Evidence map›Paper›PMID 39133213›Full record

ArticleThe Journal of cell biology2024

Dynamic interaction of REEP5-MFN1/2 enables mitochondrial hitchhiking on tubular ER.

Shue Chen, Yang Sun, Yuling Qin, Lan Yang, Zhenhua Hao, Zhihao Xu, Mikael Björklund, Wei Liu, Zhi Hong

Abstract read
In one paragraph

Article in The Journal of cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. ATL2 Recruits TRAK1 to Promote Mitochondrial Transport at ER-Mitochondria Contact Sites.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. 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

9 authors.

Shue Chen *Department of Neurology, the Second Affiliated Hospital of Zhejiang University, School of Medicine, Zhejiang University, Hangzhou, China.ORCID 0000-0002-0061-8041
Yang Sun *Department of Neurology, the Second Affiliated Hospital of Zhejiang University, School of Medicine, Zhejiang University, Hangzhou, China.ORCID 0009-0009-4148-5386
Yuling QinDepartment of Neurology, the Second Affiliated Hospital of Zhejiang University, School of Medicine, Zhejiang University, Hangzhou, China.ORCID 0009-0006-5250-064X
Lan YangDepartment of Neurology, the Second Affiliated Hospital of Zhejiang University, School of Medicine, Zhejiang University, Hangzhou, China.ORCID 0009-0002-5649-6044
Zhenhua HaoNational Center for Children's Health, Beijing Children's Hospital, Capital Medical University, Beijing, China.ORCID 0000-0002-2275-1927
Zhihao XuDepartment of Neurology, the Second Affiliated Hospital of Zhejiang University, School of Medicine, Zhejiang University, Hangzhou, China.ORCID 0009-0001-2468-7009
Mikael BjörklundCentre for Cellular Biology and Signaling, Zhejiang University-University of Edinburgh Institute, Haining, China.ORCID 0000-0002-2176-681X
Wei LiuMetabolic Medicine Center, International Institutes of Medicine, the Fourth Affiliated Hospital, School of Medicine, Zhejiang University, Yiwu, China.ORCID 0000-0002-8033-4718
Zhi HongDepartment of Neurology, the Second Affiliated Hospital of Zhejiang University, School of Medicine, Zhejiang University, Hangzhou, China.ORCID 0009-0003-8977-9486

Funding

National Natural Science Foundation of China 32070700
6 · The paper itself

Abstract

Mitochondrial functions can be regulated by membrane contact sites with the endoplasmic reticulum (ER). These mitochondria-ER contact sites (MERCs) are functionally heterogeneous and maintained by various tethers. Here, we found that REEP5, an ER tubule-shaping protein, interacts with Mitofusins 1/2 to mediate mitochondrial distribution throughout the cytosol by a new transport mechanism, mitochondrial "hitchhiking" with tubular ER on microtubules. REEP5 depletion led to reduced tethering and increased perinuclear localization of mitochondria. Conversely, increasing REEP5 expression facilitated mitochondrial distribution throughout the cytoplasm. Rapamycin-induced irreversible REEP5-MFN1/2 interaction led to mitochondrial hyperfusion, implying that the dynamic release of mitochondria from tethering is necessary for normal mitochondrial distribution and dynamics. Functionally, disruption of MFN2-REEP5 interaction dynamics by forced dimerization or silencing REEP5 modulated the production of mitochondrial reactive oxygen species (ROS). Overall, our results indicate that dynamic REEP5-MFN1/2 interaction mediates cytosolic distribution and connectivity of the mitochondrial network by "hitchhiking" and this process regulates mitochondrial ROS, which is vital for multiple physiological functions.

Indexed as

Endoplasmic ReticulumGTP PhosphohydrolasesMitochondriaReactive Oxygen SpeciesCytosolHEK293 CellsHeLa CellsHumansMicrotubulesMitochondrial DynamicsMitochondrial Membrane Transport ProteinsMitochondrial ProteinsProtein BindingGTP PhosphohydrolasesMfn1 protein, humanMFN2 protein, humanMitochondrial Membrane Transport ProteinsMitochondrial ProteinsReactive Oxygen Species

Identifiers

PMID39133213
PMCPMC11318672

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.