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Cited by 268

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

A Role of RIP3-Mediated Macrophage Necrosis in Atherosclerosis Development

Open access
Lin, Juan, Li, Hanjie, Yang, Min, Ren, Junming, Huang, Zhe, Han, Felicia, Huang, Jian, Ma, Jianhui, Zhang, Duanwu, Zhang, Zhirong, Wu, Jianfeng, Huang, Deli, Qiao, Muzhen, Jin, Guanghui, Wu, Qiao, Huang, Yinghui, Du, Jie, Han, Jiahuai·2013·Cell Reports

Abstract

Necrotic death of macrophages has long been known to be present in atherosclerotic lesions but has not been studied. We examined the role of receptor interacting protein (RIP) 3, a mediator of necrotic cell death, in atherosclerosis and found that RIP3(-/-);Ldlr(-/-) mice were no different from RIP3(+/+);Ldlr(-/-) mice in early atherosclerosis but had significant reduction in advanced atherosclerotic lesions. Similar results were observed in Apoe(-/-) background mice. Bone marrow transplantation revealed that loss of RIP3 expression from bone-marrow-derived cells is responsible for the reduced disease progression. While no difference was found in apoptosis between RIP3(-/-);Ldlr(-/-) and RIP3(+/+);Ldlr(-/-) mice, electron microscopy revealed a significant reduction of macrophage primary necrosis in the advanced lesions of RIP3(-/-) mice. In vitro cellular studies showed that RIP3 deletion had no effect on oxidized low-density lipoprotein (LDL)-induced macrophage apoptosis, but prevented macrophage primary necrosis occurring in response to oxidized LDL under caspase inhibition or RIP3 overexpression conditions. RIP3-dependent necrosis is not postapoptotic, and the increased primary necrosis in advanced atherosclerotic lesions most likely resulted from the increase of RIP3 expression. Our data demonstrate that primary necrosis of macrophages is proatherogenic during advanced atherosclerosis development.

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Crossref · 10.1016/j.celrep.2012.12.012

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Metadata

Authors
Lin, J., Li, H., Yang, M., Ren, J., Huang, Z., Han, F., Huang, J., Ma, J., Zhang, D., Zhang, Z., Wu, J., Huang, D., Qiao, M., Jin, G., Wu, Q., Huang, Y., Du, J., & Han, J.
Venue
Cell Reports
Publisher
Elsevier BV
Published
2013-01
Volume
3
Issue
1
Pages
200-210
ISSN
2211-1247 (ISSN-L)
OpenAlex
W2090263751
Cited by
268
References
9
FWCI
13.06
Type
journal article
Language
en
Open access
gold

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