滑膜衬里巨噬细胞在实验性骨关节炎期间介导骨赘形成。
Synovial lining macrophages mediate osteophyte formation during experimental osteoarthritis.
作者信息
Blom Arjen B, van Lent Peter L E M, Holthuysen Astrid E M, van der Kraan Peter M, Roth Johannes, van Rooijen Nico, van den Berg Wim B
机构信息
Experimental Arthritis and Advanced Therapies, University Medical Center Nijmegen, The Netherlands.
出版信息
Osteoarthritis Cartilage. 2004 Aug;12(8):627-35. doi: 10.1016/j.joca.2004.03.003.
OBJECTIVE
In human osteoarthritis (OA), various forms of pathology are observed. Besides cartilage damage and fibrosis, neogenesis of bone, osteophyte formation, also occurs. Osteophytes are thought to limit joint movement and cause pain. The objective of this study was to investigate whether synovial macrophages are involved in osteophyte formation in experimental OA, and if they are, to study which mechanism may be involved.
DESIGN
Experimental OA was induced by two intra-articular injections of collagenase on alternate days into murine knee joints. The role of synovial lining macrophages in this model was studied by selective removal of these cells prior to OA induction using clodronate liposomes. After 1 and 2 weeks, knee joints were dissected and examined (immuno)histologically.
RESULTS
At days 7 and 14 after induction of OA, osteophyte formation and fibrosis were observed. Depletion of synovial macrophages resulted in spectacular reduction of osteophyte formation, 84% and 66%, respectively, at days 7 and 14. Fibrosis and synovial activation, measured by MRP8/14 expression, were also ameliorated (40-60%). In addition, production of growth factors (TGFbeta, BMP-2 and BMP-4) in the lining was largely prevented but production of these growth factors in deeper layers of the synovium and the periosteum did not differ from controls.
CONCLUSIONS
These results indicate the synovial macrophage to be a pivotal cell in the synovium mediating osteophyte formation and other OA-related pathology, like fibrosis, during experimental OA. Production of growth factors and induction of synovial activation by these cells may play a crucial role in this event.
目的
在人类骨关节炎(OA)中,可观察到多种病理形式。除了软骨损伤和纤维化外,还会出现骨新生和骨赘形成。骨赘被认为会限制关节活动并引起疼痛。本研究的目的是调查滑膜巨噬细胞是否参与实验性OA中的骨赘形成,如果参与,研究可能涉及哪种机制。
设计
通过每隔一天向小鼠膝关节内注射两次胶原酶来诱导实验性OA。在OA诱导前使用氯膦酸盐脂质体选择性去除这些细胞,研究滑膜衬里巨噬细胞在该模型中的作用。1周和2周后,解剖膝关节并进行(免疫)组织学检查。
结果
在OA诱导后的第7天和第14天,观察到骨赘形成和纤维化。滑膜巨噬细胞的耗竭导致骨赘形成显著减少,在第7天和第14天分别减少了84%和66%。通过MRP8/14表达测量的纤维化和滑膜活化也得到改善(40 - 60%)。此外,衬里中生长因子(TGFβ、BMP - 2和BMP - 4)的产生在很大程度上得到抑制,但滑膜深层和骨膜中这些生长因子的产生与对照组没有差异。
结论
这些结果表明滑膜巨噬细胞是滑膜中的关键细胞,在实验性OA期间介导骨赘形成和其他与OA相关的病理过程,如纤维化。这些细胞产生生长因子并诱导滑膜活化可能在这一过程中起关键作用。