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Modulation of matrix gelatinases and metalloproteinase-activating process in acute kidney rejection
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
Affiliation:Laboratory of Molecular Medicine, UQAM-Sainte-Justine Hospital, C.P. 8888, Succursale Centre-Ville Montreal, Quebec, H3C 3P8, Canada.
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.
Keywords:Kidney transplantation    Acute rejection    Extracellular matrix    MMP-2    TIMP-2    Urine
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