Evidence map›Paper›PMID 32252818›Full record

ArticleStem cell research & therapy2020

Single-cell RNA-seq highlights heterogeneity in human primary Wharton's jelly mesenchymal stem/stromal cells cultured in vitro.

Changbin Sun, Lei Wang, Hailun Wang, Tingrun Huang, Wenwen Yao, Jing Li, Xi Zhang

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
10.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

69 citing papers in PubMed, 119 citations in OpenAlex.

  1. Review
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  3. Article
  4. Single-cell Technology in Stem Cell Research.Current stem cell research & therapy · 2025
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  11. Cell cycle expression heterogeneity predicts degree of differentiation.bioRxiv : the preprint server for biology · 2024
    Article
  12. Review
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  15. Review
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  17. Review
  18. Improved therapeutic consistency and efficacy of CD317Stem cell research & therapy · 2024
    Article
  19. Article
  20. Transplantation of the LRP1Stem cell research & therapy · 2024
    Article

9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Changbin SunBGI Education Center, University of Chinese Academy of Sciences, Shenzhen, 518083, China.
Lei WangBGI-Shenzhen, Shenzhen, 518083, China.
Hailun WangDepartment of Radiation Oncology, School of Medicine, Johns Hopkins University, Baltimore, MD, 21218, USA.
Tingrun HuangChina National GeneBank, BGI-Shenzhen, Shenzhen, 518120, China.
Wenwen YaoBGI-Shenzhen, Shenzhen, 518083, China.
Jing LiBGI-Shenzhen, Shenzhen, 518083, China.
Xi ZhangBGI-Shenzhen, Shenzhen, 518083, China. zhangxi1@genomics.cn.
BGI Group (China) · CNChina National GeneBank · CNJohns Hopkins University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMesenchymal stem/stromal cells (MSCs) are multipotent cells with a promising application potential in regenerative medicine and immunomodulation. However, MSCs cultured in vitro exhibit functional heterogeneity. The underlying molecular mechanisms that define MSC heterogeneity remain unclear.

methodsWe investigated the gene expression profile via single-cell RNA sequencing (scRNA-seq) of human primary Wharton's jelly-derived MSCs (WJMSCs) cultured in vitro from three donors. We also isolated CD142

resultsGO enrichment analysis of highly variable genes (HVGs) obtained from WJMSCs revealed that these genes are significantly enriched in extracellular region with binding function, involved in developmental process, signal transduction, cell proliferation, etc. Pathway analysis showed that these HVGs are associated with functional characteristics of classic MSCs, such as inflammation mediated by chemokine and cytokine signaling, integrin signaling, and angiogenesis. After regressing out the batch and cell cycle effects, these HVGs were used for dimension reduction and clustering analysis to identify candidate subpopulations. Differentially expressed gene analysis revealed the existence of several distinct subpopulations of MSCs that exhibit diverse functional characteristics related to proliferation, development, and inflammation response. In line with our data, sorted CD142

conclusionHVGs identified in MSCs are associated with classic MSC function. Regarding therapeutic potential, these genes are associated with functional characteristics, on which the MSC clinical application were theoretically based, such as development and inflammation response. Altogether, these HVGs hold the potential to be used as candidate markers for further potency association studies.

Indexed as

Mesenchymal Stem CellsWharton JellyCell DifferentiationCell ProliferationCells, CulturedHumansRNA-SeqUmbilical CordFunctional enrichmentHighly variable genesMSCsPotencyscRNA-seq

Identifiers

PMID32252818
PMCPMC7132901
OpenAlexW3015028387

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.