Lithium induces c-Ret expression in mouse inner medullary collecting duct cells
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- 作者：Nobuhiko Kojima ; Hiroshi Saito ; Masaki Nishikawa ; Shunsuke Yuri ; Oak Don Jo ; Phuong-Chi Pham ; Naomi Yanagawa ; Norimoto Yanagawa
- 关键词：mIMCD-3 cells ; c-Ret ; Lithium ; GSK-3β ; mTOR ; Rapamycin
- 刊名：Cellular Signalling
- 出版年：2011
- 出版时间：February 2011
- 年：2011
- 卷：23
- 期：2
- 页码：371-379
- 全文大小：864 K
文摘
We found in our present study that lithium (Li+) induced the expression of endogenous c-Ret, a tyrosine kinase receptor, in murine inner medullary collecting duct (mIMCD-3) cells. Delineation of the promoter region required for the effect of Li+ identified a positive regulatory element within 180 bp upstream of the transcription initiation site. This region contained three putative GC-rich Sp1 binding sites found to be essential for c-Ret induction by Li+. The effect of Li+ was mediated through glycogen synthase kinase 3β (GSK-3β) inhibition, although there was no biding site for T cell factor/lymphoid enhancer factor (TCF/LEF) in the 180 bp. We found that Li+ activated the mammalian target of rapamycin (mTOR) pathway via GSK-3β in these cells, and the effect of Li+ to induce c-Ret was amenable to the inhibitory effect of the mTOR inhibitor, rapamycin. We also found that alterations in both cellular β-catenin levels and mTOR activities affected the effect of Li+ on c-Ret transcription in a cooperative manner. In summary, our results show that Li+ can induce c-Ret expression in mIMCD-3 cells through both β-catenin- and mTOR-dependent pathways downstream of GSK-3β inhibition, which act synergistically on the GC-rich Sp1 binding elements in the promoter region.