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/8024857 · Cited by 46
Obstructive Sleep Apnea–induced Endothelial Dysfunction Is Mediated by miR-210
Shang, F., Wang, S., Gongol, B., Han, S. Y., Cho, Y., Schiavon, C. R., Chen, L., Xing, Y., Zhao, Y., Ning, M., et al. (2022) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.202202-0394oc · Cited by 46
Disturbed Flow Induces Autophagy, but Impairs Autophagic Flux to Perturb Mitochondrial Homeostasis
Li, R., Jen, N., Wu, L., Lee, J., Fang, K., Quigley, K., Lee, K. J., Wang, S., Zhou, B., Vergnes, L., et al. (2015) · Antioxidants and Redox Signaling · doi:10.1089/ars.2014.5896 · Cited by 46
Park, J.-B., Nagar, H., Choi, S., Jung, S.-B., Kim, H., Kang, S. K., Lee, J. W., Lee, J. H., Park, J., Irani, K., et al. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.02.017 · Cited by 47
Akap1 Regulates Vascular Function and Endothelial Cells Behavior
Schiattarella, G. G., Cattaneo, F., Carrizzo, A., Paolillo, R., Boccella, N., Ambrosio, M., Damato, A., Pironti, G., Franzone, A., Russo, G., et al. (2018) · Hypertension · doi:10.1161/hypertensionaha.117.10185 · Cited by 44
Anthracycline chemotherapy‐mediated vascular dysfunction as a model of accelerated vascular aging
Clayton, Z. S., Hutton, D. A., Mahoney, S. A., & Seals, D. R. (2021) · Aging and Cancer · doi:10.1002/aac2.12033 · Cited by 44
Li, G., Xu, K., Xing, W., Yang, H., Li, Y., Wang, X., Zhou, J., An, J., Dong, L., Zhang, X., et al. (2022) · Hypertension · doi:10.1161/hypertensionaha.122.19126 · Cited by 44
Francischetti, I. M. B., Gordon, E. B., Bizzarro, B., Gera, N., Andrade, B. B., Oliveira, F., Ma, D., Assumpção, T. C. F., Ribeiro, J. M. C., Peña, M., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087140 · Cited by 43
Hong, J.-M., & Lee, S. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.03.017 · Cited by 45
Protective role of the mitochondrial fusion protein OPA1 in hypertension
Robert, P., Nguyen, P. M. C., Richard, A., Grenier, C., Chevrollier, A., Munier, M., Grimaud, L., Proux, C., Champin, T., Lelièvre, E., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202000238rrr · Cited by 42
Endothelial Cell Mechano-Metabolomic Coupling to Disease States in the Lung Microvasculature
Wu, D., & Birukov, K. G. (2019) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2019.00172 · Cited by 46
TRP Channels as Sensors of Aldehyde and Oxidative Stress
Hellenthal, K. E. M., Brabenec, L., Gross, E. R., & Wagner, N. (2021) · Biomolecules · doi:10.3390/biom11101401 · Cited by 44
Zhao, L., Zhang, C., He, L., Chen, Q., Liu, L., Kang, L., Liu, J., Luo, J., Gou, L., Qu, D. C., et al. (2022) · Diabetes · doi:10.2337/db21-0660 · Cited by 43
Ozceylan, O., & Bayındır, Z. S. (2024) · ACS Omega · doi:10.1021/acsomega.4c01774 · Cited by 43
Kim, D., Kim, K.-A., Kim, J., Kim, E.-H., & Bae, O. (2020) · Antioxidants · doi:10.3390/antiox9090820 · Cited by 40
Nannelli, G., Terzuoli, E., Giorgio, V., Donnini, S., Lupetti, P., Giachetti, A., Bernardi, P., & Ziche, M. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/9765027 · Cited by 44
Mitochondrial Dynamics: Pathogenesis and Therapeutic Targets of Vascular Diseases
Luan, Y., Ren, K., Luan, Y., Chen, X., & Yang, Y. (2021) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2021.770574 · Cited by 40
Hong, S., Shin, J., Choi, S. Y., Powers, J., Meister, B., Sayoc, J., Son, J. S., Tierney, R., Recchia, F. A., Brown, M. D., et al. (2022) · JCI Insight · doi:10.1172/jci.insight.159286 · Cited by 42
Chen, Z. B., Martin, M., Zhao, L., & Shyy, J. Y.-J. (2014) · Current Opinion in Lipidology · doi:10.1097/mol.0000000000000107 · Cited by 40
Mitophagy contributes to endothelial adaptation to simulated microgravity
Locatelli, L., Cazzaniga, A., Palma, C. D., Castiglioni, S., & Maier, J. A. M. (2019) · The FASEB Journal · doi:10.1096/fj.201901785rrr · Cited by 40
Lee, M. J., Jang, Y., Han, J., Kim, S. J., Ju, X., Lee, Y. L., Cui, J., Zhu, J., Ryu, M. J., Choi, S., et al. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x19900030 · Cited by 38
Reactive Oxygen Species-Induced TRPM2-Mediated Ca2+ Signalling in Endothelial Cells
Ding, R., Yin, Y., & Jiang, L. (2021) · Antioxidants · doi:10.3390/antiox10050718 · Cited by 39
