机构:[1]Department of Orthopaedics, Warren Alpert Medical School of Brown University/RIH, CORO West, Suite 402H, 1 Hoppin Street, Providence, RI 02903, USA.[2]Foot & Ankle Orthopaedic Surgery Center, Beijing Tongren Hospital, Capital Medical University, Beijing, China.首都医科大学附属北京同仁医院首都医科大学附属同仁医院[3]Department of Orthopaedics, the Second Hospital of Shanxi Medical University, Shanxi Key Lab of Bone and Soft Tissue Injury Repair, Taiyuan, China.
Background: The objective of this study was to evaluate the extent of stromal cell-derived factor-1's (SDF-1) involvement in the pathogenesis of idiopathic versus post-traumatic OA by comparing differences in synovial membrane morphology, SDF-1 synovial fluid (SF) concentrations, and matrix metalloproteinase-13 (MMP-13) SF concentrations. Methods: Thirty-six 3-month-old Hartley guinea pigs were obtained and divided into 6 groups. Upon sacrifice, India Ink staining was used to evaluate gross morphology, Safranin O/Fast green staining was used to assess cartilage damage, H/E staining was employed to visualize the synovium, and SF samples were obtained for biochemical analyses. Sandwich ELISA was used to quantify the SF concentrations of SDF-1 and MMP-13. Results: 12 month-old, idiopathic OA guinea pigs and 5.5 month-old ACLT animals had comparable cartilage damage when evaluated by the Modified Mankin Score. SDF-1 and MMP-13 concentrations were not statistically different between the two groups. The synovial membrane of the 5.5 month ACLT group had severe synovitis compared to the idiopathic OA group. Conclusion: In this study, it was found that synovial inflammation, independent of cartilage morphology, SDF-1 concentration, and MMP-13 concentration, was markedly different between idiopathic and post-traumatic OA. These results highlight the differing morphological and biochemical profiles of post-traumatic versus idiopathic osteoarthritis and calls for a more thorough examination of the sole of the synovial membrane in the pathogenesis of post-traumatic osteoarthritis.
基金:
Grant R01AR059142 from NIH/NIAMS and
P20GM104937 from NIH/NIGMS, NSFC 81071495, 81171676 and 31271033,
SXNSF 2011011042.
第一作者机构:[1]Department of Orthopaedics, Warren Alpert Medical School of Brown University/RIH, CORO West, Suite 402H, 1 Hoppin Street, Providence, RI 02903, USA.
共同第一作者:
通讯作者:
推荐引用方式(GB/T 7714):
Thomas Nathan P.,Wu Wesley J.,Fleming Braden C.,et al.Synovial inflammation plays a greater role in post-traumatic osteoarthritis compared to idiopathic osteoarthritis in the Hartley guinea pig knee[J].BMC MUSCULOSKELETAL DISORDERS.2017,18:doi:10.1186/s12891-017-1913-6.
APA:
Thomas, Nathan P.,Wu, Wesley J.,Fleming, Braden C.,Wei, Fangyuan,Chen, Qian&Wei, Lei.(2017).Synovial inflammation plays a greater role in post-traumatic osteoarthritis compared to idiopathic osteoarthritis in the Hartley guinea pig knee.BMC MUSCULOSKELETAL DISORDERS,18,
MLA:
Thomas, Nathan P.,et al."Synovial inflammation plays a greater role in post-traumatic osteoarthritis compared to idiopathic osteoarthritis in the Hartley guinea pig knee".BMC MUSCULOSKELETAL DISORDERS 18.(2017)