Department of Orthopedic Surgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
J Shoulder Elbow Surg. 2013 Aug;22(8):1037-45. doi: 10.1016/j.jse.2012.11.005. Epub 2012 Dec 14.
This study examined whether a mesenchymal stem cells (MSCs)-seeded 3-dimensional construct into a tendon defect would promote cellular differentiation and matrix healing.
Bone marrow was harvested from the iliac crests of 2 male New Zealand White rabbits. The MSCs were cultured, and an open-cell polylactic acid (OPLA) scaffold was encapsulated with these cells. The injury model was a 5-mm × 5-mm-sized full-thickness window defect in the central part of each rotator cuff tendon. The defects on the right side were grafted with the autologous MSCs-seeded OPLA scaffold implant and a biodegradable suture. The same procedure was done on the left side, except a cell-free OPLA scaffold was used. Three rabbits were used as controls, without treatment of the tendon defect. Samples were harvested at 2, 4, and 6 weeks for analysis, which included evaluation of gross morphology, fluorescent analysis, histologic assessment, and immunohistochemistry studies.
The expression of immunohistochemical stainings for collagen I was higher in the scaffold with MSCs than in the scaffold without MSCs. The expression of collagen II, however, was not different between the scaffolds with and without MSCs.
Even though this is a short-term study, we demonstrated that many MSCs in the scaffold survived after implantation in an acute rabbit rotator cuff defect. Furthermore, the generation of type I collagen increased more in the scaffold with MSCs than it did in the scaffold without MSCs. MSCs are thought to promote tendon healing by producing type I collagen when they are applied at the tendon defect.
本研究旨在探讨骨髓间充质干细胞(MSCs)接种于 3D 构建物中是否能促进细胞分化和基质愈合。
从 2 只雄性新西兰白兔的髂嵴采集骨髓。培养 MSCs 并将其包裹在开孔聚乳酸(OPLA)支架中。损伤模型为每个肩袖肌腱中心部分的 5mm×5mm 全层窗口缺损。右侧缺损用自体 MSCs 接种的 OPLA 支架移植物和可生物降解缝线进行移植。左侧采用相同的方法,但使用无细胞的 OPLA 支架。3 只兔子作为对照,不治疗肌腱缺损。分别在 2、4 和 6 周时采集样本进行分析,包括大体形态评估、荧光分析、组织学评估和免疫组织化学研究。
MSCs 接种支架的Ⅰ型胶原免疫组织化学染色表达高于无 MSCs 接种支架。然而,支架有无 MSCs 对Ⅱ型胶原的表达无影响。
尽管这是一项短期研究,但我们已经证明,在急性兔肩袖缺损中,支架内有许多 MSCs 存活下来。此外,在有 MSCs 接种的支架中,Ⅰ型胶原的生成量多于无 MSCs 接种的支架。MSCs 被认为可以通过在肌腱缺损处产生Ⅰ型胶原来促进肌腱愈合。