类有机物
生物
诱导多能干细胞
干细胞
细胞生物学
人诱导多能干细胞
胚胎干细胞
遗传学
基因
作者
Yin Yao,Wei Zhou,Jinkui Zhu,Ziling Chen,Linlin Jiang,Xuran Zhuang,Jia Chen,Jianfeng Wei,Xiaoxiang Lu,Yantong Liu,Wei Pang,Qingguang Zhang,Yingze Cao,Zhuoya Li,Yuyan Zhu,Yangfei Xiang
标识
DOI:10.1016/j.stem.2024.11.005
摘要
The human body function requires crosstalk between different tissues. An essential crosstalk is in the neuromusculoskeletal (NMS) axis involving neural, muscular, and skeletal tissues, which is challenging to model using human cells. Here, we describe the generation of three-dimensional, NMS tri-tissue organoids (hNMSOs) from human pluripotent stem cells through a co-development strategy. Staining, single-nucleus RNA sequencing, and spatial transcriptome profiling revealed the co-emergence and self-organization of neural, muscular, and skeletal lineages within individual organoids, and the neural domains of hNMSOs obtained a ventral-specific identity and produced motor neurons innervating skeletal muscles. The neural, muscular, and skeletal regions of hNMSOs exhibited maturation and established functional connections during development. Notably, structural, functional, and transcriptomic analyses revealed that skeletal support in hNMSOs benefited human muscular development. Modeling with hNMSOs also unveiled the neuromuscular alterations following pathological skeletal degeneration. Together, our study provides an accessible experimental model for future studies of human NMS crosstalk and abnormality.
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