A distinct subset of podoplanin (gp38) expressing F4/80+ macrophages mediate phagocytosis and are induced following zymosan peritonitis

被引:37
作者
Hou, Tie Zheng
Bystrom, Jonas [2 ]
Sherlock, Jonathan P.
Qureshi, Omar
Parnell, Sonia M.
Anderson, Graham
Gilroy, Derek W. [2 ]
Buckley, Christopher D. [1 ]
机构
[1] Univ Birmingham, Coll Med & Dent Sci, Sch Immun & Infect, Rheumatol Res Grp,MRC,Ctr Immune Regulat, Birmingham B15 2TT, W Midlands, England
[2] UCL, Ctr Clin Pharmacol & Therapeut, Div Med, London, England
基金
英国惠康基金;
关键词
Podoplanin; Spleen; Fibroblastic macrophage; Phagocytosis; Resolution; Inflammation; CELLS; NEOANGIOGENESIS; INFLAMMATION; RESOLUTION;
D O I
10.1016/j.febslet.2010.07.053
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macrophages are important tissue resident cells that regulate the dynamics of inflammation. However, they are strikingly heterogeneous. During studies looking at podoplanin (gp38) expression on stromal cells in the murine spleen and peritoneal cavity we unexpectedly discovered that podoplanin was expressed on a subset of F4/80(+) macrophages; a subset which we have termed fibroblastic macrophages (FM). These cells function as phagocytes in vitro as measured by bead mediated phagocytosis assays. FM also exist at high frequency in the peritoneal cavity and in zymosan induced peritonitis in vivo. These FM represent a unique subgroup of F4/80(+) macrophages and their presence in the inflamed peritoneum suggests that they play a role in zymosan induced peritonitis. (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3955 / 3961
页数:7
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