Wnt signaling regulates hemopoiesis through stromal cells

被引:68
作者
Yamane, T
Kunisada, T
Tsukamoto, H
Yamazaki, H
Niwa, H
Takada, S
Hayashi, SI
机构
[1] Tottori Univ, Fac Med, Sch Life Sci, Dept Immunol, Yonago, Tottori 6838503, Japan
[2] RIKEN, Ctr Dev Biol, Lab Pluripotent Cell Studies, Kobe, Hyogo, Japan
[3] Kyoto Univ, Grad Sch Sci, Ctr Mol & Dev Biol, Kyoto, Japan
关键词
D O I
10.4049/jimmunol.167.2.765
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hemopoietic cells develop in a complex milieu that is made up of diverse components, including stromal cells. Wnt genes, which are known to regulate the fate of the cells in a variety of tissues, are expressed in hemopoietic organs. However, their roles in hemopoiesis are not well characterized. In this study, we examined the roles of Wnt proteins in hemopoiesis using conditioned medium containing Wnt-3a. This conditioned medium dramatically reduced the production of B lineage cells and myeloid lineage cells, except for macrophages in the long-term bone marrow cultures grown on stromal cells, although the sensitivity to the conditioned medium differed, depending on the hemopoietic lineage. In contrast, the same conditioned medium did not affect the generation of B lineage or myeloid lineage cells in stromal cell-free conditions. These results suggested that Wnt proteins exert their effects through stromal cells. Indeed, these effects were mimicked by the expression of a stabilized form of beta -catenin in stromal cells. In this study, we demonstrated that Wnt signaling regulates hemopoiesis through stromal cells with selectivity and different degrees of the effect, depending on the hemopoietic lineage in the hemopoietic microenvironment.
引用
收藏
页码:765 / 772
页数:8
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