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栀子苷通过体外抑制ERK信号通路对佐剂性关节炎大鼠成纤维样滑膜细胞的凋亡作用

Apoptotic Effect of Geniposide on Fibroblast-Like Synoviocytes in Rats with Adjuvant-Induced Arthritis via Inhibiting ERK Signal Pathway In Vitro.

作者信息

Li Rong, Cai Li, Tang Wen-Jian, Lei Chao, Hu Cheng-Mu, Yu Fang

机构信息

School of Pharmacy, Anhui Medical University, 81 Meishan Road, Hefei, China.

Department of Pathology, School of Basic Medicine, Anhui Medical University, 81 Meishan Road, Hefei, 230032, Anhui Province, China.

出版信息

Inflammation. 2016 Feb;39(1):30-38. doi: 10.1007/s10753-015-0219-9.

Abstract

Stimulating fibroblast-like synoviocyte (FLS) apoptosis in rheumatoid arthritis (RA) is a promising strategy for clinical treatment. Previous studies have confirmed that geniposide shows a certain anti-arthritic effect in vivo. However, whether geniposide can induce RA FLS apoptosis and the underlying mechanisms has not been elucidated. Herein, adjuvant-induced arthritis (AIA) in rat was induced and FLS was isolated from synovial tissues by tissue explant cultivation method. MTT assay, Hoechst staining, and flow cytometric apoptosis assay were applied to evaluate apoptotic effect of geniposide on AIA FLS. Bcl-2, Bax, and caspase 3 messenger RNA (mRNA) levels, and extracellular-signal-regulated kinases (ERKs) and phosphorylated ERK protein levels were examined by real-time PCR and western blot, respectively. We found that geniposide dose-dependently inhibited AIA FLS proliferation in vitro. AIA FLS treated with geniposide displayed typical apoptotic morphological characteristics including nuclear shrinkage and chromatin condensation. Flow cytometric apoptosis assay indicated that geniposide significantly increased the apoptosis rate of AIA FLS. Additionally, geniposide treatment on AIA FLS decreased Bcl-2 mRNA level and increased Bax and caspase 3 mRNA levels, accompanied by reduced protein levels of phosphorylated-ERK1/2, without affecting total ERK1/2. In conclusion, geniposide effectively induces AIA FLS apoptosis through regulating the apoptosis-related gene expressions and inhibiting ERK signal pathway.

摘要

刺激类风湿关节炎(RA)中滑膜成纤维样细胞(FLS)凋亡是一种很有前景的临床治疗策略。先前的研究已证实栀子苷在体内显示出一定的抗关节炎作用。然而,栀子苷是否能诱导RA-FLS凋亡及其潜在机制尚未阐明。在此,通过组织外植体培养法诱导大鼠佐剂性关节炎(AIA),并从滑膜组织中分离出FLS。采用MTT法、Hoechst染色和流式细胞术凋亡检测法评估栀子苷对AIA-FLS的凋亡作用。分别通过实时PCR和蛋白质印迹法检测Bcl-2、Bax和半胱天冬酶3信使核糖核酸(mRNA)水平,以及细胞外信号调节激酶(ERK)和磷酸化ERK蛋白水平。我们发现栀子苷在体外剂量依赖性地抑制AIA-FLS增殖。用栀子苷处理的AIA-FLS表现出典型的凋亡形态特征,包括核固缩和染色质凝聚。流式细胞术凋亡检测表明栀子苷显著提高了AIA-FLS的凋亡率。此外,对AIA-FLS进行栀子苷处理可降低Bcl-2 mRNA水平,提高Bax和半胱天冬酶3 mRNA水平,同时降低磷酸化ERK1/2的蛋白水平,而不影响总ERK1/2。总之,栀子苷通过调节凋亡相关基因表达和抑制ERK信号通路有效诱导AIA-FLS凋亡。

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