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  • 标题:Mouse macrophages show different requirements for phosphatidylserine receptor Tim4 in efferocytosis
  • 本地全文:下载
  • 作者:Yuichi Yanagihashi ; Katsumori Segawa ; Ryota Maeda
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2017
  • 卷号:114
  • 期号:33
  • 页码:8800-8805
  • DOI:10.1073/pnas.1705365114
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Protein S (ProS) and growth arrest-specific 6 (Gas6) bind to phosphatidylserine (PtdSer) and induce efferocytosis upon binding TAM-family receptors (Tyro3, Axl, and Mer). Here, we produced mouse ProS, Gas6, and TAM-receptor extracellular region fused to IgG fragment crystallizable region in HEK293T cells. ProS and Gas6 bound Ca2+ dependently to PtdSer ( K d 20–40 nM), Mer, and Tyro3 ( K d 15–50 nM). Gas6 bound Axl strongly ( K d < 1.0 nM), but ProS did not bind Axl. Using NIH 3T3-based cell lines expressing a single TAM receptor, we showed that TAM-mediated efferocytosis was determined by the receptor-binding ability of ProS and Gas6. Tim4 is a membrane protein that strongly binds PtdSer. Tim4 alone did not support efferocytosis, but enhanced TAM-dependent efferocytosis. Resident peritoneal macrophages, Kupffer cells, and CD169+ skin macrophages required Tim4 for TAM-stimulated efferocytosis, whereas efferocytosis by thioglycollate-elicited peritoneal macrophages or primary cultured microglia was TAM dependent, but not Tim4 dependent. These results indicate that TAM and Tim4 collaborate for efficient efferocytosis in certain macrophage populations.
  • 关键词:efferocytosis ; macrophages ; Tim4 ; apoptosis ; engulfment
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