Wnt-5A augments repopulating capacity and primitive hematopoietic development of human blood stem cells in vivo

被引:173
|
作者
Murdoch, B
Chadwick, K
Martin, M
Shojaei, F
Shah, KV
Gallacher, L
Moon, RT
Bhatia, M
机构
[1] John P Robarts Res Inst, London, ON N6A 5K8, Canada
[2] Univ Western Ontario, Dept Physiol, London, ON N6A 5K8, Canada
[3] Univ Western Ontario, Dept Microbiol & Immunol, London, ON N6A 5K8, Canada
[4] Univ Washington, Sch Med, Howard Hughes Med Inst, Dept Pharmacol, Seattle, WA 98195 USA
[5] Univ Washington, Sch Med, Howard Hughes Med Inst, Ctr Dev Biol, Seattle, WA 98195 USA
关键词
stem cell regulators;
D O I
10.1073/pnas.0130233100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Human hematopoietic stem cells are defined by their ability to repopulate multiple hematopoietic lineages in the bone marrow of transplanted recipients and therefore are functionally distinct from hematopoietic progenitors detected in vitro. Although factors capable of regulating progenitors are well established, in vivo regulators of hematopoietic repopulating function are unknown. By using a member of the vertebrate Mint family, Wnt-5A, the proliferation and differentiation of progenitors cocultured on stromal cells transduced with Wnt-5A or treated with Wnt-5A conditioned medium (CM) was unaffected. However, i.p. injection of Wnt-5A CM into mice engrafted with human repopulating cells increased multilineage reconstitution by >3-fold compared with controls. Furthermore, in vivo treatment of human repopulating cells with Wnt-5A CM produced a greater proportion of phenotypically primitive hematopoietic progeny that could be isolated and shown to possess enhanced progenitor function independent of continued Wnt-5A treatment. Our study demonstrates that Wnt-5A augments primitive hematopoietic development in vivo and represents an in vivo regulator of hematopoietic stem cell function in the human. Based on these findings, we suggest a potential role for activation of Wnt signaling in managing patients exhibiting poor hematopoietic recovery shortly after stem cell transplantation.
引用
收藏
页码:3422 / 3427
页数:6
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