Evidence map›Paper›PMID 39010176›Full record

ArticleCell & bioscience2024

Generation of musculoskeletal cells from human urine epithelium-derived presomitic mesoderm cells.

Huiru Gao, Xingnan Huang, Zepo Cai, Baomei Cai, Kaipeng Wang, Junyang Li, Junqi Kuang, Bo Wang, Ziwei Zhai, Jin Ming and 3 more

Abstract read
In one paragraph

Article in Cell & bioscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Huiru Gao *CAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, 510530, China.
Xingnan Huang *Laboratory of Cell Fate Control, School of Life Sciences, Westlake University, Hangzhou, 310024, China.
Zepo CaiCAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, 510530, China.
Baomei CaiCAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, 510530, China.
Kaipeng WangLaboratory of Cell Fate Control, School of Life Sciences, Westlake University, Hangzhou, 310024, China.
Junyang LiLaboratory of Cell Fate Control, School of Life Sciences, Westlake University, Hangzhou, 310024, China.
Junqi KuangLaboratory of Cell Fate Control, School of Life Sciences, Westlake University, Hangzhou, 310024, China.
Bo WangLaboratory of Cell Fate Control, School of Life Sciences, Westlake University, Hangzhou, 310024, China.
Ziwei ZhaiCAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, 510530, China.
Jin MingLaboratory of Cell Fate Control, School of Life Sciences, Westlake University, Hangzhou, 310024, China.
Shangtao CaoGuangzhou Laboratory, Guangzhou, 510000, China.
Yue QinLaboratory of Cell Fate Control, School of Life Sciences, Westlake University, Hangzhou, 310024, China. qinyue@westlake.edu.cn.
Duanqing PeiLaboratory of Cell Fate Control, School of Life Sciences, Westlake University, Hangzhou, 310024, China. peiduanqing@westlake.edu.cn.

Funding

Key R&D Program of Zhejiang 2024SSYS0032National Natural Science Foundation of China 9206820National Natural Science Foundation Youth Foundation 32300672
6 · The paper itself

Abstract

backgroundNumerous studies have shown that somite development is a necessary stage of myogenesis chondrogenesis and osteogenesis. Our previous study has established a stable presomitic mesoderm progenitor cell line (UiPSM) in vitro. Naturally, we wanted to explore whether UiPSM cell can develop bone and myogenic differentiation.

resultsSelective culture conditions yielded PAX3 and PAX7 positive skeletal muscle precursors from UiPSM cells. The skeletal muscle precursors undergo in vitro maturation resulting in myotube formation. MYOD effectively promoted the maturity of the skeletal myocytes in a short time. We found that UiPSM and MYOD mediated UiPSM cell-derived skeletal myocytes were viable after transplantation into the tibialis anterior muscle of MITRG mice, as assessed by bioluminescence imaging and scRNA-seq. Lack of teratoma formation and evidence of long-term myocytes engraftment suggests considerable potential for future therapeutic applications. Moreover, UiPSM cells can differentiate into osteoblast and chondroblast cells in vitro.

conclusionsUiPSM differentiation has potential as a developmental model for musculoskeletal development research and treatment of musculoskeletal disorders.

Indexed as

DifferentiationMYODSkeletal myocytesTransplantationUiPSM cell

Identifiers

PMID39010176
PMCPMC11251367

What Socratic 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 Socratic graph.