Li Lei, Newton Phillip T, Bouderlique Thibault, Sejnohova Marie, Zikmund Tomas, Kozhemyakina Elena, Xie Meng, Krivanek Jan, Kaiser Jozef, Qian Hong, Dyachuk Vyacheslav, Lassar Andrew B, Warman Matthew L, Barenius Björn, Adameyko Igor, Chagin Andrei S
Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Central European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
FASEB J. 2017 Mar;31(3):1067-1084. doi: 10.1096/fj.201600918R. Epub 2016 Dec 13.
Articular cartilage has little regenerative capacity. Recently, genetic lineage tracing experiments have revealed chondrocyte progenitors at the articular surface. We further characterized these progenitors by using genetic approaches. Histone H2B-green fluorescent protein retention revealed that superficial cells divide more slowly than underlying articular chondrocytes. Clonal genetic tracing combined with immunohistochemistry revealed that superficial cells renew their number by symmetric division, express mesenchymal stem cell markers, and generate chondrocytes both asymmetric and symmetric differentiation. Quantitative analysis of cellular kinetics, in combination with phosphotungstic acid-enhanced micro-computed tomography, showed that superficial cells generate chondrocytes and contribute to the growth and reshaping of articular cartilage. Furthermore, we found that cartilage renewal occurs as the progeny of superficial cells fully replace fetal chondrocytes during early postnatal life. Thus, superficial cells are self-renewing progenitors that are capable of maintaining their own population and fulfilling criteria of unipotent adult stem cells. Furthermore, the progeny of these cells reconstitute adult articular cartilage entirely substituting fetal chondrocytes.-Li, L., Newton, P. T., Bouderlique, T., Sejnohova, M., Zikmund, T., Kozhemyakina, E., Xie, M., Krivanek, J., Kaiser, J., Qian, H., Dyachuk, V., Lassar, A. B., Warman, M. L., Barenius, B., Adameyko, I., Chagin, A. S. Superficial cells are self-renewing chondrocyte progenitors, which form the articular cartilage in juvenile mice.
关节软骨的再生能力较弱。最近,遗传谱系追踪实验揭示了关节表面存在软骨细胞祖细胞。我们通过遗传学方法进一步对这些祖细胞进行了表征。组蛋白H2B-绿色荧光蛋白保留实验表明,表层细胞的分裂速度比其下方的关节软骨细胞慢。克隆遗传追踪结合免疫组织化学表明,表层细胞通过对称分裂更新其数量,表达间充质干细胞标志物,并通过不对称和对称分化产生软骨细胞。细胞动力学的定量分析与磷钨酸增强型微计算机断层扫描相结合,表明表层细胞可产生软骨细胞,并有助于关节软骨的生长和重塑。此外,我们发现,在出生后早期,表层细胞的子代会完全取代胎儿软骨细胞,从而实现软骨更新。因此,表层细胞是自我更新的祖细胞,能够维持自身数量,并符合单能成体干细胞的标准。此外,这些细胞的子代可完全替代胎儿软骨细胞,从而重构成年关节软骨。-李,L.,牛顿,P.T.,布德里克,T.,塞伊诺霍娃,M.,齐克蒙德,T.,科热米亚基娜,E.,谢,M.,克里瓦内克,J.,凯泽,J.,钱,H.,迪亚丘克,V.,拉萨尔,A.B.,沃曼,M.L.,巴雷纽斯,B.,阿达梅伊科,I.,查金,A.S. 表层细胞是自我更新的软骨细胞祖细胞,在幼年小鼠中形成关节软骨