Single‐Cell and Spatial Transcriptomics Decodes Wharton's Jelly‐Derived Mesenchymal Stem Cells Heterogeneity and a Subpopulation with Wound Repair Signatures. Issue 4 (11th December 2022)
- Record Type:
- Journal Article
- Title:
- Single‐Cell and Spatial Transcriptomics Decodes Wharton's Jelly‐Derived Mesenchymal Stem Cells Heterogeneity and a Subpopulation with Wound Repair Signatures. Issue 4 (11th December 2022)
- Main Title:
- Single‐Cell and Spatial Transcriptomics Decodes Wharton's Jelly‐Derived Mesenchymal Stem Cells Heterogeneity and a Subpopulation with Wound Repair Signatures
- Authors:
- Chen, Penghong
Tang, Shijie
Li, Ming
Wang, Dezhi
Chen, Caixiang
Qiu, Yiqun
Fang, Zhuoqun
Zhang, Haoruo
Gao, Hangqi
Weng, Haiyan
Hu, Kailun
Lin, Jian
Lin, Qingxia
Tan, Yi
Li, Shirong
Chen, Jinghua
Chen, Liangwan
Chen, Xiaosong - Abstract:
- Abstract: The highly heterogeneous characteristics of Wharton's jelly mesenchymal stem cells (WJ‐MSCs) may be responsible for the poor clinical outcomes and poor reproducibility of treatments based on WJ‐MSCs. Exploration of WJ‐MSC heterogeneity with multimodal single‐cell technologies will aid in establishing accurate MSC subtyping and developing screening protocols for dominant functional subpopulations. Here, the characteristics of WJ‐MSCs are systematically analyzed by single cell and spatial transcriptome sequencing. Single‐cell transcriptomics analysis identifies four WJ‐MSC subpopulations, namely proliferative_MSCs, niche‐supporting_MSCs, metabolism‐related_MSCs and biofunctional‐type_MSCs. Furthermore, the transcriptome, cellular heterogeneity, and cell‐state trajectories of these subpopulations are characterized. Intriguingly, the biofunctional‐type MSCs (marked by S100A9, CD29, and CD142) selected in this study exhibit promising wound repair properties in vitro and in vivo. Finally, by integrating omics data, it has been found that the S100A9 + CD29 + CD142 + subpopulation is more enriched in the fetal segment of the umbilical cord, suggesting that this subpopulation deriving from the fetal segment may have potential for developing into an ideal therapeutic agent for wound healing. Overall, the presented study comprehensively maps the heterogeneity of WJ‐MSCs and provides an essential resource for future development of WJ‐MSC‐based drugs. Abstract : TheAbstract: The highly heterogeneous characteristics of Wharton's jelly mesenchymal stem cells (WJ‐MSCs) may be responsible for the poor clinical outcomes and poor reproducibility of treatments based on WJ‐MSCs. Exploration of WJ‐MSC heterogeneity with multimodal single‐cell technologies will aid in establishing accurate MSC subtyping and developing screening protocols for dominant functional subpopulations. Here, the characteristics of WJ‐MSCs are systematically analyzed by single cell and spatial transcriptome sequencing. Single‐cell transcriptomics analysis identifies four WJ‐MSC subpopulations, namely proliferative_MSCs, niche‐supporting_MSCs, metabolism‐related_MSCs and biofunctional‐type_MSCs. Furthermore, the transcriptome, cellular heterogeneity, and cell‐state trajectories of these subpopulations are characterized. Intriguingly, the biofunctional‐type MSCs (marked by S100A9, CD29, and CD142) selected in this study exhibit promising wound repair properties in vitro and in vivo. Finally, by integrating omics data, it has been found that the S100A9 + CD29 + CD142 + subpopulation is more enriched in the fetal segment of the umbilical cord, suggesting that this subpopulation deriving from the fetal segment may have potential for developing into an ideal therapeutic agent for wound healing. Overall, the presented study comprehensively maps the heterogeneity of WJ‐MSCs and provides an essential resource for future development of WJ‐MSC‐based drugs. Abstract : The heterogeneity of Wharton's jelly mesenchymal stem cells (WJ‐MSCs) hampers clinical translation. The authors map a comprehensive single‐cell and spatial transcriptomic atlas to decipher the heterogeneity of WJ‐MSCs, and verify the efficient wound repair capabilities of the S100A9 + CD29 + CD142 + subpopulations, which are more enriched in the fetal segment of an umbilical cord, providing a more targeted way to treat diseases. … (more)
- Is Part Of:
- Advanced science. Volume 10:Issue 4(2023)
- Journal:
- Advanced science
- Issue:
- Volume 10:Issue 4(2023)
- Issue Display:
- Volume 10, Issue 4 (2023)
- Year:
- 2023
- Volume:
- 10
- Issue:
- 4
- Issue Sort Value:
- 2023-0010-0004-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-12-11
- Subjects:
- heterogeneity -- single‐cell RNA sequencing -- spatial transcriptome -- subpopulations -- Wharton's jelly‐derived mesenchymal stem cells
Science -- Periodicals
505 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2198-3844 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/advs.202204786 ↗
- Languages:
- English
- ISSNs:
- 2198-3844
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25717.xml