Fetal anemia and apoptosis of red cell progenitors in Stat5a-/-5b-/- mice:: A direct role for Stat5 in Bcl-XL induction

被引:595
作者
Socolovsky, M
Fallon, AEJ
Wang, S
Brugnara, C
Lodish, HF
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02138 USA
[3] Harvard Univ, Sch Med, Childrens Hosp, Dept Lab Med, Boston, MA 02115 USA
关键词
D O I
10.1016/S0092-8674(00)81013-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The erythropoietin receptor (EpoR) is essential for production of red blood cells; a principal function of EpoR is to rescue committed erythroid progenitors from apoptosis. Stat5 is rapidly activated following EpoR stimulation, but its function in erythropoiesis has been unclear since adult Stat5a(-/-)5b(-/-) mice have normal steady-state hematocrit. Here we show that Stat5 is essential for the high erythropoietic rate during fetal development. Stat5a(-/-)5b(-/-) embryos are severely anemic; erythroid progenitors are present in low numbers, show higher levels of apoptosis, and are less responsive to Epo. These findings are explained by a crucial role for Stat5 in EpoR's antiapoptotic signaling: it mediates the immediate-early induction of Bcl-X-L in erythroid cells through direct binding to the Bcl-X promoter.
引用
收藏
页码:181 / 191
页数:11
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