Tissue inhibitor of metalloproteinase-1 promotes hematopoietic differentiation via caspase-3 upstream the MEKK1/MEK6/p38α pathway

被引:29
|
作者
Dasse, E.
Bridoux, L.
Baranek, T.
Lambert, E.
Salesse, S.
Sowa, M. L.
Martiny, L.
Trentesaux, C.
Petitfrere, E.
机构
[1] UFR Sci Exactes & Nat, Biochim Lab, CNRS 6198, IFR Biomol 53, F-51687 Reims, France
[2] UFR Pharm, EA, IPCM 3796, Reims, France
[3] UFR Sci, EA 3796, Biol Cellulaire & Mol Lab, Reims, France
[4] UFR Pharm, JE 2428, IFR Biomol 53, Reims, France
关键词
TIMP-1; hematopoietic differentiation; caspase-3; MEKK1; MEK6; p38; alpha;
D O I
10.1038/sj.leu.2404540
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Besides its matrix metalloproteinases inhibitory activity, TIMP-1 exhibits other biological activities such as cell survival and proliferation. The intracellular signalling pathway elicited by TIMP-1 begins to be elucidated. We have shown previously that the caspase-3 and the p38a MAP kinase were activated during TIMP-1-induced UT-7 cells erythroid differentiation. In this study, we demonstrated that TIMP-1 differentiating effect can be extended to the IL-3-dependent myeloid murine 32D cell line and human erythroid progenitors derived from cord blood CD34(+) cells. By performing small interfering RNA transfection and using chemical inhibitors, we evidenced that caspase-3 was involved in TIMP-1 differentiating effect. We then identified the MEKK1 kinase as a caspase-3 substrate and demonstrated that the MEKK1/MEK6/p38 alpha pathway was activated downstream the caspase-3 in TIMP-1-induced hematopoietic differentiation.
引用
收藏
页码:595 / 603
页数:9
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