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Cited by 353

The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.

SR-B1 drives endothelial cell LDL transcytosis via DOCK4 to promote atherosclerosis

Open access
Huang, Linzhang, Chambliss, Ken L., Gao, Xiaofei, Yuhanna, Ivan S., Behling-Kelly, Erica, Bergaya, Sonia, Ahmed, Mohamed, Michaely, Peter, Luby-Phelps, Kate, Darehshouri, Anza, Xu, Lin, Fisher, Edward A., Ge, Woo-Ping, Mineo, Chieko, Shaul, Philip W.·2019·Nature

Abstract

Atherosclerosis, which underlies life-threatening cardiovascular disorders such as myocardial infarction and stroke1, is initiated by passage of low-density lipoprotein (LDL) cholesterol into the artery wall and its engulfment by macrophages, which leads to foam cell formation and lesion development2,3. It is unclear how circulating LDL enters the artery wall to instigate atherosclerosis. Here we show in mice that scavenger receptor class B type 1 (SR-B1) in endothelial cells mediates the delivery of LDL into arteries and its accumulation by artery wall macrophages, thereby promoting atherosclerosis. LDL particles are colocalized with SR-B1 in endothelial cell intracellular vesicles in vivo, and transcytosis of LDL across endothelial monolayers requires its direct binding to SR-B1 and an eight-amino-acid cytoplasmic domain of the receptor that recruits the guanine nucleotide exchange factor dedicator of cytokinesis 4 (DOCK4)4. DOCK4 promotes internalization of SR-B1 and transport of LDL by coupling the binding of LDL to SR-B1 with activation of RAC1. The expression of SR-B1 and DOCK4 is increased in atherosclerosis-prone regions of the mouse aorta before lesion formation, and in human atherosclerotic arteries when compared with normal arteries. These findings challenge the long-held concept that atherogenesis involves passive movement of LDL across a compromised endothelial barrier. Interventions that inhibit the endothelial delivery of LDL into artery walls may represent a new therapeutic category in the battle against cardiovascular disease. The SR-B1 receptor partners with DOCK4 and RAC1 to drive the uptake and transcytosis of LDL in endothelial cells, thereby promoting atherosclerosis in mice.

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Metadata

Authors
Huang, L., Chambliss, K. L., Gao, X., Yuhanna, I. S., Behling-Kelly, E., Bergaya, S., Ahmed, M., Michaely, P., Luby-Phelps, K., Darehshouri, A., Xu, L., Fisher, E. A., Ge, W.-P., Mineo, C., & Shaul, P. W.
Venue
Nature
Published
2019-04-24
Volume
569
Issue
7757
Pages
565-569
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W2942368772
Cited by
353
References
54
FWCI
12.18
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: SR-B1 drives endothelial cell LDL transcytosis via DOCK4 to promote atherosclerosis. https://app.cochat.ai/papers/10.1038/s41586-019-1140-4
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Huang, L., Chambliss, K. L., Gao, X., Yuhanna, I. S., Behling-Kelly, E., Bergaya, S., Ahmed, M., Michaely, P., Luby-Phelps, K., Darehshouri, A., Xu, L., Fisher, E. A., Ge, W.-P., Mineo, C., & Shaul, P. W. (2019). SR-B1 drives endothelial cell LDL transcytosis via DOCK4 to promote atherosclerosis. Nature. https://doi.org/10.1038/s41586-019-1140-4

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.