Monocytes-macrophages that express α-smooth muscle actin preserve primitive hematopoietic cells in the bone marrow

被引:168
作者
Ludin, Aya [1 ]
Itkin, Tomer [1 ]
Gur-Cohen, Shiri [1 ]
Mildner, Alexander [1 ]
Shezen, Elias [1 ]
Golan, Karin [1 ]
Kollet, Orit [1 ]
Kalinkovich, Alexander [1 ]
Porat, Ziv [2 ]
D'Uva, Gabriele [1 ]
Schajnovitz, Amir [1 ]
Voronov, Elena [3 ]
Brenner, David A. [4 ]
Apte, Ron N. [3 ]
Jung, Steffen [1 ]
Lapidot, Tsvee [1 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Flow Cytometry Unit, Dept Biol Serv, IL-76100 Rehovot, Israel
[3] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Microbiol & Immunol, IL-84105 Beer Sheva, Israel
[4] Univ Calif San Diego, Dept Med, San Diego, CA 92103 USA
关键词
PROGENITOR CELLS; STEM-CELLS; STROMAL CELLS; PROSTAGLANDIN-E2; MYELOPOIESIS; MOBILIZATION; MODULATION; INHIBITION; NICHES;
D O I
10.1038/ni.2408
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hematopoietic stem and progenitor cells (HSPCs) are regulated by various bone marrow stromal cell types. Here we identified rare activated bone marrow monocytes and macrophages with high expression of a-smooth muscle actin (alpha-SMA) and the cyclooxygenase COX-2 that were adjacent to primitive HSPCs. These myeloid cells resisted radiation-induced cell death and further upregulated COX-2 expression under stress conditions. COX-2-derived prostaglandin E-2 (PGE(2)) prevented HSPC exhaustion by limiting the production of reactive oxygen species (ROS) via inhibition of the kinase Akt and higher stromal-cell expression of the chemokine CXCL12, which is essential for stem-cell quiescence. Our study identifies a previously unknown subset of alpha-SMA(+) activated monocytes and macrophages that maintain HSPCs and protect them from exhaustion during alarm situations.
引用
收藏
页码:1072 / 1082
页数:11
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