诱导多能干细胞
软骨细胞
软骨
药物发现
疾病
神经科学
干细胞
人诱导多能干细胞
计算生物学
医学
生物
生物信息学
细胞生物学
病理
胚胎干细胞
解剖
遗传学
基因
作者
Pauline De Kinderen,Josephina Meester,Bart Loeys,Silke Peeters,Elvire Gouze,Steven Paul Woods,Geert Mortier,Aline Verstraeten
摘要
ABSTRACT Induced pluripotent stem cell (iPSC) technology allows pathomechanistic and therapeutic investigation of human heritable disorders affecting tissue types whose collection from patients is difficult or even impossible. Among them are cartilage diseases. Over the past decade, iPSC-chondrocyte disease models have been shown to exhibit several key aspects of known disease mechanisms. Concurrently, an increasing number of protocols to differentiate iPSCs into chondrocytes have been published, each with its respective (dis)advantages. In this review we provide a comprehensive overview of the different differentiation approaches, the hitherto described iPSC-chondrocyte disease models and mechanistic and/or therapeutic insights that have been derived from their investigation, and the current model limitations. Key lessons are that the most appropriate differentiation approach is dependent upon the cartilage disease under investigation and that further optimization is still required to recapitulate the in vivo cartilage. © 2022 American Society for Bone and Mineral Research (ASBMR).
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