Bushen-Qiangdu-Zhilv decoction inhibits osteogenic differentiation of rat fibroblasts by regulating connexin 43
Autor: | Run‑Yue Huang, Xiao‑Hong He, Ying‑Yan Zhou, Jie‑Hua Lin, Yong‑Yue Xu, Yi‑Ting He |
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Rok vydání: | 2016 |
Předmět: |
030203 arthritis & rheumatology
0301 basic medicine Cancer Research medicine.medical_specialty Oncogene medicine.diagnostic_test Cell Connexin Osteoblast Articles General Medicine Cell cycle Biology Molecular medicine Cell biology 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Endocrinology medicine.anatomical_structure Immunology and Microbiology (miscellaneous) Western blot Internal medicine medicine Fibroblast |
Zdroj: | Experimental and Therapeutic Medicine. 12:347-353 |
ISSN: | 1792-1015 1792-0981 |
DOI: | 10.3892/etm.2016.3292 |
Popis: | Bushen-Qiangdu-Zhilv (BQZ) decoction is a traditional Chinese medicinal compound widely used for treating ankylosing spondylitis (AS). However, the mechanisms underlying effects of BQZ remain largely unknown. Osteoblast differentiation of fibroblasts plays an important role in heterotopic ossification (HO) of AS, and connexin 43 (Cx43) is crucially involved in the osteoblast differentiation of fibroblasts. The aim of the present study was to evaluate the effects of BQZ on the osteogenic differentiation of fibroblasts by regulating Cx43. Rat fibroblasts were treated with freeze-dried powder of BQZ, in the presence or absence of recombinant human bone morphogenetic protein-2 (rhBMP-2). MTS assays were performed to examine the inhibitory effects of BQZ on fibroblast proliferation. Western blot assays were conducted to detect the protein expression of core-binding factor alpha 1 (Cbfα1), Cx43 and phosphorylated Cx43 (pCx43). BQZ appeared to inhibit fibroblast proliferation in a dose-dependent manner. Furthermore, the expression of Cbfα1 and Cx43/pCx43 was significantly suppressed by BQZ, with or without rhBMP-2 stimulation. Therefore, the present results indicate that BQZ may exert an anti-AS effect by suppressing the osteogenic differentiation of fibroblasts via Cx43 regulation. |
Databáze: | OpenAIRE |
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