Evidence map›Paper›PMID 40052924›Full record

ArticleThe Journal of cell biology2025

SNX10 functions as a modulator of piecemeal mitophagy and mitochondrial bioenergetics.

Laura Trachsel-Moncho, Chiara Veroni, Benan John Mathai, Ana Lapao, Sakshi Singh, Nagham Theres Asp, Sebastian W Schultz, Serhiy Pankiv, Anne Simonsen

Abstract read
In one paragraph

Article in The Journal of cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Regulation and roles of mammalian mitophagy.Nature reviews. Molecular cell biology · 2026
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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.

Laura Trachsel-MonchoDepartment of Molecular Medicine, Institute of Basic Medical Sciences Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0002-8525-7790
Chiara Veroni *Department of Molecular Medicine, Institute of Basic Medical Sciences Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0009-0009-0348-0672
Benan John Mathai *Department of Molecular Medicine, Institute of Basic Medical Sciences Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0002-9549-2073
Ana LapaoDepartment of Molecular Medicine, Institute of Basic Medical Sciences Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0002-5816-1240
Sakshi SinghDepartment of Molecular Medicine, Institute of Basic Medical Sciences Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0002-2168-1066
Nagham Theres AspDepartment of Molecular Medicine, Institute of Basic Medical Sciences Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0002-2143-1470
Sebastian W SchultzCenter for Cancer Cell Reprogramming, Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0002-3661-2178
Serhiy PankivDepartment of Molecular Medicine, Institute of Basic Medical Sciences Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0001-7953-2445
Anne SimonsenDepartment of Molecular Medicine, Institute of Basic Medical Sciences Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0003-4711-7057

Funding

Marie Skłodowska-Curie 801133Norwegian Cancer Society 171318Research Council of Norway 295910South-Eastern Norway Regional Health AuthoritySouth-Eastern Norway Regional Health Authority 2020032University of Oslo
6 · The paper itself

Abstract

We here identify the endosomal protein SNX10 as a negative regulator of piecemeal mitophagy of OXPHOS machinery components. In control conditions, SNX10 localizes to early endocytic compartments in a PtdIns3P-dependent manner and modulates endosomal trafficking but also shows dynamic connections with mitochondria. Upon hypoxia-mimicking conditions, SNX10 localizes to late endosomal structures containing selected mitochondrial proteins, including COX-IV and SAMM50, and the autophagy proteins SQSTM1/p62 and LC3B. The turnover of COX-IV was enhanced in SNX10-depleted cells, with a corresponding reduced mitochondrial respiration and citrate synthase activity. Importantly, zebrafish larvae lacking Snx10 show reduced levels of Cox-IV, as well as elevated ROS levels and ROS-mediated cell death in the brain, demonstrating the in vivo relevance of SNX10-mediated modulation of mitochondrial bioenergetics.

Indexed as

Energy MetabolismMitochondriaMitophagySorting NexinsZebrafish ProteinsAnimalsEndosomesHeLa CellsHumansOxidative PhosphorylationReactive Oxygen SpeciesZebrafishReactive Oxygen SpeciesSNX10 protein, humanSorting NexinsZebrafish Proteins

Identifiers

PMID40052924
PMCPMC11893173

What OpenQuestion holds

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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 OpenQuestion graph.