Evidence map›Paper›PMID 38547062›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Force-induced tail-autotomy mitochondrial fission and biogenesis of matrix-excluded mitochondrial-derived vesicles for quality control.

Xiaoying Liu, Linyu Xu, Yutong Song, Zhihao Zhao, Xinyu Li, Cheuk-Yiu Wong, Rong Chen, Jianxiong Feng, Yitao Gou, Yajing Qi and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 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
4.0field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

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  12. Light-Inducible Deformation of Mitochondria in Live Cells.Methods in molecular biology (Clifton, N.J.) · 2025
    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

16 authors at 3 institutions in 2 countries.

Xiaoying LiuDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.ORCID 0000-0002-2301-0207
Linyu XuDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.ORCID 0009-0002-7891-7559
Yutong SongDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.
Zhihao ZhaoDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.
Xinyu LiDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.
Cheuk-Yiu WongDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.
Rong ChenDepartment of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Hong Kong SAR 999077, China.
Jianxiong FengState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou 510060, China.
Yitao GouDepartment of Physics, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.
Yajing QiDepartment of Physics, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.ORCID 0009-0008-0411-6488
Hei-Man ChowSchool of Life Sciences, Faculty of Science, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.ORCID 0000-0003-1203-2096
Shuhuai YaoDepartment of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Hong Kong SAR 999077, China.
Yi WangDepartment of Physics, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.ORCID 0000-0002-4174-8790
Song GaoState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou 510060, China.
Xingguo LiuChinese Academy of Sciences Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, China-New Zealand Joint Laboratory on Biomedicine and Health, Chinese University of Hong Kong-Guangzhou Institutes of Biomedicine and Health (CUHK-GIBH) Joint Research Laboratory on Stem Cells and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou Medical University, Guangzhou 510000, China.
Liting DuanDepartment of Biomedical Engineering, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.ORCID 0000-0001-8978-8890
Chinese University of Hong Kong · HKHong Kong University of Science and Technology · HKSun Yat-sen University · CN

Funding

MOST | National Key Research and Development Program of China (NKPs) 2021YFA0910700
6 · The paper itself

Abstract

Mitochondria constantly fuse and divide for mitochondrial inheritance and functions. Here, we identified a distinct type of naturally occurring fission, tail-autotomy fission, wherein a tail-like thin tubule protrudes from the mitochondrial body and disconnects, resembling autotomy. Next, utilizing an optogenetic mitochondria-specific mechanostimulator, we revealed that mechanical tensile force drives tail-autotomy fission. This force-induced fission involves DRP1/MFF and endoplasmic reticulum tubule wrapping. It redistributes mitochondrial DNA, producing mitochondrial fragments with or without mitochondrial DNA for different fates. Moreover, tensile force can decouple outer and inner mitochondrial membranes, pulling out matrix-excluded tubule segments. Subsequent tail-autotomy fission separates the matrix-excluded tubule segments into matrix-excluded mitochondrial-derived vesicles (MDVs) which recruit Parkin and LC3B, indicating the unique role of tail-autotomy fission in segregating only outer membrane components for mitophagy. Sustained force promotes fission and MDV biogenesis more effectively than transient one. Our results uncover a mechanistically and functionally distinct type of fission and unveil the role of tensile forces in modulating fission and MDV biogenesis for quality control, underscoring the heterogeneity of fission and mechanoregulation of mitochondrial dynamics.

Indexed as

Membrane ProteinsMitochondrial DynamicsDNA, MitochondrialDynaminsMitochondriaMitochondrial ProteinsQuality ControlDNA, MitochondrialDynaminsMembrane ProteinsMitochondrial Proteinsmitochondrial fissionmitochondrial quality controloptogeneticsphotoactivatable proteinstensile force

Identifiers

PMID38547062
PMCPMC10998583
OpenAlexW4393254560

What OpenQuestion 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 OpenQuestion graph.