Evidence map›Paper›PMID 35922833›Full record

ArticleStem cell research & therapy2022

Irisin enhances chondrogenic differentiation of human mesenchymal stem cells via Rap1/PI3K/AKT axis.

Taiqiu Chen, Yan Peng, Wenjun Hu, Huihong Shi, Pengfei Li, Yichen Que, Jincheng Qiu, Xianjian Qiu, Bo Gao, Hang Zhou and 6 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. The characteristic expression of circulatingFrontiers in endocrinology · 2024
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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

16 authors at 1 institution in 1 country.

Taiqiu Chen *Department of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Yan Peng *Department of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Wenjun Hu *Department of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Huihong ShiDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Pengfei LiDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Yichen QueDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Jincheng QiuDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Xianjian QiuDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Bo GaoDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Hang ZhouDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Yanbo ChenDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Yuanxin ZhuDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Shaoguang LiDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Anjing LiangDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China.
Wenjie GaoDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China. gaowj7@mail.sysu.edu.cn.ORCID 0000-0001-9456-8884
Dongsheng HuangDepartment of Orthopedics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, #107 West Yan Jiang Road, Guangzhou, Guangdong, China. hdongsh@mail.sysu.edu.cn.
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman mesenchymal stem cells (hMSCs) have been proven to have inherent chondrogenic differentiation potential, which appears to be used in cartilage regeneration. Increasing evidence suggests that irisin enhances osteoblast differentiation of MSCs, but little is known about its potential on chondrogenic differentiation.

methodsIn the study, we investigated the effects of irisin on chondrogenic differentiation of hMSCs using a high-density pellet culture system. The cartilage pellets were evaluated by morphology, and the metabolism of cartilage matrix was detected by qPCR, western blot and immunohistochemistry. Next, RNA-seq was performed to explore the underlying mechanism. Furthermore, using the transduction of plasmid, miRNAs mimics and inhibitor, the activation of Rap1/PI3K/AKT axis, the expression level of SIPA1L2, and the functional verification of miR-125b-5p were detected on day 7 of chondrogenic differentiation of hMSCs.

resultsCompared with the controls, we found that irisin treatment could significantly enhance the chondrogenic differentiation of hMSCs, enlarge the induced-cartilage tissue and up-regulate the expression levels of cartilage markers. RNA-seq indicated that irisin activated the Rap1 and PI3K/AKT signaling pathway, and the lower expression level of SIPA1L2 and the higher expression level of miR-125b-5p were found in irisin-treated group. Further, we found that irisin treatment could up-regulate the expression level of miR-125b-5p, targeting SIPA1L2 and consequently activating the Rap1/PI3K/AKT axis on the process of chondrogenic differentiation of hMSCs.

conclusionsCollectively, our study reveals that irisin can enhance chondrogenic differentiation of hMSCs via the Rap1/PI3K/AKT pathway, suggesting that irisin possesses prospects in cartilage regeneration.

Indexed as

Mesenchymal Stem CellsMicroRNAsCells, CulturedFibronectinsHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktrap1 GTP-Binding ProteinsFibronectinsMicroRNAsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktrap1 GTP-Binding ProteinsChondrogenic differentiationHuman mesenchymal stem cellsIrisinmiR-125b-5pRap1/PI3K/AKT signaling pathwaySIPA1L2

Identifiers

PMID35922833
PMCPMC9351134
OpenAlexW4289549827

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.