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间充质干细胞异质性及其分化潜能的跨组织特征分析

Cross-Tissue Characterization of Heterogeneities of Mesenchymal Stem Cells and Their Differentiation Potentials.

作者信息

Hou Wenhong, Duan Li, Huang Changyuan, Li Xingfu, Xu Xiao, Qin Pengfei, Hong Ni, Wang Daping, Jin Wenfei

机构信息

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.

出版信息

Front Cell Dev Biol. 2021 Dec 17;9:781021. doi: 10.3389/fcell.2021.781021. eCollection 2021.


DOI:10.3389/fcell.2021.781021
PMID:34977025
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8719164/
Abstract

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.

摘要

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。

相似文献

[1]
Cross-Tissue Characterization of Heterogeneities of Mesenchymal Stem Cells and Their Differentiation Potentials.

Front Cell Dev Biol. 2021-12-17

[2]
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[3]
Tissue source determines the differentiation potentials of mesenchymal stem cells: a comparative study of human mesenchymal stem cells from bone marrow and adipose tissue.

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[4]
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[5]
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[6]
Adipogenic potentials of mesenchymal stem cells from human bone marrow, umbilical cord and adipose tissue are different.

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2014-6

[7]
IL-17A and TNF Modulate Normal Human Spinal Entheseal Bone and Soft Tissue Mesenchymal Stem Cell Osteogenesis, Adipogenesis, and Stromal Function.

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[8]
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[9]
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Am J Sports Med. 2017-9

[10]
Differential expression of cell cycle and WNT pathway-related genes accounts for differences in the growth and differentiation potential of Wharton's jelly and bone marrow-derived mesenchymal stem cells.

Stem Cell Res Ther. 2017-4-26

引用本文的文献

[1]
Combining transcriptomic and metabolomic insights to guide the clinical application of adipose- and bone marrow-derived mesenchymal stem cells.

Med Rev (2021). 2024-8-29

[2]
Single-cell transcriptomic analysis of chondrocytes in cartilage and pathogenesis of osteoarthritis.

Genes Dis. 2024-2-2

[3]
Human Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes Loaded Mir-29-3p Targets AhR to Improve Juvenile Idiopathic Arthritis via Inhibiting the Expression of IL-22 in CD4 T Cell.

Stem Cell Rev Rep. 2025-2

[4]
N-CADHERIN/CD168 subpopulation determines therapeutic variations of UC-MSCs for cardiac repair after myocardial infarction.

Stem Cell Res Ther. 2024-11-13

[5]
Engineering mesenchymal stem cells for premature ovarian failure: overcoming challenges and innovating therapeutic strategies.

Theranostics. 2024

[6]
The issue of heterogeneity of MSC-based advanced therapy medicinal products-a review.

Front Cell Dev Biol. 2024-7-26

[7]
Comparison studies identify mesenchymal stromal cells with potent regenerative activity in osteoarthritis treatment.

NPJ Regen Med. 2024-4-1

[8]
Unveiling the functional heterogeneity of cytokine-primed human umbilical cord mesenchymal stem cells through single-cell RNA sequencing.

Cell Biosci. 2024-3-26

[9]
Comparative transcriptomic analysis of bovine mesenchymal stromal cells reveals tissue-source and species-specific differences.

iScience. 2024-1-12

[10]
Application progress of single-cell sequencing technology in mesenchymal stem cells research.

Front Cell Dev Biol. 2024-1-9

本文引用的文献

[1]
A plate-based single-cell ATAC-seq workflow for fast and robust profiling of chromatin accessibility.

Nat Protoc. 2021-8

[2]
Integrated decoding hematopoiesis and leukemogenesis using single-cell sequencing and its medical implication.

Cell Discov. 2021-1-5

[3]
Visualization of Single Cell RNA-Seq Data Using t-SNE in R.

Methods Mol Biol. 2020

[4]
Exploring the changing landscape of cell-to-cell variation after CTCF knockdown via single cell RNA-seq.

BMC Genomics. 2019-12-26

[5]
Combined single-cell and spatial transcriptomics reveal the molecular, cellular and spatial bone marrow niche organization.

Nat Cell Biol. 2019-12-23

[6]
Cell-to-Cell Culture Inhibits Dedifferentiation of Chondrocytes and Induces Differentiation of Human Umbilical Cord-Derived Mesenchymal Stem Cells.

Biomed Res Int. 2019-11-16

[7]
Single-Cell Signature Explorer for comprehensive visualization of single cell signatures across scRNA-seq datasets.

Nucleic Acids Res. 2019-12-2

[8]
Mapping Distinct Bone Marrow Niche Populations and Their Differentiation Paths.

Cell Rep. 2019-7-9

[9]
Single cell transcriptomic analysis of human mesenchymal stem cells reveals limited heterogeneity.

Cell Death Dis. 2019-5-8

[10]
Identification of a mesenchymal progenitor cell hierarchy in adipose tissue.

Science. 2019-4-26

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