Abstract
OBJECTIVE: To further elucidate the mechanism of the anti-fibrogenic role of pigment epithelium-derived factor (PEDF) on diabetic nephropathy. METHODS: Human glomerular mesangial cells (HMCs) were treated with 30mmol/l D-glucose for different time intervals (6, 12, 24, and 48 hrs). To examine the beneficial effect of PEDF, we incubated the HMCs with high glucose (30mmol/L) in the presence of different concentrations of PEDF (10, 40, and 100nmol/l) for 24 hrs. The study took place in the Laboratory of Endocrinology, Renmin Hospital of Wuhan University, Wuhan, China between July 2012 and December 2012. Transforming growth factor-beta1 (TGF-beta1) and fibronectin (FN) mRNA was measured by reverse transcription-polymerase chain reaction (RT-PCR). The protein synthesis of TGF-beta1 and FN in the culture medium of HMC was detected by enzyme-linked immunosorbent assay. The phosphorylation levels of Janus kinase2 (JAK2) and signal transducers and activators of transcription1 (STAT1) were measured using western blotting. RESULTS: The exposure of HMCs to 30 mmol/L glucose caused the activation of JAK2 and STAT1. It upregulated TGF-beta1 expression and increased protein synthesis of FN. These high glucose-induced changes were suppressed by PEDF. CONCLUSION: The PEDF can decrease the expression of TGF-beta1 and FN, possibly by inhibiting the phosphorylation of JAK/STAT, which may offer a promising strategy in the treatment of diabetic nephropathy.
Article Type
Research Article
First Page
793
Last Page
800
Recommended Citation
Mao, Tuohua; Chen, Hongmin; Hong, Lian; and Li, Jing
(2013)
"Pigment epithelium-derived factor inhibits high glucose-induced JAK/STAT signalling pathway activation in human glomerular mesangial cells,"
Saudi Medical Journal: Vol. 34:
Iss.
8, Article 2.
DOI: https://doi.org/10.15537/1658-3175.5798