Chawla Kanika, Klein Travis J, Schumacher Barbara L, Jadin Kyle D, Shah Bansari H, Nakagawa Koichi, Wong Van W, Chen Albert C, Masuda Koichi, Sah Robert L
Department of Bioengineering, University of California, San Diego, La Jolla, California 92093-0412, USA.
Tissue Eng. 2007 Jul;13(7):1525-37. doi: 10.1089/ten.2007.0044.
It is likely that effective application of cell-laden implants for cartilage defects depends on retention of implanted cells and interaction between implanted and host cells. The objectives of this study were to characterize stratified cartilaginous constructs seeded sequentially with superficial (S) and middle (M) chondrocyte subpopulations labeled with fluorescent cell tracking dye PKH26 () and determine the degree to which these stratified cartilaginous constructs maintain their architecture in vivo after implantation in mini-pigs for 1 week. Alginate-recovered cells were seeded sequentially to form stratified S/M (only S cells labeled) and S*/M* (both S and M cells labeled) constructs. Full-thickness defects (4 mm diameter) were created in the patellofemoral groove of adult Yucatan mini-pigs and filled with portions of constructs or left empty. Constructs were characterized biochemically, histologically, and biomechanically, and stratification visualized and quantified, before and after implant. After 1 week, animals were sacrificed and implants retrieved. After 1 week in vivo, glycosaminoglycan and collagen content of constructs remained similar to that at implant, whereas DNA content increased. Histological analyses revealed features of an early repair response, with defects filled with tissues containing little matrix and abundant cells. Some implanted (PKH26-labeled) cells persisted in the defects, although constructs did not maintain a stratified organization. Of the labeled cells, 126 +/- 38% and 32 +/- 8% in S*/M and S*/M* constructs, respectively, were recovered. Distribution of labeled cells indicated interactions between implanted and host cells. Longer-term in vivo studies will be useful in determining whether implanted cells are sufficient to have a positive effect in repair.
载细胞植入物在软骨缺损治疗中的有效应用可能取决于植入细胞的留存以及植入细胞与宿主细胞之间的相互作用。本研究的目的是对依次接种用荧光细胞追踪染料PKH26()标记的表层(S)和中层(M)软骨细胞亚群的分层软骨构建体进行表征,并确定这些分层软骨构建体在小型猪体内植入1周后其结构在体内的维持程度。将藻酸盐回收的细胞依次接种以形成分层的S/M(仅S细胞被标记)和S*/M*(S和M细胞均被标记)构建体。在成年尤卡坦小型猪的髌股沟中制造全层缺损(直径4毫米),并用构建体的部分填充或保持空的状态。在植入前后,对构建体进行生化、组织学和生物力学表征,并对分层进行可视化和定量分析。1周后,处死动物并取出植入物。在体内放置1周后,构建体的糖胺聚糖和胶原蛋白含量与植入时相似,而DNA含量增加。组织学分析揭示了早期修复反应的特征,缺损处充满了基质少而细胞丰富的组织。尽管构建体没有维持分层组织,但一些植入的(PKH26标记的)细胞在缺损处持续存在。在S*/M和S*/M*构建体中,分别回收了126±38%和32±8%的标记细胞。标记细胞的分布表明植入细胞与宿主细胞之间存在相互作用。长期的体内研究将有助于确定植入细胞是否足以对修复产生积极影响。