Signal transducer and activator of transcription 5a (STAT5a) is required for eosinophil differentiation of human cord blood-derived CD34+ cells

被引:48
作者
Buitenhuis, M [1 ]
Baltus, B [1 ]
Lammers, JWJ [1 ]
Coffer, PJ [1 ]
Koenderman, L [1 ]
机构
[1] Univ Utrecht, Med Ctr, Dept Pulm Dis, NL-3584 CX Utrecht, Netherlands
关键词
D O I
10.1182/blood-2002-03-0740
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Signal transducers and activators of transcription (STATs) have been reported to play a critical role in the differentiation of several myelold cell lines, although the importance of STATS In the differentiation of primary human hematopoietic cells remains to be established. Terminal eosinophil differentiation is induced by interleukin-5 (IL-5), which has also been demonstrated to activate STAT5. We have investigated whether STAT5 plays a critical role during eosinophil differentiation using umbilical cord blood-derived CD34(+) cells. In this ex vivo system, STAT5 expression and activation are high early during differentiation, and STAT5 protein expression is down-regulated during the final stages of eosinophil differentiation. Retroviral transductions were performed to ectopically express wild-type and dominant-negative STAT5a (STAT5aDelta750) in CD34(+) cells. Transduction of cells with STAT5a resulted in enhanced proliferation compared with cells transduced with empty vector alone. Interestingly, ectopic expression of STAT5a also resulted in accelerated differentiation. In contrast, ectopic expression of STAT5aDelta750 re-suited in a block in differentiation, whereas proliferation was also severely inhibited. Similar results were obtained with dominant-negative STAT5b. Forced expression of STAT5a enhanced expression of the STATS target genes Bcl-2 and p21(WAF/ClP1), suggesting they may be important in STMa-mediated eosinophil differentiation. These results demonstrate that STAT5 plays a critical role in eosinophil differentiation of primary human hematopoietic cells. (C) 2003 by The American Society of Hematology.
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页码:134 / 142
页数:9
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