| Literature DB >> 28843170 |
Jie Sun1, Xuelei Wei2, Yandong Lu1, Meng Cui1, Fangguo Li1, Jie Lu1, Yunjiao Liu1, Xi Zhang1.
Abstract
GRX1 (glutaredoxin1), a sulfhydryl disulfide oxidoreductase, is involved in many cellular processes, including anti-oxidation, anti-apoptosis, and regulation of cell differentiation. However, the role of GRX1 in the oxidative stress and apoptosis of osteoarthritis chondrocytes remains unclear, prompting the current study. Protein and mRNA expressions were measured by Western blot and RT-qPCR. Oxidative stress was detected by the measurement of MDA and SOD contents. Cells apoptosis were detected by Annexin V-FITC/PI and caspase-3 activity assays. We found that the mRNA and protein expressions of GRX1 were significantly down-regulated in osteoarthritis tissues and cells. GRX1 overexpression increased the mRNA and protein expression of CREB and HO-1. Meanwhile, GRX1 overexpression inhibited oxidative stress and apoptosis in osteoarthritis chondrocytes. Furthermore, we found that GRX1 overexpression regulated HO-1 by increasing CREB, and that HO-1 regulated oxidative stress and apoptosis in osteoarthritis chondrocytes. Thus, GRX1 overexpression constrains oxidative stress and apoptosis in osteoarthritis chondrocytes by regulating CREB/HO-1, providing a novel insight into the molecular mechanism and potential treatment of osteoarthritis.Entities:
Keywords: Apoptosis; CREB; GRX1; HO-1; Osteoarthritis chondrocytes; Oxidative stress
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Year: 2017 PMID: 28843170 DOI: 10.1016/j.molimm.2017.08.006
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407