Evidence map›Paper›PMID 38319250›Full record

ArticleThe Journal of cell biology2024

A role for Vps13-mediated lipid transfer at the ER-endosome contact site in ESCRT-mediated sorting.

Sho W Suzuki, Matthew West, Yichen Zhang, Jenny S Fan, Rachel T Roberts, Greg Odorizzi, Scott D Emr

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. Article
  2. Review
  3. Yeast as a Model for Human Disease.International journal of molecular sciences · 2026
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. ESCRTing the RABs through conversion.Biochemical Society transactions · 2025
    Review
  10. Article
  11. Review
  12. Sorting of complex sphingolipids within the cellular endomembrane systems.Frontiers in cell and developmental biology · 2024
    Review
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.

Sho W SuzukiWeill Institute for Cell and Molecular Biology and Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.ORCID 0000-0002-6563-5387
Matthew WestMolecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO, USA.ORCID 0000-0002-4710-9252
Yichen ZhangWeill Institute for Cell and Molecular Biology and Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.ORCID 0009-0006-6834-3992
Jenny S FanWeill Institute for Cell and Molecular Biology and Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.ORCID 0009-0008-8493-2791
Rachel T RobertsWeill Institute for Cell and Molecular Biology and Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.ORCID 0009-0009-5134-0359
Greg OdorizziMolecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO, USA.ORCID 0000-0002-1143-1098
Scott D EmrWeill Institute for Cell and Molecular Biology and Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.ORCID 0000-0002-5408-6781

Funding

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
NIGMS NIH HHS R35 GM149202
6 · The paper itself

Abstract

Endosomes are specialized organelles that function in the secretory and endocytic protein sorting pathways. Endocytosed cell surface receptors and transporters destined for lysosomal degradation are sorted into intraluminal vesicles (ILVs) at endosomes by endosomal sorting complexes required for transport (ESCRT) proteins. The endosomes (multivesicular bodies, MVBs) then fuse with the lysosome. During endosomal maturation, the number of ILVs increases, but the size of endosomes does not decrease despite the consumption of the limiting membrane during ILV formation. Vesicle-mediated trafficking is thought to provide lipids to support MVB biogenesis. However, we have uncovered an unexpected contribution of a large bridge-like lipid transfer protein, Vps13, in this process. Here, we reveal that Vps13-mediated lipid transfer at ER-endosome contact sites is required for the ESCRT pathway. We propose that Vps13 may play a critical role in supplying lipids to the endosome, ensuring continuous ESCRT-mediated sorting during MVB biogenesis.

Indexed as

Endosomal Sorting Complexes Required for TransportEndosomesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsEndocytosisLipidsMultivesicular BodiesProtein TransportEndosomal Sorting Complexes Required for TransportLipidsSaccharomyces cerevisiae ProteinsVPS13 protein, S cerevisiae

Identifiers

PMID38319250
PMCPMC10847051

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.