Hou Wenhong, Duan Li, Huang Changyuan, Li Xingfu, Xu Xiao, Qin Pengfei, Hong Ni, Wang Daping, Jin Wenfei
Shenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen, China.
Department of Orthopedics, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, China.
Front Cell Dev Biol. 2021 Dec 17;9:781021. doi: 10.3389/fcell.2021.781021. eCollection 2021.
Mesenchymal stem/stromal cells (MSCs) are promising cell sources for regenerative medicine and the treatment of autoimmune disorders. Comparing MSCs from different tissues at the single-cell level is fundamental for optimizing clinical applications. Here we analyzed single-cell RNA-seq data of MSCs from four tissues, namely umbilical cord, bone marrow, synovial tissue, and adipose tissue. We identified three major cell subpopulations, namely osteo-MSCs, chondro-MSCs, and adipo/myo-MSCs, across all MSC samples. MSCs from the umbilical cord exhibited the highest immunosuppression, potentially indicating it is the best immune modulator for autoimmune diseases. MSC subpopulations, with different subtypes and tissue sources, showed pronounced differences in differentiation potentials. After we compared the cell subpopulations and cell status pre-and-post chondrogenesis induction, osteogenesis induction, and adipogenesis induction, respectively, we found MSC subpopulations expanded and differentiated when their subtypes consist with induction directions, while the other subpopulations shrank. We identified the genes and transcription factors underlying each induction at the single-cell level and subpopulation level, providing better targets for improving induction efficiency.
间充质干/基质细胞(MSCs)是再生医学和自身免疫性疾病治疗中很有前景的细胞来源。在单细胞水平上比较不同组织来源的MSCs对于优化临床应用至关重要。在此,我们分析了来自脐带、骨髓、滑膜组织和脂肪组织这四种组织的MSCs的单细胞RNA测序数据。我们在所有MSC样本中鉴定出三个主要细胞亚群,即骨源性MSCs、软骨源性MSCs和脂肪/肌源性MSCs。脐带来源的MSCs表现出最强的免疫抑制作用,这可能表明它是自身免疫性疾病的最佳免疫调节剂。不同亚型和组织来源的MSC亚群在分化潜能上表现出明显差异。在分别比较软骨形成诱导、成骨诱导和脂肪形成诱导前后的细胞亚群和细胞状态后,我们发现当MSC亚群的亚型与诱导方向一致时,它们会扩增并分化,而其他亚群则会缩小。我们在单细胞水平和亚群水平上鉴定了每种诱导过程背后的基因和转录因子,为提高诱导效率提供了更好的靶点。
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