Synovial fluid recruits human mesenchymal progenitors from subchondral spongious bone marrow

被引:52
作者
Endres, Michaela
Neumann, Katja
Haeupl, Thomas
Erggelet, Christoph
Ringe, Jochen
Sittinger, Michael
Kaps, Christian
机构
[1] TransTissue Technol GmbH, D-10117 Berlin, Germany
[2] Univ Med Berlin, Dept Rheumatol, Tissue Engn Lab, Charite, D-10117 Berlin, Germany
[3] Univ Freiburg, Dept Orthopaed Surg & Traumatol, Freiburg, Germany
[4] Univ Med Berlin, Charite, Tissue Engn Lab, D-10117 Berlin, Germany
[5] Univ Med Berlin, Charite, Dept Rheumatol & Clin Immunol, Berlin Brandenburg Ctr Regenerat Therapies, D-10117 Berlin, Germany
关键词
cell recruitment; microfracture; synovial fluid; osteoarthritis; chemotaxis;
D O I
10.1002/jor.20394
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
摘要
Microfracture is a frequently used reparative technique that induces a healing response in articular cartilage defects. Penetration of the subchondral bone leads to blood clot formation, allows multipotent mesenchymal cells to access the defect and, subsequently, leads to cartilaginous repair tissue. The aim of our study was to analyze the chemotactic recruitment of human subchondral spongious bone marrow-derived cells by synovial fluid (SF) from normal donors (ND), patients with osteoarthritis (OA) and rheumatoid arthritis (RA). Subchondral spongious bone marrow-derived mesenchymal progenitors were isolated from bone cylinders after high tibial osteotomy and analyzed for the presence of stem cell-related cell surface antigens by flowcytometry. Recruitment of subchondral progenitors by normal SF and SF from donors with degenerated joint diseases was documented by using a modified Boyden chamber chemotaxis assay. The chemotaxis assay demonstrated that synovial fluid has the potential to recruit mesenchymal progenitors in vitro. SF from normal donors and patients with OA showed no difference in the potential to stimulate cell migration. SF obtained from RA donors showed significantly reduced cell recruitment compared to SF derived from OA patients (p = 0.0054) and normal donors (p < 0.0001). The chemotactic activity of SF obtained from normal donors and from patients with degenerative joint diseases suggests that SF may be actively involved in the migration of progenitors in cartilage defects after microfracture. (c) 2007 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.
引用
收藏
页码:1299 / 1307
页数:9
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