Efficient inhibition of fibroblast proliferation and collagen expression by ERK2 siRNAs

被引:31
|
作者
Li, Fengfeng [1 ]
Fan, Cunyi [1 ]
Cheng, Tao [1 ]
Jiang, Chaoyin [1 ]
Zeng, Bingfang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Affiliated Peoples Hosp 6, Dept Orthopaed, Sch Med, Shanghai 200233, Peoples R China
关键词
Joint adhesion; Fibroblast; Small interfering RNA; ERK2; TGF-beta; 1; FGF-2; ACTIVATED PROTEIN-KINASE; RNA INTERFERENCE; LENTIVIRAL VECTORS; TRANSGENES; ROLES; SMAD3; MODEL; ACID;
D O I
10.1016/j.bbrc.2009.02.165
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transforming growth factor-beta 1 and fibroblast growth factor-2 play very important roles in fibroblast proliferation and collagen expression. These processes lead to the formation of joint adhesions through the SMAD and MAPK pathways, in which ERK2 is Supposed to be crucial. Based on these assumptions, lentivirus (LV)-mediated small interfering RNAs (siRNAs) targeting ERK2 were used to suppress the proliferation and collagen expression of rat joint adhesion tissue fibroblasts (RJATFs). Among four siRNAs examined, siRNA1 caused an 84% reduction in ERK2 expression (p < 0.01) and was selected as the most efficient siRNA for use in this study. In Subsequent experiments, significant downregulation of types I and III collagen were observed by quantitative RT-PCR and Western blot analyses. MTT assays and flow cytometry revealed marked inhibition of RJATF proliferation, but no apoptosis. in conclusion, LV-mediated ERK2 siRNAs may represent novel therapies or drug targets for preventing joint adhesion formation. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:259 / 263
页数:5
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