| Literature DB >> 17301822 |
E Dassé1, L Bridoux, T Baranek, E Lambert, S Salesse, M L Sowa, L Martiny, C Trentesaux, E Petitfrère.
Abstract
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 p38alpha 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/p38alpha pathway was activated downstream the caspase-3 in TIMP-1-induced hematopoietic differentiation.Entities:
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Year: 2007 PMID: 17301822 DOI: 10.1038/sj.leu.2404540
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528