Evidence map›Paper›PMID 39136939›Full record

ArticleThe Journal of cell biology2024

Mitochondrial-derived compartments are multilamellar domains that encase membrane cargo and cytosol.

Zachary N Wilson, Matt West, Alyssa M English, Greg Odorizzi, Adam L Hughes

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. Mitochondrial localization of key NADApplied and environmental microbiology · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Rab14 promotes Parkin-mediated mitophagy.Molecular biology of the cell · 2025
    Article
  8. Mechanisms of heme transport in the mitochondria.Biochemical Society transactions · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Zachary N WilsonDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT, USA.ORCID 0000-0003-4269-4058
Matt WestDepartment of Molecular, Cellular, and Developmental Biology, University of Colorado Boulder, Boulder, CO, USA.ORCID 0000-0002-4710-9252
Alyssa M EnglishDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT, USA.ORCID 0000-0001-6031-8748
Greg OdorizziDepartment of Molecular, Cellular, and Developmental Biology, University of Colorado Boulder, Boulder, CO, USA.ORCID 0000-0002-1143-1098
Adam L HughesDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT, USA.ORCID 0000-0002-7095-3793

Funding

TRAINING IN CARDIOVASCULAR RESEARCHT32HL007576 · NHLBI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Stavros George Drakos, Robin M Shaw · 1985 to 2026
$10.6M
TRAINING PROGRAM IN GENETICST32GM007464 · NIGMS · UNIVERSITY OF UTAH · PI GRUNWALD, DAVID J., STANFIELD, GILLIAN · 1985 to 2020
$6.1M
Regulation of Mitochondrial HomeostasisR35GM119694 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Adam Hughes · 2016 to 2026
$4.2M
The Role of the Lysosome in AgingR01AG061376 · NIA · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Adam Hughes · 2018 to 2026
$3.3M
Membrane trafficking to lysosomeshttps://apps.era.nih.gov/gmii/manage/view.era?applId=11030651#R35GM149202 · NIGMS · UNIVERSITY OF COLORADO · PI CHARLES G ODORIZZI · 2023 to 2026
$2.2M
American Cancer Society PF-20-018-01-CCGAmerican Heart Association 20POST35200110NHLBI NIH HHS T32 HL007576NIA NIH HHS R01 AG061376NIGMS NIH HHS R35 GM119694NIGMS NIH HHS R35 GM149202NIGMS NIH HHS T32 GM007464NIH HHS T32GM007464Southern MultifoodsUnited Mitochondrial Disease Foundation PF-19-0209
6 · The paper itself

Abstract

Preserving the health of the mitochondrial network is critical to cell viability and longevity. To do so, mitochondria employ several membrane remodeling mechanisms, including the formation of mitochondrial-derived vesicles (MDVs) and compartments (MDCs) to selectively remove portions of the organelle. In contrast to well-characterized MDVs, the distinguishing features of MDC formation and composition remain unclear. Here, we used electron tomography to observe that MDCs form as large, multilamellar domains that generate concentric spherical compartments emerging from mitochondrial tubules at ER-mitochondria contact sites. Time-lapse fluorescence microscopy of MDC biogenesis revealed that mitochondrial membrane extensions repeatedly elongate, coalesce, and invaginate to form these compartments that encase multiple layers of membrane. As such, MDCs strongly sequester portions of the outer mitochondrial membrane, securing membrane cargo into a protected domain, while also enclosing cytosolic material within the MDC lumen. Collectively, our results provide a model for MDC formation and describe key features that distinguish MDCs from other previously identified mitochondrial structures and cargo-sorting domains.

Indexed as

CytosolMitochondriaMitochondrial MembranesAnimalsElectron Microscope TomographyEndoplasmic ReticulumHeLa CellsHumans

Identifiers

PMID39136939
PMCPMC11320809

What Socratic holds

Textmetadata
LicenceCC BY-NC-SA
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.