Ramı́rez-Emiliano, J., Fajardo-Araujo, M. E., Zúñiga-Trujillo, I., Pérez‐Vázquez, V., Sandoval‐Salazar, C., & Órnelas-Vázquez, J. K. (2017) · Reproductive Biology and Endocrinology · doi:10.1186/s12958-017-0244-7 · Cited by 39
Winarto, H., Tan, M. I., Sadikin, M., & Wanandi, S. I. (2017) · Translational Oncogenomics · doi:10.1177/1177272716689818 · Cited by 38
Bosseboeuf, E., & Raimondi, C. (2020) · Cells · doi:10.3390/cells9092055 · Cited by 38
Bretón‐Romero, R., Acín‐Pérez, R., Rodríguez‐Pascual, F., Molledo, M. M., Brandes, R. P., Rial, E., Enríquez, J. A., & Lamas, S. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2014.07.003 · Cited by 39
Vacek, J. C., Behera, J., George, A. K., Kamat, P. K., Kalani, A., & Tyagi, N. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.26145 · Cited by 37
Alevriadou, B. R., Shanmughapriya, S., Patel, A., Stathopulos, P. B., & Madesh, M. (2017) · Journal of The Royal Society Interface · doi:10.1098/rsif.2017.0672 · Cited by 41
Metabolic adaptations of cells at the vascular-immune interface during atherosclerosis
Bonacina, F., Dalt, L. D., Catapano, A. L., & Norata, G. D. (2020) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2020.100918 · Cited by 37
The ketogenic diet as a therapeutic intervention strategy in mitochondrial disease
Qu, C., Keijer, J., Adjobo-Hermans, M. J. W., van de Wal, M. A. E., Schirris, T. J. J., van Karnebeek, C., Pan, Y., & Koopman, W. J. H. (2021) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2021.106050 · Cited by 37
Endothelial OCT4 is atheroprotective by preventing metabolic and phenotypic dysfunction
Shin, J., Tkachenko, S., Chaklader, M., Pletz, C., Singh, K., Bulut, G. B., Han, Y. M., Mitchell, K., Baylis, R. A., Kuzmin, A. A., et al. (2022) · Cardiovascular Research · doi:10.1093/cvr/cvac036 · Cited by 37
Tracy, E. P., Hughes, W. E., Beare, J. E., Rowe, G., Beyer, A., & LeBlanc, A. J. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0031 · Cited by 39
Why are bleeding trauma patients still dying? Towards a systems hypothesis of trauma
Dobson, G. P., Morris, J. L., & Letson, H. L. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.990903 · Cited by 34
Cathepsin E Promotes Pulmonary Emphysema via Mitochondrial Fission
Zhang, X., Shan, P., Homer, R., Zhang, Y., Petrache, I., Mannam, P., & Lee, P. J. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2014.06.017 · Cited by 36
Regulatory role of exercise-induced autophagy for sarcopenia
Liang, J., Zeng, Z., Zhang, Y., & Chen, N. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2019.110789 · Cited by 33
Perpetual change: autophagy, the endothelium, and response to vascular injury
Sachdev, U., & Lotze, M. T. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.3ru1116-484rr · Cited by 35
Hansen, N. W., Hansen, A. J., & Sams, A. G. (2017) · IUBMB Life · doi:10.1002/iub.1610 · Cited by 34
Li, C., Reif, M. M., Craige, S. M., Kant, S., & Keaney, J. F. (2016) · Nitric Oxide · doi:10.1016/j.niox.2016.03.003 · Cited by 34
Neural JNK3 regulates blood flow recovery after hindlimb ischemia in mice via an Egr1/Creb1 axis
Kant, S., Craige, S. M., Chen, K., Reif, M. M., Learnard, H., Kelly, M., Caliz, A. D., Tran, K.-V., Ramo, K., Peters, O. M., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11982-4 · Cited by 24
Mitochondrial-induced Epigenetic Modifications: From Biology to Clinical Translation
Sharma, J., Kumari, R., Bhargava, A., Tiwari, R. R., & Mishra, P. K. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666200826165735 · Cited by 32
Prdm16 Supports Arterial Flow Recovery by Maintaining Endothelial Function
Craps, S., Wauwe, J. V., Moudt, S. D., Munck, D. G. D., Leloup, A. J. A., Boeckx, B., Vervliet, T., Dheedene, W., Criem, N., Geeroms, C., et al. (2021) · Circulation Research · doi:10.1161/circresaha.120.318501 · Cited by 35
Endotheliopathy in the metabolic syndrome: Mechanisms and clinical implications
Furuta, K., Tang, X., Islam, S., Tapia, A., Chen, Z. B., & Ibrahim, S. H. (2023) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2023.108372 · Cited by 36
Fluid Mechanical Forces and Endothelial Mitochondria: A Bioengineering Perspective
Scheitlin, C. G., Nair, D. M., Crestanello, J. A., Zweier, J. L., & Alevriadou, B. R. (2014) · Cellular and Molecular Bioengineering · doi:10.1007/s12195-014-0357-4 · Cited by 34
