Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2051500 | FEBS Letters | 2007 | 6 Pages |
Abstract
Expression of nephrin, a crucial component of the glomerular slit diaphragm, is downregulated in patients with proteinuric glomerular diseases. Using conditionally immortalized reporter podocytes, we found that bystander macrophages as well as macrophage-derived cytokines IL-1β and TNF-α markedly suppressed activity of the nephrin gene promoter in podocytes. The cytokine-initiated repression was reversible, observed on both basal and inducible expression, independent of Wilms’ tumor suppressor WT1, and caused in part via activation of the phosphatidylinositol-3-kinase/Akt pathway. These results indicated a novel mechanism by which activated macrophages participate in the induction of proteinuria in glomerular diseases.
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Authors
Yosuke Takano, Kozue Yamauchi, Kunihiro Hayakawa, Nobuhiko Hiramatsu, Ayumi Kasai, Maro Okamura, Makiko Yokouchi, Akihiro Shitamura, Jian Yao, Masanori Kitamura,