NDT Advance Access originally published online on July 31, 2007
Nephrology Dialysis Transplantation 2008 23(1):91-100; doi:10.1093/ndt/gfm509
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Blockage of JAK/STAT signalling attenuates renal ischaemia-reperfusion injury in rats
1Department of Nephrology and 2Department of Pediatrics, First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China
Correspondence to: Prof. Niansheng Yang, Department of Nephrology, First Affiliated Hospital, Sun Yat-Sen University, 58 Zhongshan Road II, Guangzhou 510080, P. R. China. Email: zsuyns{at}163.com or yangnsh{at}mail.sysu.edu.cn
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Abstract |
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Background. JAK/STAT signalling is one of the major pathways for cytokine signal transduction. However, the role of JAK/STAT in renal ischaemia/reperfusion (I/R) injury is not clear. The present study investigated the protection against renal I/R injury by in vivo inhibition of JAK2 activation.
Methods. Rats subjected to renal I/R were either treated with daily intraperitoneal injection of selective JAK2 inhibitor tyrphostin AG490 (10 mg/kg) or vehicle alone starting 4 h before, immediately after or until 3 h after I/R. Renal function, histology, infiltration of macrophages, apoptosis, expression of chemokines and adhesion molecules were assessed.
Results. AG490 treatment significantly inhibited the phosphorylation of JAK2 and its downstream molecule STAT1 and STAT3. Rats pretreated with AG490 exhibited improved renal function, attenuated histological lesions and reduced apoptosis of tubular epithelial cells. AG490 significantly inhibited renal expression of MCP-1 and ICAM-1 mRNA, as well as the expression of ICAM-1 protein, accompanied by decreased macrophage accumulation in the kidney. Immediate post-ischaemic treatment of AG490 also significantly ameliorated renal injury. However, delayed post-ischaemic treatment until 3 h after I/R failed to attenuate renal damage.
Conclusions. This study demonstrated the involvement of JAK/STAT signalling in the pathogenesis of renal I/R injury, suggesting that JAK/STAT pathway may serve as a potential target for early intervention in ischaemic acute renal failure.
Keywords: inflammation; ischaemia-reperfusion; kidney; macrophage
Received for publication: 8.10.06
Accepted in revised form: 3. 7.07
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