The influence of connective tissue growth factor on rabbit ligament injury repair. Issue 7 (July 2017)

• Record Type: Journal Article
• Authors: Sun, X.; Liu, W.; Cheng, G.; Qu, X.; Bi, H.; Cao, Z.; Yu, Q.
• Is Part Of: Bone & joint research. Volume 6:Issue 7(2017)
• Page Start: 399
• Page End: 404
• Publication Date: 2017-07
• Subjects: Anterior cruciate ligament -- Connective tissue growth factor -- TGF-β1; Musculoskeletal system -- Periodicals; 573.705
• DOI: 10.1302/2046-3758.67.BJR.2016-0255.R1
• Languages: English
• ISSNs: 2046-3758

Abstract

Abstract : Objectives: The injured anterior cruciate ligament (ACL) is thought to exhibit an impaired healing response, and attempts at surgical repair have not been successful. Connective tissue growth factor (CTGF) is reported to be associated with wound healing, probably through transforming growth factor beta 1 (TGF-β1). Methods: A rabbit ACL injury model was used to study the effect of CTGF on ligament recovery. Quantitative real-time PCR (qRT-PCR) was performed for detection of changes in RNA levels of TGF-β1, type 1 collagen (COL1), type 2 collagen (COL2), SRY-related high mobility group-box gene9 (SOX9), tissue inhibitor of metalloproteinase-1 (TIMP-1) and matrix metallopeptidase 13 (MMP-13). Expression of related proteins was detected by Western blotting. Results: The current study showed that CTGF could promote the recovery of an injured anterior cruciate ligament. It can upregulate mRNA and expression of TGF-β1, COL1, COL2, SOX9, and tissue inhibitor of TIMP-1, and downregulate mRNA and expression of MMP-13, suggesting that the curative effect of CTGF on injured rabbit ligaments is through regulation of these cellular factors. Conclusions: This finding revealed the healing role of CTGF in injured tissues and provides new possibilities of treating injured tissues and wound healing by using CTGF. Cite this article: X. Sun, W. Liu, G. Cheng, X. Qu, H. Bi, Z. Cao, Q. Yu. The influence of connective tissue growth factor on rabbit ligament injury repair. Bone Joint Res 2017;6:399–404. DOI: 10.1302/2046-3758.67.BJR.2016-0255.R1.