Lam J, Lu S, Lee E J, Trachtenberg J E, Meretoja V V, Dahlin R L, van den Beucken J J J P, Tabata Y, Wong M E, Jansen J A, Mikos A G, Kasper F K
Department of Bioengineering, Rice University, P.O. Box 1892, MS-142, Houston, TX 77251-1892, USA.
Department of Biomaterials, Radboud umc, Nijmegen, The Netherlands.
Osteoarthritis Cartilage. 2014 Sep;22(9):1291-300. doi: 10.1016/j.joca.2014.06.035. Epub 2014 Jul 4.
To investigate the ability of cell-laden bilayered hydrogels encapsulating chondrogenically and osteogenically (OS) pre-differentiated mesenchymal stem cells (MSCs) to effect osteochondral defect repair in a rabbit model. By varying the period of chondrogenic pre-differentiation from 7 (CG7) to 14 days (CG14), the effect of chondrogenic differentiation stage on osteochondral tissue repair was also investigated.
Rabbit MSCs were subjected to either chondrogenic or osteogenic pre-differentiation, encapsulated within respective chondral/subchondral layers of a bilayered hydrogel construct, and then implanted into femoral condyle osteochondral defects. Rabbits were randomized into one of four groups (MSC/MSC, MSC/OS, CG7/OS, and CG14/OS; chondral/subchondral) and received two similar constructs bilaterally. Defects were evaluated after 12 weeks.
All groups exhibited similar overall neo-tissue filling. The delivery of OS cells when compared to undifferentiated MSCs in the subchondral construct layer resulted in improvements in neo-cartilage thickness and regularity. However, the addition of CG cells in the chondral layer, with OS cells in the subchondral layer, did not augment tissue repair as influenced by the latter when compared to the control. Instead, CG7/OS implants resulted in more irregular neo-tissue surfaces when compared to MSC/OS implants. Notably, the delivery of CG7 cells, when compared to CG14 cells, with OS cells stimulated morphologically superior cartilage repair. However, neither osteogenic nor chondrogenic pre-differentiation affected detectable changes in subchondral tissue repair.
Cartilage regeneration in osteochondral defects can be enhanced by MSCs that are chondrogenically and osteogenically pre-differentiated prior to implantation. Longer chondrogenic pre-differentiation periods, however, lead to diminished cartilage repair.
研究包裹软骨生成和成骨(OS)预分化间充质干细胞(MSC)的载细胞双层水凝胶修复兔模型骨软骨缺损的能力。通过将软骨生成预分化时间从7天(CG7)改变为14天(CG14),还研究了软骨生成分化阶段对骨软骨组织修复的影响。
将兔MSC进行软骨生成或成骨预分化,封装在双层水凝胶构建体的相应软骨层/软骨下骨层中,然后植入股骨髁骨软骨缺损处。将兔子随机分为四组之一(MSC/MSC、MSC/OS、CG7/OS和CG14/OS;软骨层/软骨下骨层),双侧接受两个相似的构建体。12周后评估缺损情况。
所有组的新生组织总体填充情况相似。与软骨下构建体层中未分化的MSC相比,OS细胞的递送使新生软骨厚度和规则性得到改善。然而,与对照组相比,在软骨层中添加CG细胞和在软骨下骨层中添加OS细胞并没有增强受后者影响的组织修复。相反,与MSC/OS植入物相比,CG7/OS植入物导致新生组织表面更不规则。值得注意的是,与CG14细胞相比,CG7细胞与OS细胞一起递送刺激了形态上更优的软骨修复。然而,成骨或软骨生成预分化均未影响软骨下组织修复的可检测变化。
植入前进行软骨生成和成骨预分化的MSC可增强骨软骨缺损中的软骨再生。然而,更长的软骨生成预分化时间会导致软骨修复减弱。