𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Autologous synovial fluid enhances migration of mesenchymal stem cells from synovium of osteoarthritis patients in tissue culture system

✍ Scribed by Sheng Zhang; Takeshi Muneta; Toshiyuki Morito; Tomoyuki Mochizuki; Ichiro Sekiya


Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
330 KB
Volume
26
Category
Article
ISSN
0736-0266

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Synovial fluid from osteoarthritic knee contains mesenchymal stem cells (MSCs). One of the possible reservoirs of MSCs in synovial fluid is synovial tissue, and synovial fluid may induce mobilization of MSCs into synovial fluid in osteoarthritis patients. Here, we investigated whether synovial fluid expanded synovial MSCs in a tissue culture system. Human synovium and synovial fluid were obtained from osteoarthritis patients during total knee arthroplasties. In the tissue culture system, autologous synovial fluid expanded synovial cells statistically higher than αMEM + FBS, and the addition of TGFβ3 to αMEM + FBS increased expansion to a similar level in all 11 donors. The addition of decorin or anti‐TGFβ neutralizing antibody to synovial fluid partially inhibited synovial cell expansion. In cell culture assay, synovial fluid proliferated synovial cells fewer than αMEM + FBS. The expanded synovial cells in synovial fluid retained multipotentiality and showed surface markers similar to those of MSCs. We demonstrated that autologous synovial fluid enhanced expansion of MSCs in tissue culture of synovium from osteoarthritis patients by promoting cell migration. This effect was partially affected by TGFβ. © 2008 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 26:1413–1418, 2008


📜 SIMILAR VOLUMES


Novel insights into the mechanism of dec
✍ Alain Petit; Hong Tian Wang; Pierre-Luc Girard-Lauriault; Michael R. Wertheimer; 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 413 KB 👁 1 views

## Abstract Recent evidence indicates that a major drawback of current cartilage‐ and intervertebral disc (IVD) tissue engineering is that human mesenchymal stem cells (MSCs) from patients with osteoarthritis rapidly express type X collagen (COL10A1), a marker of late stage chondrocyte hypertrophy