Abstract
AbstractApoptotic 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)P3antibody, AKT- and PLCδ 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 ofCd14−/−than WT mice, especially after induction of apoptosis. Our findings reveal exofacial PIPs to be previously unknown cell death signals recognized by CD14+phagocytes.
Funder
National Research Foundation of Korea
Joslin Diabetes Center
U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases
National Research Foundation
Ministry of Health and Welfare
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology
Cited by
16 articles.
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