Fetal and adult hematopoietic stem cells require β1 integrin function for colonizing fetal liver, spleen, and bone marrow

被引:275
作者
Potocnik, AJ
Brakebusch, C
Fässler, R
机构
[1] Max Planck Inst Immunbiol, D-79108 Freiburg, Germany
[2] Basel Inst Immunol, CH-4005 Basel, Switzerland
[3] Univ Lund, Dept Expt Pathol, S-22185 Lund, Sweden
基金
新加坡国家研究基金会;
关键词
D O I
10.1016/S1074-7613(00)80216-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Homing of hematopoietic stem cells (HSCs) into hematopoietic organs is a prerequisite for the establishment of hematopoiesis during embryogenesis and after bone marrow transplantation. We show that beta 1 integrin-deficient HSCs from the para-aortic splanchnopleura and the fetal blood had hematolymphoid differentiation potential in vitro and in fetal organ cultures but were unable to seed fetal and adult hematopoietic tissues. Adult beta 1 integrin null HSCs isolated from mice carrying loxP-tagged beta 1 integrin alleles and ablated for beta 1 integrin expression by retroviral cre transduction failed to engraft irradiated recipient mice. Moreover, absence of beta 1 integrin resulted in sequestration of HSCs in the circulation and their reduced adhesion to endothelioma cells. These findings define beta 1 integrin as an essential adhesion receptor for the homing of HSCs.
引用
收藏
页码:653 / 663
页数:11
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