Dramatic early event in chronic allograft nephropathy: increased but not decreased expression of MMP-9 gene
- Equal contributors
1 Department of Nephrology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, 510630, People’s Republic of China
2 Department of Nephrology, Wenzhou Medical College, Wenzhou, 325035, People’s Republic of China
3 Department of Cardiovascular Medicine, The Third Affiliated Hospital of Southern Medical University, Guangzhou, 510515, People’s Republic of China
Diagnostic Pathology 2013, 8:13 doi:10.1186/1746-1596-8-13Published: 28 January 2013
The infiltration of mononuclear cells and replication and migration of smooth muscle cells (SMCs) from media into the intima in the vascular wall are the cardinal pathological changes in the early stage of chronic allograft nephropathy (CAN). But the mechanism is unclear. Therefore we investigated the role of matrix metalloproteinase 9 (MMP-9) and its interaction with TGF-beta1, tubulointerstitial mononuclear cells infiltration and migration of SMCs in the early stage of CAN.
Kidneys of Fisher (F334) rats were orthotopically transplanted into bilaterally nephrectomized Lewis (LEW) recipients. To suppress an initial episode of acute rejection, rats were briefly treated with cyclosporine A (1.5 mg/kg/day) for the first 10 days. Animals were harvested at 12 weeks after transplantation for histological, immunohistochemistry and molecular biological analysis.
The expression of MMP-9 was up-regulated in interstitium and vascular wall in the early stage of CAN, where there were interstitial mononuclear cells infiltration and SMCs migration and proliferation. Moreover the expression of MMP-9 were positively correlated with the degree of interstitial mononuclear cells infiltration, the quantity of SMCs in arteriolar wall, and also the increased TFG-beta1 expression in the tubulointerstitium and arteriolar wall.
MMP-9 may play an important role in the mechanism of pathological changes during the earlier period of CAN.
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