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1,25-Dihydroxyvitamin D Inhibits the Proliferation of Rat Mesangial Cells Induced by High Glucose Via DDIT4

Overview
Journal Oncotarget
Specialty Oncology
Date 2018 Feb 9
PMID 29416624
Citations 5
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Abstract

1,25-Dihydroxyvitamin D(1,25(OH) D) is a secosteroid with antiproliferative property. It also plays a pivotal renoprotective role in diabetic nephropathy. We investigated whether 1,25(OH)D could inhibit the proliferation of rat mesangial cells exposed to high glucose via the DNA-damage-inducible transcript 4/mammalian target of rapamycin(DDIT4/mTOR) pathway. The cell proliferation rate and cell cycle duration were measured using cell counting kit-8 assay and flow cytometry. Protein expression was assayed by Western blot. Glucose acted as a growth factor in rat mesangial cells, promoted cell proliferation. In parallel, the protein expression of DDIT4, TSC1/TSC2, and 4E-BP1 were decreased, and Rheb, mTOR, and p70S6K were increased. Acting via the DDIT4/mTOR signaling, 1,25(OH) D treatment reversed these pathological changes, upregulated DDIT4, TSC1/TSC2, and 4E-BP1, downregulated Rheb, mTOR, and p70S6K. The short-term overexpression of DDIT4 inhibited the proliferation of rat mesangial cells, similar to 1,25(OH) D treatment. siRNA knockdown of DDIT4 suppressed antiproliferative responses to 1,25(OH) D. These results suggest that 1,25(OH) D inhibits the proliferation of rat mesangial cells induced by high glucose via the DDIT4/mTOR signaling pathway.

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