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Sterol Regulatory Element Binding Protein 2 Activation of NLRP3 Inflammasome in Endothelium Mediates Hemodynamic-Induced Atherosclerosis Susceptibility
Open accessAbstract
Background—: The molecular basis for the focal nature of atherosclerotic lesions is poorly understood. Here, we explored whether disturbed flow patterns activate an innate immune response to form the NLRP3 inflammasome scaffold in vascular endothelial cells via sterol regulatory element binding protein 2 (SREBP2). Methods and Results—: Oscillatory flow activates SREBP2 and induces NLRP3 inflammasome in endothelial cells. The underlying mechanisms involve SREBP2 transactivating NADPH oxidase 2 and NLRP3. Consistently, SREBP2, NADPH oxidase 2, and NLRP3 levels were elevated in atheroprone areas of mouse aortas, suggesting that the SREBP2-activated NLRP3 inflammasome causes functionally disturbed endothelium with increased inflammation. Mimicking the effect of atheroprone flow, endothelial cell–specific overexpression of the activated form of SREBP2 synergized with hyperlipidemia to increase atherosclerosis in the atheroresistant areas of mouse aortas. Conclusions—: Atheroprone flow induces NLRP3 inflammasome in endothelium through SREBP2 activation. This increased innate immunity in endothelium synergizes with hyperlipidemia to cause topographical distribution of atherosclerotic lesions.
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“Moreover, recent studies have demonstrated that sterol regulatory element binding protein 2 activation of NLRP3 inflammasome in endothelium mediates hemodynamic‐induced AS susceptibility,11”
From Trimethylamine‐N‐Oxide Induces Vascular Inflammation by Activating the NLRP3 Inflammasome Through the SIRT3‐SOD2‐mtROS Signaling Pathway (2017) · cites this paper as [11]
In the citing paper
“Xiao et al11 additionally reported that atheroprone flow induces the NLRP3 inflammasome in endothelium through serol regulatory element binding protein 2 activation.”
From Trimethylamine‐N‐Oxide Induces Vascular Inflammation by Activating the NLRP3 Inflammasome Through the SIRT3‐SOD2‐mtROS Signaling Pathway (2017) · cites this paper as [11]
In the citing paper
“This increased innate immunity in endothelium synergizes with hyperlipidemia to cause topographical distribution of atherosclerotic lesions.11”
From Trimethylamine‐N‐Oxide Induces Vascular Inflammation by Activating the NLRP3 Inflammasome Through the SIRT3‐SOD2‐mtROS Signaling Pathway (2017) · cites this paper as [11]
In the citing paper
“These results clearly indicate that the NLRP3 inflammasome plays a key role in the pathogenesis of vascular inflammation, thereby contributing to AS development.”
From Trimethylamine‐N‐Oxide Induces Vascular Inflammation by Activating the NLRP3 Inflammasome Through the SIRT3‐SOD2‐mtROS Signaling Pathway (2017) · cites this paper as [11]
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Citations
Cites
Atherosclerosis--an inflammatory disease
Ross, R. (1999) · New England Journal of Medicine · doi:10.1056/nejm199901143400207 · Cited by 21,725
NLRP3 inflammasomes are required for atherogenesis and activated by cholesterol crystals
Duewell, P., Kono, H., Rayner, K. J., Sirois, C. M., Vladimer, G., Bauernfeind, F. G., Abela, G. S., Franchi, L., Nuñez, G., Schnurr, M., et al. (2010) · Nature · doi:10.1038/nature08938 · Cited by 4,026
Thioredoxin-interacting protein links oxidative stress to inflammasome activation
