Evidence map›Paper›PMID 34895322›Full record

ArticleStem cell research & therapy2021

Bone marrow derived-mesenchymal stem cell improves diabetes-associated fatty liver via mitochondria transformation in mice.

Youkun Bi, Xuejun Guo, Mengqi Zhang, Keqi Zhu, Chentao Shi, Baoqi Fan, Yanyun Wu, Zhiguang Yang, Guangju Ji

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
10.5field-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

43 citing papers in PubMed, 87 citations in OpenAlex.

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  8. Nanomedicines Against Mitochondrial Dysfunction-Induced Metabolic Diseases.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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  11. MertkImmunity, inflammation and disease · 2025
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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

9 authors at 2 institutions in 1 country.

Youkun Bi *Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Xuejun Guo *Puyang Oilfield General Hospital, Affiliated to Xinxiang Medical College, Puyang city, 457000, Henan Province, China. pygxj@163.com.
Mengqi Zhang *Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Keqi ZhuInstitute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Chentao ShiPuyang Oilfield General Hospital, Affiliated to Xinxiang Medical College, Puyang city, 457000, Henan Province, China.
Baoqi FanInstitute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Yanyun WuInstitute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Zhiguang YangInstitute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Guangju JiInstitute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China. gj28@ibp.ac.cn.ORCID 0000-0001-8626-3490
Chinese Academy of Sciences · CNHenan Psychiatric Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-alcoholic fatty liver disease (NAFLD) has become a global epidemic disease. Its incidence is associated with type 2 diabetes mellitus (T2DM). Presently, there is no approved pharmacological agents specially developed for NAFLD. One promising disease-modifying strategy is the transplantation of stem cells to promote metabolic regulation and repair of injury.

methodIn this study, a T2DM model was established through 28-week high-fat diet (HFD) feeding resulting in T2DM-associated NAFLD, followed by the injection of bone marrow mesenchymal stem cells (BMSCs). The morphology, function, and transfer of hepatocyte mitochondria were evaluated in both vivo and in vitro.

resultsBMSC implantation resulted in the considerable recovery of increasing weight, HFD-induced steatosis, liver function, and disordered glucose and lipid metabolism. The treatment with BMSC transplantation was accompanied by reduced fat accumulation. Moreover, mitochondrial transfer was observed in both vivo and vitro studies. And the mitochondria-recipient steatotic cells exhibited significantly enhanced OXPHOS activity, ATP production, and mitochondrial membrane potential, and reduced reactive oxygen species levels, which were not achieved by the blocking of mitochondrial transfer.

conclusionMitochondrial transfer from BMSCs is a feasible process to combat NAFLD via rescuing dysfunction mitochondria, and has a promising therapeutic effect on metabolism-related diseases.

Indexed as

Diabetes Mellitus, Type 2Mesenchymal Stem CellsNon-alcoholic Fatty Liver DiseaseAnimalsBone MarrowDiet, High-FatLiverMiceMitochondriaBMSCsDiabetesMetabolismMitochondrialMitochondrial transferNAFLD

Identifiers

PMID34895322
PMCPMC8665517
OpenAlexW4200456992

What OpenQuestion holds

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Registered trials

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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.