Modulation of matrix gelatinases and metalloproteinase-activating process in acute kidney rejection |
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Authors: | Alain?Laplante,Dingyi?Liu,Michel?Demeule,Borhane?Annabi,Gerard?F.?Murphy,Pierre?Daloze,Huifang?Chen,Richard?Béliveau mailto:oncomol@nobel.si.uqam.ca" title=" oncomol@nobel.si.uqam.ca" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author |
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Affiliation: | Laboratory of Molecular Medicine, UQAM-Sainte-Justine Hospital, C.P. 8888, Succursale Centre-Ville Montreal, Quebec, H3C 3P8, Canada. |
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Abstract: | Changes in matrix metalloproteinase (MMP) activities would contribute to the accumulation of extracellular matrix during acute kidney allograft rejection. MMP-2 and MMP-9 and other gelatinolytic activities were examined in the rejected graft and the urine of a rat model of acute kidney rejection (orthotopic allotransplantation from a Buffalo donor to a Wistar-Furth recipient) by either zymography or fluorescence assay. MMP-2, membrane type 1 (MT1)-MMP, and tissue inhibitor of metalloproteinase (TIMP)-2 were also examined by immunodetection. The proMMP-2 activity and protein level increased in the graft during rejection when compared with normal Buffalo kidney, whereas activated MMP-2 decreased. TIMP-2 protein levels were markedly decreased and MT1-MMP proteolytic fragments (44-40 kDa) were undetectable. This suggests an altered MT1-MMP-dependent processing of proMMP-2 into active MMP-2 due to a diminished TIMP-2 level in acute kidney rejection. In the urine the overall gelatinolytic activity decreased considerably, although activity associated with an as yet unidentified 78-kDa protein appeared 6 days after transplantation. |
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Keywords: | Kidney transplantation Acute rejection Extracellular matrix MMP-2 TIMP-2 Urine |
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