Timing of Intra-Articular Injection of Synovial Mesenchymal Stem Cells Affects Cartilage Restoration in a Partial Thickness Cartilage Defect Model in Rats

被引:18
作者
Enomoto, Takahiro [1 ]
Akagi, Ryuichiro [1 ]
Ogawa, Yuya [1 ,2 ]
Yamaguchi, Satoshi [3 ]
Hoshi, Hiroko [1 ]
Sasaki, Toshihide [1 ]
Sato, Yusuke [1 ]
Nakagawa, Ryosuke [1 ]
Kimura, Seiji [1 ,2 ]
Ohtori, Seiji [1 ]
Sasho, Takahisa [1 ,2 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Orthoped Surg, Chiba, Japan
[2] Chiba Univ, Ctr Prevent Med Sci, Musculoskeletal Dis, Chiba, Japan
[3] Chiba Univ, Coll Liberal Arts & Sci, Chiba, Japan
基金
日本学术振兴会;
关键词
partial thickness cartilage defects; mesenchymal stem cells; cartilage repair; synovium; ARTICULAR-CARTILAGE; OSTEOARTHRITIS; EPIDEMIOLOGY; INJURIES; BURDEN; REPAIR;
D O I
10.1177/1947603518786542
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
Objective We investigated the effect of administration of intra-articular mesenchymal stem cells (MSCs) on cartilage repair at different timings, and the distribution of MSCs in the knee. Design A partial thickness cartilage defect (PTCD) was created on the medial femoral condyle in 14-week-old Sprague-Dawley rats. Intra-articular injection of 1 x 10(6) MSCs was performed at 3 time points, namely at the time of surgery (0w group), at 1 week after surgery (1w group), and at 2 weeks after surgery (2w group). For the control, 50 mu L phosphate-buffered saline was injected at the time of surgery. The femoral condyles were collected at 6 weeks after creation of PTCD and assessed histologically. To investigate the distribution of MSCs, fluorescent-labeled MSCs were injected into the knee joint. Results In the control group, the cartilage lesion was distinguishable from surrounding cartilage. In the 0w group, hypocellularity and a slight decrease in safranin O stainability were observed around the injured area, but cartilage was restored to a nearly normal condition. In contrast, in the 1w and 2w groups, the cartilage surface was irregular and safranin O stainability in the injured and surrounding areas was poor. Histological score in the 0w group was significantly better than in the control, 1w, and 2w groups. At 1 day postinjection, fluorescent-labeled MSCs were mostly distributed in synovium. However, no migration into the PTCD was observed. Conclusions Early intra-articular injection of MSCs was effective in enhancing cartilage healing in a rat PTCD model. Injected MSCs were distributed in synovium, not in cartilage surrounding the PTCD.
引用
收藏
页码:122 / 129
页数:8
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