Evidence map›Paper›PMID 41340078›Full record

SynthesisEuropean journal of medical research2025

Mitochondrial dynamics and function in neural differentiation: a systematic review.

Arman Armat, Arash Pooladi, Seyedeh Asrin Seyedoshohadaei, Borhan Moradveisi, Maedeh Khanyabzadeh, Shaho Badri, Ramyar Rahimi Darehbagh

Abstract readSystematic Review
In one paragraph

Synthesis in European journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

7 authors.

Arman ArmatStudent Research Committee, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Arash PooladiCancer and Immunology Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Seyedeh Asrin SeyedoshohadaeiNeurosciences Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Borhan MoradveisiPediatric Hematologist-Oncologist, Professor Associated, Cancer and Immunology Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Maedeh KhanyabzadehStudent Research Committee, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Shaho BadriStudent Research Committee, Kurdistan University of Medical Sciences, P.O.Box, SanandajSanandaj, 66135-756, Iran.
Ramyar Rahimi DarehbaghStudent Research Committee, Kurdistan University of Medical Sciences, P.O.Box, SanandajSanandaj, 66135-756, Iran. ramyar.rahimi@yahoo.com.ORCID http://orcid.org/0000-0003-4494-4380

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMitochondrial function has emerged as a critical regulator of neural differentiation, yet a comprehensive understanding of its diverse roles and temporal dynamics remains elusive. This systematic review synthesizes current evidence regarding mitochondrial contributions to neural stem cell differentiation and their implications for neurodevelopmental disorders.

methodsA systematic search was conducted across PubMed, Web of Science, and Scopus databases from inception to January 2025. Studies investigating mitochondrial properties during neural differentiation were included. Data extraction focused on temporal changes in mitochondrial function, molecular mechanisms, and pathological implications. Quality assessment was performed using modified SYRCLE criteria.

resultsAnalysis of 50 studies revealed distinct temporal patterns of mitochondrial regulation during neural differentiation. Early stages (days 0-3) showed predominant mitochondrial fragmentation and elevated ROS levels, while intermediate stages (days 4-7) demonstrated a shift toward oxidative phosphorylation with increased fusion events. Late-stage differentiation (beyond day 7) exhibited mature mitochondrial networks and stable bioenergetic profiles. The key molecular mechanisms included calcium signaling, Wnt/β-catenin pathway activation, and dynamic regulation of fusion/fission proteins. Mitochondrial dysfunction was consistently associated with impaired neural differentiation across multiple neurodevelopmental disorders.

conclusionsMitochondrial regulation of neural differentiation involves stage-specific changes in morphology, metabolism, and signaling functions. The identification of key molecular pathways provides promising therapeutic targets for neurodevelopmental disorders. Future research should focus on standardizing assessment methods, understanding tissue-specific regulation, and developing targeted interventions for clinical applications. These findings highlight the therapeutic potential of mitochondrial-targeted approaches in treating neurodevelopmental disorders and advancing regenerative medicine strategies.

Indexed as

Cell DifferentiationMitochondriaMitochondrial DynamicsNeural Stem CellsNeurodevelopmental DisordersNeurogenesisAnimalsHumansMitochondriaMitochondrial dynamicsNeural differentiationNeural stem cellsNeurodevelopmentSystematic review

Identifiers

PMID41340078
PMCPMC12676760

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.