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Cited 7 time in webofscience Cited 8 time in scopus
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Externalized phosphatidylinositides on apoptotic cells are eat-me signals recognized by CD14

Authors
Kim, Ok-HeeKang, Geun-HyungHur, JuneLee, JinwookJung, YunJaeHong, In-SunLee, HookeunSeo, Seung-YongLee, Dae HoLee, Cheol SoonLee, In-KyuBonner-Weir, SusanLee, JongsoonPark, Young JooKim, HyeonjinShoelson, Steven E.Oh, Byung-Chul
Issue Date
Jul-2022
Publisher
SPRINGERNATURE
Citation
CELL DEATH AND DIFFERENTIATION, v.29, no.7, pp.1423 - 1432
Journal Title
CELL DEATH AND DIFFERENTIATION
Volume
29
Number
7
Start Page
1423
End Page
1432
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/84745
DOI
10.1038/s41418-022-00931-2
ISSN
1350-9047
Abstract
Apoptotic cells are rapidly engulfed and removed by phagocytes after displaying cell surface eat-me signals. Among many phospholipids, only phosphatidylserine (PS) is known to act as an eat-me signal on apoptotic cells. Using unbiased proteomics, we identified externalized phosphatidylinositides (PIPs) as apoptotic eat-me signals recognized by CD14(+) phagocytes. Exofacial PIPs on the surfaces of early and late-apoptotic cells were observed in patches and blebs using anti-PI(3,4,5)P-3 antibody, AKT- and PLC delta PH-domains, and CD14 protein. Phagocytosis of apoptotic cells was blocked either by masking exofacial PIPs or by CD14 knockout in phagocytes. We further confirmed that exofacial PIP+ thymocytes increased dramatically after in vivo irradiation and that exofacial PIP+ cells represented more significant populations in tissues of Cd14(-/-) than WT mice, especially after induction of apoptosis. Our findings reveal exofacial PIPs to be previously unknown cell death signals recognized by CD14(+) phagocytes.
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