کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2107699 | 1083695 | 2010 | 13 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Matrix Metalloproteinase-9 Promotes Chronic Lymphocytic Leukemia B Cell Survival through Its Hemopexin Domain Matrix Metalloproteinase-9 Promotes Chronic Lymphocytic Leukemia B Cell Survival through Its Hemopexin Domain](/preview/png/2107699.png)
SummaryMatrix metalloproteinase-9 (MMP-9) is the major MMP produced by B-CLL cells and contributes to their tissue infiltration by degrading extracellular and membrane-anchored substrates. Here we describe a different function for MMP-9 in B-CLL, which involves the hemopexin domain rather than its catalytic function. Binding of soluble or immobilized (pro)MMP-9, a catalytically inactive proMMP-9 mutant, or the MMP-9 hemopexin domain to its docking receptors α4β1 integrin and CD44v, induces an intracellular signaling pathway that prevents B-CLL apoptosis. This pathway is induced in all B-CLL cases, is active in B-CLL lymphoid tissues, and consists of Lyn activation, STAT3 phosphorylation, and Mcl-1 upregulation. Our results establish that MMP/receptor binding induces intracellular survival signals and highlight the role of (pro)MMP-9 in B-CLL pathogenesis.
► MMP-9/integrin binding induces cell survival signaling by a noncatalytic mechanism
► Lyn, STAT3, and Mcl-1 are key and specific components of the MMP-9 survival pathway
► B-CLL cells in niches have higher surface MMP-9 and viability compared to those in PB
► MMP-9 has an additional function contributing to B-CLL pathogenesis
Journal: - Volume 17, Issue 2, 17 February 2010, Pages 160–172