Evidence map›Paper›PMID 40289989›Full record

ReviewCurrent stem cell research & therapy2025

Mitochondria Transfer in Mesenchymal Stem Cells: Unraveling the Mechanism and Therapeutic Potential.

Jingyi Chen, Zhilang Xie, Huayin Zhou, Yingxin Ou, Wenwen Tan, Aizhen Zhang, Yuying Li, Xingliang Fan

Abstract readReview
In one paragraph

Review in Current stem cell research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Thyroid hormones, mitochondria, aging, and cancer.Frontiers in endocrinology · 2025
    Review
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

8 authors.

Jingyi ChenInstitute of Biological and Food Engineering, Guangdong University of Education, 351 Xingang Middle Road, Guangzhou, 510303, P.R. China.
Zhilang XieInstitute of Biological and Food Engineering, Guangdong University of Education, 351 Xingang Middle Road, Guangzhou, 510303, P.R. China.
Huayin ZhouInstitute of Biological and Food Engineering, Guangdong University of Education, 351 Xingang Middle Road, Guangzhou, 510303, P.R. China.
Yingxin OuInstitute of Biological and Food Engineering, Guangdong University of Education, 351 Xingang Middle Road, Guangzhou, 510303, P.R. China.
Wenwen TanInstitute of Biological and Food Engineering, Guangdong University of Education, 351 Xingang Middle Road, Guangzhou, 510303, P.R. China.
Aizhen ZhangInstitute of Biological and Food Engineering, Guangdong University of Education, 351 Xingang Middle Road, Guangzhou, 510303, P.R. China.
Yuying LiInstitute of Biological and Food Engineering, Guangdong University of Education, 351 Xingang Middle Road, Guangzhou, 510303, P.R. China.
Xingliang FanInstitute of Biological and Food Engineering, Guangdong University of Education, 351 Xingang Middle Road, Guangzhou, 510303, P.R. China.ORCID 0000-0002-8902-8389

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) hold transformative potential in translational medicine due to their versatile differentiation abilities and regenerative properties. Notably, MSCs can transfer mitochondria to unrelated cells through intercellular mitochondrial transfer, offering a groundbreaking approach to halting the progression of mitochondrial diseases and restoring function to cells compromised by mitochondrial dysfunction. Although MSC mitochondrial transfer has demonstrated significant therapeutic promise across a range of diseases, its application in clinical settings remains largely unexplored. This review delves into the novel mechanisms by which MSCs execute mitochondrial transfer, highlighting its profound impact on cellular metabolism, immune modulation, and tissue regeneration. We provide an in-depth analysis of the therapeutic potential of MSC mitochondrial transfer, particularly in treating mitochondrial dysfunction-related diseases and advancing tissue repair strategies. Additionally, we propose innovative considerations for optimizing MSC mitochondrial transfer in clinical trials, emphasizing its potential to reshape the landscape of regenerative medicine and therapeutic interventions.

Indexed as

Mesenchymal Stem CellsMesenchymal Stem Cell TransplantationMitochondriaMitochondrial DiseasesAnimalsCell DifferentiationHumansRegenerative Medicinecell apoptosis.extracellular vesiclesimmunomodulationMesenchymal stem cellsmitochondrial transferoxidative stresstherapeutic potentialtunneling nanotubes

Identifiers

PMID40289989
PMCPMC12728536

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.