Zhou, R., Tardivel, A., Thorens, B., Choi, I., & Tschopp, J. (2010) · Nature Immunology · doi:10.1038/ni.1831 · Cited by 2,708
Innate Immune Activation Through Nalp3 Inflammasome Sensing of Asbestos and Silica
Dostert, C., Pétrilli, V., Van Bruggen, R., Steele, C., Mossman, B. T., & Tschopp, J. (2008) · Science · doi:10.1126/science.1156995 · Cited by 2,658
Chiu, J.-J., & Chien, S. (2011) · Physiological Reviews · doi:10.1152/physrev.00047.2009 · Cited by 2,280
Li, Y., Xu, S., Mihaylova, M. M., Zheng, B., Hou, X., Jiang, B., Park, O., Luo, Z., Lefai, É., Shyy, J. Y.-J., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.03.009 · Cited by 1,840
Self-citationMiR-33 Contributes to the Regulation of Cholesterol Homeostasis
Rayner, K. J., Suárez, Y., Dávalos, A., Parathath, S., Fitzgerald, M. L., Tamehiro, N., Fisher, E. A., Moore, K. J., & Fernández-Hernando, C. (2010) · Science · doi:10.1126/science.1189862 · Cited by 1,260
Hemodynamic shear stress and the endothelium in cardiovascular pathophysiology
Davies, P. F. (2008) · Nature Clinical Practice Cardiovascular Medicine · doi:10.1038/ncpcardio1397 · Cited by 1,216
Rajamäki, K., Lappalainen, J., Öörni, K., Välimäki, E., Matikainen, S., Kovanen, P. T., & Eklund, K. K. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011765 · Cited by 1,039
MicroRNA-33 and the SREBP Host Genes Cooperate to Control Cholesterol Homeostasis
Najafi-Shoushtari, S. H., Kristo, F., Li, Y., Shioda, T., Cohen, D. E., Gerszten, R. E., & Näär, A. M. (2010) · Science · doi:10.1126/science.1189123 · Cited by 957 · cited 2×
“In macrophages, the SREBP2-coinduced miR-33a targets ABCA1, which impairs reverse cholesterol transport.(5,6) An antigomir against miR-33 decreases atherosclerosis in LDL receptor–null mice, with a concomitant increase in the level of high-density lipoprotein.”
Background
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Ridker, P. M., Everett, B. M., Thuren, T., MacFadyen, J. G., Chang, W. H., Ballantyne, C., Fonseca, F., Nicolau, J., Koenig, W., Anker, S. D., et al. (2017) · New England Journal of Medicine · doi:10.1056/nejmoa1707914 · Cited by 9,482
Cholesterol, inflammation and innate immunity.
Tall, A. R., & Yvan-Charvet, L. (2015) · Nature Reviews Immunology · doi:10.1038/nri3793 · Cited by 1,479
Ridker, P. M. (2016) · Circulation Research · doi:10.1161/circresaha.115.306656 · Cited by 1,002
Redox Regulation of NLRP3 Inflammasomes: ROS as Trigger or Effector?
Abais, J. M., Xia, M., Zhang, Y., Boini, K. M., & Li, P. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2014.5994 · Cited by 936
Interleukin-1 Beta as a Target for Atherosclerosis Therapy
Libby, P. (2017) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2017.09.028 · Cited by 651
Chen, M., Zhu, X., Ran, L., Lang, H., Yi, L., & Mi, M. (2017) · Journal of the American Heart Association · doi:10.1161/jaha.117.006347 · Cited by 600
Endothelial fluid shear stress sensing in vascular health and disease
Baeyens, N., Bandyopadhyay, C., Coon, B. G., Yun, S., & Schwartz, M. A. (2016) · Journal of Clinical Investigation · doi:10.1172/jci83083 · Cited by 592
Inflammatory Mechanisms Contributing to Endothelial Dysfunction
Theofilis, P., Sagris, Μ., Oikonomou, E. K., Antonopoulos, A. S., Siasos, G., Tsioufis, C. P., & Tousoulis, D. (2021) · Biomedicines · doi:10.3390/biomedicines9070781 · Cited by 574
Shear Stress–Initiated Signaling and Its Regulation of Endothelial Function
Zhou, J., Li, Y.-S. J., & Chien, S. (2014) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.114.303422 · Cited by 594
Anti-inflammatory therapies for cardiovascular disease
