Role of TRB3 in the inhibitory effect of fenofibrate against high glucose-induced proliferation of glomerular mesangial cells.
- Author:
Qingqing SONG
1
;
Jia SUN
;
Jiao WANG
;
Rui YANG
;
Rongping CHEN
;
Zhen ZHANG
;
Haizhao LUO
;
Dehong CAI
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Cell Cycle Checkpoints; Cell Proliferation; drug effects; Cells, Cultured; Fenofibrate; pharmacology; Glucose; adverse effects; metabolism; Mesangial Cells; cytology; drug effects; Phosphorylation; Protein-Serine-Threonine Kinases; antagonists & inhibitors; metabolism; Proto-Oncogene Proteins c-akt; metabolism; Rats; Signal Transduction
- From: Journal of Southern Medical University 2013;33(3):391-396
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the role of TRB3 in the inhibitory effect of fenofibrate against the proliferation of glomerular mesangial cell induced by high glucose.
METHODSRat glomerular mesangial cells (MCs) were cultured in the presence of 5.5 mmol/L glucose (normal control), 25 mmol/L glucose (high glucose group), or high glucose along with 10, 50, or 100 µmol/L fenofibrate. Cell counting kit-8 (CCK-8) assay was used to evaluate cell proliferation, and Hoechst 33258 staining was employed to determine chromatin distribution in the MCs. Flow cytometry was performed to analyze the cell cycle changes in different groups. The expressions of TRB3 and P-AKT in different groups were detected using immunocytochemistry and Western blotting.
RESULTSHigh glucose induced obvious proliferation of the MCs (P<0.001), which was significantly inhibited by fenofibrate in a concentration-dependent manner (P<0.001). The MCs exposed to fenofibrate presented with typical apoptotic morphologies and cell cycle arrest at G1/S phase. Low levels of TRB3 expression was detected in the normal control and high glucose groups, whereas in the 3 fenofibrate groups, TRB3 expression increased and P-AKT expression decreased as fenofibrate concentration increased.
CONCLUSIONFenofibrate can promote TRB3 expression in rat MCs. TRB3 causes cell cycle arrest at G1/S phase by inhibiting AKT phosphorylation to result in suppressed proliferation of the MCs.