Single-cell transcriptomic analysis identifies extensive heterogeneity in the cellular composition of mouse Achilles tendons

肌腱 生物 跟腱 细胞外基质 细胞生物学 转录组 祖细胞 电池类型 细胞 干细胞 解剖 基因 计算生物学 遗传学 基因表达
作者
Andrea De Micheli,Jacob B. Swanson,Nathaniel P Disser,Leandro Marcelo Martinez,Nicholas R. Walker,David J. Oliver,Benjamin D. Cosgrove,Christopher L. Mendias
出处
期刊:American Journal of Physiology-cell Physiology [American Physical Society]
卷期号:319 (5): C885-C894 被引量:67
标识
DOI:10.1152/ajpcell.00372.2020
摘要

Tendon is a dense connective tissue that stores and transmits forces between muscles and bones. Cellular heterogeneity is increasingly recognized as an important factor in the biological basis of tissue homeostasis and disease, yet little is known about the diversity of cell types that populate tendon. To address this, we determined the heterogeneity of cell populations within mouse Achilles tendons using single-cell RNA sequencing. In assembling a transcriptomic atlas of Achilles tendons, we identified 11 distinct types of cells, including three previously undescribed populations of tendon fibroblasts. Prior studies have indicated that pericytes, which are found in the vasculature of tendons, could serve as a potential source of progenitor cells for adult tendon fibroblasts. Using trajectory inference analysis, we provide additional support for the notion that pericytes are likely to be at least one of the progenitor cell populations for the fibroblasts that compose adult tendons. We also modeled cell-cell interactions and identified previously undescribed ligand-receptor signaling interactions involved in tendon homeostasis. Our novel and interactive tendon atlas highlights previously underappreciated heterogeneity between and within tendon cell populations. The atlas also serves as a resource to further the understanding of tendon extracellular matrix assembly and maintenance and in the design of therapies for tendinopathies.
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