Ridker, P. M., & Lüscher, T. F. (2014) · European Heart Journal · doi:10.1093/eurheartj/ehu203 · Cited by 568
Biomechanical factors in atherosclerosis: mechanisms and clinical implications
Kwak, B. R., Bäck, M., Bochaton‐Piallat, M., Caligiuri, G., Daemen, M. J. A. P., Davies, P. F., Hoefer, I. E., Holvoet, P., Jo, H., Krams, R., et al. (2014) · European Heart Journal · doi:10.1093/eurheartj/ehu353 · Cited by 515
Inflammation in atherosclerosis: pathophysiology and mechanisms
Ajoolabady, A., Praticò, D., Lin, L., Mantzoros, C. S., Bahijri, S., Tuomilehto, J. O., & Ren, J. T. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-07166-8 · Cited by 532
Ridker, P. M. (2016) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2015.11.037 · Cited by 414
Arterial ageing: from endothelial dysfunction to vascular calcification
Tesauro, M., Mauriello, A., Rovella, V., Annicchiarico‐Petruzzelli, M., Cardillo, C., Melino, G., & Daniele, N. D. (2017) · Journal of Internal Medicine · doi:10.1111/joim.12605 · Cited by 332
Pyroptosis, metabolism, and tumor immune microenvironment
Du, T., Gao, J., Li, P., Wang, Y., Qi, Q., Liu, X., Li, J., Wang, C., & Du, L. (2021) · Clinical and Translational Medicine · doi:10.1002/ctm2.492 · Cited by 335
Endothelial NADPH oxidases: which NOX to target in vascular disease?
Drummond, G. R., & Sobey, C. G. (2014) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2014.06.012 · Cited by 315
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Shao, Y., Saredy, J., Yang, W. Y., Sun, Y., Lu, Y., Saaoud, F., Drummer, C., Johnson, C., Xu, K., Jiang, X., et al. (2020) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.120.314330 · Cited by 302
NLRP3 at the interface of metabolism and inflammation
Haneklaus, M., & O'Neill, L. A. J. (2015) · Immunological Reviews · doi:10.1111/imr.12285 · Cited by 296
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Patel, M. N., Carroll, R. G., Galván-Peña, S., Mills, E. L., Olden, R., Triantafilou, M., Wolf, A. I., Bryant, C. E., Triantafilou, K., & Masters, S. L. (2017) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2016.12.007 · Cited by 241
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Antonopoulos, C. H., Russo, H. M., Sanadi, C. E. E., Martin, B. N., Li, X., Kaiser, W. J., Mocarski, E. S., & Dubyak, G. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.652321 · Cited by 232
Sharma, A., Tate, M., Mathew, G., Vince, J. E., Ritchie, R. H., & de Haan, J. B. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00114 · Cited by 221
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Yin, Y., Li, X., Sha, X., Xi, H., Li, Y., Shao, Y., Mai, J., Virtue, A. T., Lopez‐Pastrana, J., Meng, S., et al. (2015) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.115.305282 · Cited by 207
NLRP3 inflammasome pathways in atherosclerosis
Baldrighi, M., Mallat, Z., & Li, X. (2017) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2017.10.027 · Cited by 204
The arterial microenvironment: the where and why of atherosclerosis
Yurdagul, A., Finney, A. C., Woolard, M. D., & Orr, A. W. (2016) · Biochemical Journal · doi:10.1042/bj20150844 · Cited by 185
Updated insights into the molecular networks for NLRP3 inflammasome activation
Paik, S., Kim, J. K., Shin, H. J., Park, E., Kim, I. S., & Jo, E. (2025) · Cellular and Molecular Immunology · doi:10.1038/s41423-025-01284-9 · Cited by 222
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Miguel, V., Shaw, I., & Kramann, R. (2024) · Nature Reviews Nephrology · doi:10.1038/s41581-024-00889-z · Cited by 216