Delivery of mitochondria-containing extracellular vesicles to the BBB for ischemic stroke therapy
Dave, K. M., Stolz, D. B., & Manickam, D. S. (2023) · Expert Opinion on Drug Delivery · doi:10.1080/17425247.2023.2279115 · Cited by 36
Gonzalez-Ibañez, A. M., Ruíz, L. M., Jensen, E. L., Echeverría, C., Romero, V., Stiles, L., Shirihai, O. S., & Elorza, Á. A. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.592035 · Cited by 32
Lee, Y., Chakraborty, S., Meininger, C. J., & Muthuchamy, M. (2018) · Microcirculation · doi:10.1111/micc.12492 · Cited by 39
Rocco, E., Grimaldi, M. C., Maino, A., Cappannoli, L., Pedicino, D., Liuzzo, G., & Biasucci, L. M. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11072055 · Cited by 31
Long Non-coding RNAs in Endothelial Biology
Weirick, T., Militello, G., & Uchida, S. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00522 · Cited by 31
Endothelial FUNDC1 Deficiency Drives Pulmonary Hypertension
Pei, Y., Ren, D., Yin, Y., Shi, J., Ai, Q., Hao, W., Luo, X., Zhang, C., Zhao, Y., Bai, C., et al. (2024) · Circulation Research · doi:10.1161/circresaha.124.325156 · Cited by 31
You, N., Liu, G., Yu, M., Chen, W., Fei, X., Sun, T., Han, M., Qin, Z., Wei, Z., & Wang, D. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2024.12.049 · Cited by 31
Wang, D., Wang, Q., Yan, G., Qiao, Y., Zhu, B., Liu, B., & Tang, C. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.9079 · Cited by 28
The Influence of Statins on the Aerobic Metabolism of Endothelial Cells
Broniarek, I., Dominiak, K., Gałgański, Ł., & Jarmuszkiewicz, W. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041485 · Cited by 29
Li, P., Xie, C., Zhong, J., Guo, Z., Guo, K., & Tu, Q. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/5589612 · Cited by 30
Song, Y., Xing, H., He, Y., Zhang, Z., Shi, G., Su, W., Liu, Y., Harrington, E. O., Sellke, F. W., & Feng, J. (2021) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/j.jtcvs.2021.06.029 · Cited by 34
Ďúranová, H., Kuželová, L., Borotová, P., Šimora, V., & Fialková, V. (2024) · Microscopy and Microanalysis · doi:10.1093/mam/ozae048 · Cited by 29
Toward Raman Subcellular Imaging of Endothelial Dysfunction
Adamczyk, A., Matuszyk, E., Radwan, B., Rocchetti, S., Chłopicki, S., & Barańśka, M. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.1c00051 · Cited by 31
Obesity Inhibits Angiogenesis Through TWIST1-SLIT2 Signaling
Hunyenyiwa, T., Hendee, K., Matus, K., Kyi, P., Mammoto, T., & Mammoto, A. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.693410 · Cited by 30
Maes, H., Olmeda, D., Soengas, M. S., & Agostinis, P. (2015) · FEBS Journal · doi:10.1111/febs.13545 · Cited by 29
Joshi, M. S., Williams, D., Horlock, D., Samarasinghe, T. D., Andrews, K. L., Jefferis, A., Berger, P. J., Chin-Dusting, J. P. F., & Kaye, D. M. (2015) · Diabetes and Vascular Disease Research · doi:10.1177/1479164114565629 · Cited by 29
Metadata
- Authors
- Kluge, M. A., Fetterman, J. L., & Vita, J. A.
- Affiliations
- Boston University (US)
- Venue
- Circulation Research
- Published
- 2013-04-12
- Volume
- 112
- Issue
- 8
- Pages
- 1171-1188
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- PMC
- PMC3700369
- OpenAlex
- W2171435588
- Cited by
- 508
- References
- 213
- Citations by year
- 2026: 25 · 2025: 44 · 2024: 49 · 2023: 34 · 2022: 60 · 2021: 52 · 2020: 49 · 2019: 33 · 2018: 37 · 2017: 37 · 2016: 25 · 2015: 25 · 2014: 34 · 2013: 4
- FWCI
- 2.76
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Circulation Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Heart, Lung, and Blood Institute (P01HL060886, R01HL102299, HL081587, P50HL083801, K12HL083781, P01HL081587, R01HL075795, T32HL007224, HL083781, R01HL083269, HL083801, HL102299, R01HL115391)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- mitochondria, endothelial cells, endothelial function, mitochondrial biogenesis, mitochondrial dynamics, mitophagy, reactive oxygen species, calcium homeostasis, regulated cell death, heme biosynthesis, vascular tone, angiogenesis, inflammation, mitochondrial-targeted therapy, cardiovascular disease
- MeSH terms
- Animals, Autophagy, Endothelium, Vascular, Homeostasis, Humans, Mitochondria, Signal Transduction, Reactive Oxygen Species, Endothelial Cells
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