Hematopoietic stem cells are uniquely selective in their migratory response to chemokines

被引:383
作者
Wright, DE
Bowman, EP
Wagers, AJ
Butcher, EC
Weissman, IL
机构
[1] Stanford Univ, Sch Med, Dept Pathol 5324, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Lab Immunol & Vasc Biol, Dept Pathol, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Ctr Digest Dis, Dept Med, Stanford, CA 94305 USA
[5] Ctr Mol Biol & Med, Vet Affairs Palo Alto Hlth Care Syst, Stanford, CA 94305 USA
[6] DNAX Res Inst Mol & Cellular Biol Inc, Dept Immunol, Palo Alto, CA 94304 USA
关键词
chemokines; chemokine receptors; chemotaxis; mobilization; bone marrow;
D O I
10.1084/jem.20011284
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although hematopoietic stern cell (HSC) migration into and out of sites of active hematopoiesis is poorly understood, it is a critical process that underlies modern clinical stern cell transplantation and may be important for normal hematopoietic homeostasis. Given the established roles of chemotactic cytokine (chemokine)-directed migration of other leukocyte subsets, the migration of murine HSC to a large panel of CC and CXC chemokines was investigated. HSC migrated only in response to stromal derived factor-la, the ligand for the CXC chemokine receptor 4 (CXCR4). CXCR4 expression by HSC was confirmed by reverse transcription polymerase chain reaction analysis. Surprisingly, HSC also expressed mRNA for CCP3 and CCR9, although they failed to migrate to the ligands for these receptors. The sharply restricted chemotactic responsiveness of HSC is unique among leukocytes and may be necessary for the specific homing of circulating HSC to bone marrow, as well as for the maintenance of HSC in hematopoietic microenvironments.
引用
收藏
页码:1145 / 1154
页数:10
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