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Zhuang, T., Liu, J., Chen, X., Zhang, L., Pi, J., Sun, H., Li, L., Bauer, R. C., Wang, H., Yu, Z., et al. (2019) · Circulation Research · doi:10.1161/circresaha.118.314402 · Cited by 188
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Xu, C., Wan, X., Xu, L., Weng, H., Yan, M., Miao, M., Sun, Y., Xu, G.-Y., Dooley, S., Li, Y., et al. (2015) · Journal of Hepatology · doi:10.1016/j.jhep.2015.01.019 · Cited by 186
Wu, D., Huang, R., Hamanaka, R. B., Krause, M., Oh, M., Kuo, C., Niğdelioğlu, R., Meliton, A. Y., Witt, L. J., Dai, G., et al. (2017) · eLife · doi:10.7554/elife.25217 · Cited by 184
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Fairweather, D. (2014) · Clinical Medicine Insights Cardiology · doi:10.4137/cmc.s17068 · Cited by 172
Botts, S. R., Fish, J. E., & Howe, K. L. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.787541 · Cited by 181
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He, X., Fan, X., Bai, B., Lu, N., Zhang, S., & Zhang, L. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105447 · Cited by 174
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Head, T., Daunert, S., & Goldschmidt‐Clermont, P. J. (2017) · Frontiers in Genetics · doi:10.3389/fgene.2017.00216 · Cited by 172
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Williams, J. W., Huang, L.-H., & Randolph, G. J. (2019) · Immunity · doi:10.1016/j.immuni.2019.03.007 · Cited by 168
Meng, Q., Li, Y., Ji, T., Chao, Y., Li, J., Fu, Y., Wang, S., Chen, Q., Chen, W., Huang, F., et al. (2020) · Journal of Advanced Research · doi:10.1016/j.jare.2020.08.010 · Cited by 159
RetractedChen, Z. B., Wen, L., Martin, M., Hsu, C., Fang, L., Lin, F.-M., Lin, T.-Y., Geary, M. J., Geary, G. G., Zhao, Y., et al. (2014) · Circulation · doi:10.1161/circulationaha.114.013675 · Cited by 158
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Dumas, S. J., Meta, E., Borri, M., Luo, Y., Li, X., Rabelink, T. J., & Carmeliet, P. (2021) · Nature Reviews Nephrology · doi:10.1038/s41581-021-00411-9 · Cited by 165
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Jin, Y. H., & Fu, J. (2019) · Journal of the American Heart Association · doi:10.1161/jaha.119.012219 · Cited by 153
Role of vascular smooth muscle cell in the inflammation of atherosclerosis
Lim, S., & Park, S. (2014) · BMB Reports · doi:10.5483/bmbrep.2014.47.1.285 · Cited by 149
Mechanisms of NLRP3 priming in inflammaging and age related diseases
Gritsenko, A., Green, J., Brough, D., & López‐Castejón, G. (2020) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2020.08.003 · Cited by 146
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Miller, Y. I., & Shyy, J. Y.-J. (2016) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2016.11.002 · Cited by 141
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Anderson, F. L., Biggs, K. E., Rankin, B. E., & Havrda, M. C. (2022) · Translational research · doi:10.1016/j.trsl.2022.08.006 · Cited by 154
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Ji, N., Qi, Z., Wang, Y., Yang, X., Yan, Z., Li, M., Ge, Q., & Zhang, J. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s308177 · Cited by 135
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He, J., Zhang, G., Pang, Q., Yu, C., Xiong, J., Zhu, J., & Chen, F. (2017) · FEBS Journal · doi:10.1111/febs.14055 · Cited by 124
Penna, C. R. R., & Pagliaro, P. (2025) · Antioxidants · doi:10.3390/antiox14030256 · Cited by 142
