Activated macrophages down-regulate podocyte nephrin and podocin expression via stress-activated protein kinases

作者：Ikezumi Yohei^*; Suzuki Toshiaki; Karasaw Tamaki; Kawachi Hiroshi; Nikolic Paterson David J; Uchiyam Makoto

来源：Biochemical and Biophysical Research Communications, 2008, 376(4): 706-711.

DOI：10.1016/j.bbrc.2008.09.049

• TNF-alpha
• JNK
• p38 MAPK
• NF-kappa B
• IFN-gamma
• Cytoskeleton

The development of proteinuria and glomerulosclerosis in kidney disease is associated with podocyte damage, including down-regulation of nephrin and podocin. Macrophages are known to induce renal injury, but the mechanisms involved are not fully understood. This study examined macrophage-mediated podocyte damage. Conditioned media (CM) from activated macrophages caused a 50-60% reduction in nephrin and podocin nnRNA and protein expression in cultured mouse podocytes and rat glomeruli. This was abolished by a neutralizing anti-TNF alpha antibody. The addition of recombinant TNF alpha to podocytes OF glomeruli caused a comparable reduction in podocyte nephrin and podocin expression to that of macrophage CM. Inhibition of c-Jun amino terminal kinase (JNK) or p38 kinase abolished the TNF alpha-induced reduction in nephrin and podocin expression. This study demonstrates that activated macrophages can induce podocyte injury via a TNF alpha-JNK/p38-dependent mechanism. This may explain, in part, the protective effects of JNK and p38 blockade in experimental kidney disease.

• 出版日期2008-11-28