Efficient inhibition of fibroblast proliferation and collagen expression by ERK2 siRNAs
- 1. Department of Orthopaedics, The Sixth Affiliated People's Hospital, Shanghai Jiaotong University School of Medicine, 600 Yishan Road, Shanghai 200233 (China)
Description
Transforming growth factor-β1 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.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.bbrc.2009.02.165Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2009.02.165;
- PII
- S0006-291X(09)00427-6;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 382
- Journal Issue
- 2
- Journal Page Range
- p. 259-263
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45020493
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ANIMAL TISSUES; APOPTOSIS; COLLAGEN; DRUGS; FIBROBLASTS; GROWTH FACTORS; INHIBITION; POLYMERASE CHAIN REACTION; RATS; RNA; THERAPY
- Descriptors DEC
- ANIMAL CELLS; ANIMALS; BODY; CONNECTIVE TISSUE CELLS; GENE AMPLIFICATION; MAMMALS; MEDICINE; MITOGENS; NUCLEIC ACIDS; ORGANIC COMPOUNDS; PROTEINS; RODENTS; SCLEROPROTEINS; SOMATIC CELLS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.