Li, Z., Martin, M., Zhang, J., Huang, H., Bai, L., Zhang, J., Kang, J., He, M., Li, J., Maurya, M. R., et al. (2017) · Circulation · doi:10.1161/circulationaha.117.027462 · Cited by 124
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Oikonomou, E. K., Leopoulou, M., Theofilis, P., Antonopoulos, A. S., Siasos, G., Latsios, G., Mystakidi, V. C., Antoniades, C. A., & Tousoulis, D. (2020) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2020.07.027 · Cited by 117
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Sun, X., Fu, Y., Gu, M., Zhang, L., Li, D., Li, H., Chien, S., Shyy, J. Y.-J., & Zhu, Y. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1524523113 · Cited by 109
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Self-citationSchunk, S. J., Kleber, M. E., März, W., Pang, S., Zewinger, S., Triem, S., Ege, P., Reichert, M., Krawczyk, M. J., Weber, S. N., et al. (2021) · European Heart Journal · doi:10.1093/eurheartj/ehab107 · Cited by 100
Wang, S., Xie, X., Lei, T., Zhang, K., Lai, B., Zhang, Z., Guan, Y., Mao, G., Xiao, L., & Wang, N. (2017) · Molecular Pharmacology · doi:10.1124/mol.116.108100 · Cited by 93
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Wan, Z., Fan, Y., Liu, X., Xue, J., Han, Z., Zhu, C., & Wang, X. (2019) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s222053 · Cited by 93
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Tsai, S., Huang, P., Hsu, Y., Peng, Y., Lee, C., Wang, J., Chen, J., & Lin, S. (2016) · Scientific Reports · doi:10.1038/srep28612 · Cited by 89
Self-citationBai, R., Lang, Y., Shao, J., Deng, Y., Refuhati, R., & Cui, L. (2021) · ASN NEURO · doi:10.1177/17590914211018100 · Cited by 86
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Self-citationShao, Y., Saredy, J., Xu, K., Sun, Y., Saaoud, F., Drummer, C., Lu, Y., Luo, J. J., Lopez‐Pastrana, J., Choi, E. T., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.653110 · Cited by 75
He, M., Huang, T.-S., Li, S., Hong, H.-C., Chen, Z. B., Martin, M., Zhou, X., Huang, H., Su, S., Zhang, J., et al. (2019) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.118.312301 · Cited by 70
Self-citationMahmoudi, M., Farghadan, A., McConnell, D. R., Barker, A. J., Wentzel, J. J., Budoff, M. J., & Arzani, A. (2020) · Journal of Biomechanical Engineering · doi:10.1115/1.4049026 · Cited by 71
Endothelial cell dysfunction in cardiac disease: driver or consequence?
Allbritton‐King, J. D., & García‐Cardeña, G. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1278166 · Cited by 69
Hadri, K. E., Smith, R., Duplus, E., & Amri, C. E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010077 · Cited by 71
Emerging Roles of Mitochondria ROS in Atherosclerotic Lesions: Causation or Association?
Wang, Y., & Tabas, I. A. (2014) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat.23929 · Cited by 71
Inflammatory Mediators of Platelet Activation: Focus on Atherosclerosis and COVID-19
Theofilis, P., Sagris, Μ., Antonopoulos, A. S., Oikonomou, E. K., Tsioufis, C. P., & Tousoulis, D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011170 · Cited by 74
Kotlyarov, S. N., & Котлярова, А. А. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031308 · Cited by 67
The NLRP3 Inflammasome: An Important Driver of Neuroinflammation in Hemorrhagic Stroke
Shao-jun, Y., Shao, G., Chen, J., & Gong, J. (2017) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-017-0526-9 · Cited by 68
Self-citationCoulon, P.-G. A., Dhanushkodi, N. R., Prakash, S., Srivastava, R., Roy, S., Alomari, N. I., Nguyen, A., Warsi, W. R., Ye, C., Carlos-Cruz, E. A., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01631 · Cited by 66
