Integrin α1β1 protects against signs of post-traumatic osteoarthritis in the female murine knee partially via regulation of epidermal growth factor receptor signalling

被引:29
作者
Shin, S. Y. [1 ]
Pozzi, A. [2 ,3 ]
Boyd, S. K. [4 ,5 ]
Clark, A. L. [1 ,5 ,6 ]
机构
[1] Univ Calgary, Fac Kinesiol, Calgary, AB, Canada
[2] Vanderbilt Univ, Dept Med, Nashville, TN USA
[3] Vet Affairs Hosp, Dept Med, Nashville, TN USA
[4] Univ Calgary, Dept Radiol, Fac Med, Calgary, AB, Canada
[5] Univ Calgary, McCaig Inst Bone & Joint Hlth, Calgary, AB, Canada
[6] Univ Calgary, Dept Surg, Fac Med, Calgary, AB, Canada
基金
加拿大健康研究院; 美国国家卫生研究院; 加拿大自然科学与工程研究理事会;
关键词
Osteoarthritis; Experimental arthritis; Animal model; Cartilage degradation; Computed tomography; FACTOR-BETA; EXPRESSION; MODEL; JOINT; ACTIVATION; CARTILAGE; ERLOTINIB; ESTROGEN; CHONDROCYTES; PROGRESSION;
D O I
10.1016/j.joca.2016.05.013
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Objective: To investigate the role of integrin alpha 1 beta 1 in the progression of post-traumatic osteoarthritis (PTOA), and elucidate the contribution of epidermal growth factor receptor (EGFR) signalling to the mechanism by which integrin alpha 1 beta 1 might control PTOA. We hypothesised that integrin alpha 1 beta 1 plays a protective role in the course of PTOA and that the effect of PTOA (e.g., synovitis, loss of cartilage and growth of osteophytes) would be exacerbated in mice lacking integrin alpha 1 beta 1 at every time point post destabilisation of medial meniscus (DMM). Methods: DMM or sham surgery was performed on integrin alpha 1-null and wild type (WT) mice and the progression of PTOA analysed at 2, 4, 8 and 12 weeks post-surgery (PS) using micro-computed tomography (microCT), histology, and immunohistochemistry. In addition, the effects of EGFR blockade were examined by treating the mice with the EGFR inhibitor erlotinib. Results: Integrin alpha 1-null female, but not male, mice showed earlier cartilage degradation post DMM surgery compared to WT controls. Furthermore, erlotinib treatment resulted in significantly less cartilage damage in integrin alpha 1-null but not WT mice. Independent of genotype, erlotinib treatment significantly mitigated the effects of PTOA on many tissues of female mice including meniscal and fabella bone volume, subchondral bone thickness and density and cartilage degradation. In contrast, reduced EGFR signalling had little effect on signs of PTOA in male mice. Conclusion: Integrin alpha 1 beta 1 protects against PTOA-induced cartilage degradation in female mice partially via the reduction of EGFR signalling. Furthermore, reduction of EGFR signalling protects against the development of PTOA in female, but not male mice. (C) 2016 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1795 / 1806
页数:12
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