Lithium induces c-Ret expression in mouse inner medullary collecting duct cells

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 3 beta (GSK-3 beta) 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-3 beta 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 beta-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 beta-catenin- and mTOR-dependent pathways downstream of GSK-3 beta, inhibition, which act synergistically on the GC-rich Sp1 binding elements in the promoter region. (C) 2010 Elsevier Inc. All rights reserved.