A Revised Hemodynamic Theory of Age-Related Macular Degeneration
Gelfand, B. D., & Ambati, J. (2016) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2016.06.009 · Cited by 65
Chen, L., Hou, X., Zhang, M., Zheng, Y., Zheng, X., Yang, Q., Li, J., Gu, N., Zhang, M., Sun, Y., et al. (2019) · Molecular Immunology · doi:10.1016/j.molimm.2019.10.027 · Cited by 65
Berg, M., Polyzos, K. A., Agardh, H. E., Baumgartner, R., Forteza, M. J., Kareinen, I., Gisterå, A., Böttcher, G., Hurt‐Camejo, E., Hansson, G. K., et al. (2019) · Cardiovascular Research · doi:10.1093/cvr/cvz258 · Cited by 65
Celastrol ameliorates inflammation through inhibition of NLRP3 inflammasome activation
Yu, X., Zhao, Q., Zhang, X., Zhang, H., Liu, Y., Wu, X., Li, M., Li, X., Zhang, J., Ruan, X., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.18619 · Cited by 60
McRae, S., Iqbal, J., Sarkar-Dutta, M., Lane, S., Nagaraj, A., Ali, N., & Waris, G. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.694059 · Cited by 58
RetractedComputational modelling of atherosclerosis
Parton, A., McGilligan, V., O’Kane, M., Baldrick, F. R., & Watterson, S. (2015) · Briefings in Bioinformatics · doi:10.1093/bib/bbv081 · Cited by 60
Synergistic effects of colchicine combined with atorvastatin in rats with hyperlipidemia
Huang, C., Cen, C., Wang, C., Zhan, H., & Ding, X. (2014) · Lipids in Health and Disease · doi:10.1186/1476-511x-13-67 · Cited by 56
Liu, Y., Wei, W., Wang, Y., Wan, C., Bai, Y., Sun, X., Ma, J., & Zheng, F. (2019) · Inflammation Research · doi:10.1007/s00011-019-01244-w · Cited by 56
Metadata
- Authors
- Xiao, H., Lu, M., Lin, T. Y., Chen, Z., Chen, G., Wang, W.-C., Marin, T., Shentu, T.-P., Wen, L., Gongol, B., Sun, W., Liang, X., Chen, J., Huang, H.-D., Pedra, J. H. F., Johnson, D. A., & Shyy, J. Y.-J.
- Affiliations
- University of California, Riverside (US)
- ORCID
- Venue
- Circulation
- Published
- 2013-08-06
- Volume
- 128
- Issue
- 6
- Pages
- 632-642
- ISSN
- 0009-7322 (ISSN-L)
- 1524-4539
- PMC
- PMC3798034
- OpenAlex
- W2022621797
- Cited by
- 257
- References
- 47
- Citations by year
- 2026: 14 · 2025: 15 · 2024: 14 · 2023: 15 · 2022: 22 · 2021: 32 · 2020: 18 · 2019: 23 · 2018: 15 · 2017: 19 · 2016: 25 · 2015: 17 · 2014: 25 · 2013: 2
- FWCI
- 12.71
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Circulation (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Natural Science Foundation of China (81270349)
- National Science Council (NSC 101-2311-B-009-003-MY3, NSC 100-2627-B-009-002, NSC 101-2911-I-009-101)
- National Institutes of Health
- University of California, San Diego
- National Heart, Lung, and Blood Institute (R01HL105318, R01HL089940, HL89940, HL105318)
- National Institute of Allergy and Infectious Diseases (R01AI093653)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Cholesterol and Lipid Metabolism
- Keywords
- SREBP2, NLRP3 inflammasome, endothelial cells, oscillatory flow, flow disturbance, atherosclerosis, hemodynamics, NADPH oxidase 2, innate immunity, hyperlipidemia
- MeSH terms
- NLR Family, Pyrin Domain-Containing 3 Protein, NADPH Oxidase 2, Animals, Apolipoproteins E, Carrier Proteins, Hemodynamics, Humans, Immunity, Innate, Male, Membrane Glycoproteins, Mice, Transgenic, Stress, Mechanical, Vasculitis, NADPH Oxidases, RNA, Small Interfering, MicroRNAs, Endothelial Cells, Atherosclerosis, Mice, Sterol Regulatory Element Binding Protein 2, Inflammasomes, Human Umbilical Vein Endothelial Cells
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