Evidence map›Paper›PMID 37736739›Full record

ArticleBiology direct2023

Depletion of LONP2 unmasks differential requirements for peroxisomal function between cell types and in cholesterol metabolism.

Akihiro Yamashita, Olesia Ignatenko, Mai Nguyen, Raphaëlle Lambert, Kathleen Watt, Caroline Daneault, Isabelle Robillard-Frayne, Ivan Topisirovic, Christine Des Rosiers, Heidi M McBride

Open access · goldAbstract read
In one paragraph

Article in Biology direct, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. AAA+ ATPase chaperone p97/VCPNature communications · 2024
    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

10 authors at 5 institutions in 2 countries.

Akihiro YamashitaMontreal Neurological Institute, McGill University, Montréal, QC, Canada.
Olesia IgnatenkoMontreal Neurological Institute, McGill University, Montréal, QC, Canada.
Mai NguyenMontreal Neurological Institute, McGill University, Montréal, QC, Canada.
Raphaëlle LambertInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.
Kathleen WattDepartment of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden.
Caroline DaneaultMontreal Heart Institute, Université de Montréal, Montréal, Canada.
Isabelle Robillard-FrayneMontreal Heart Institute, Université de Montréal, Montréal, Canada.
Ivan TopisirovicLady Davis Institute, McGill University, Montreal, Canada.
Christine Des RosiersMontreal Heart Institute, Université de Montréal, Montréal, Canada.
Heidi M McBrideMontreal Neurological Institute, McGill University, Montréal, QC, Canada. heidi.mcbride@mcgill.ca.
McGill University · CAUniversité de Montréal · CAMontreal Neurological Institute and Hospital · CAInstitute for Research in Immunology and Cancer · CAKarolinska Institutet · SE

Funding

CIHR PJT-162183
6 · The paper itself

Abstract

Peroxisomes play a central role in tuning metabolic and signaling programs in a tissue- and cell-type-specific manner. However, the mechanisms by which the status of peroxisomes is communicated and integrated into cellular signaling pathways are not yet understood. Herein, we report the cellular responses to peroxisomal proteotoxic stress upon silencing the peroxisomal protease/chaperone LONP2. Depletion of LONP2 triggered the accumulation of its substrate TYSND1 protease, while the overall expression of peroxisomal proteins, as well as TYSND1-dependent ACOX1 processing appeared normal, reflecting early stages of peroxisomal proteotoxic stress. Consequently, the alteration of peroxisome size and numbers, and luminal protein import failure was coupled with induction of cell-specific cellular stress responses. Specific to COS-7 cells was a strong activation of the integrated stress response (ISR) and upregulation of ribosomal biogenesis gene expression levels. Common changes between COS-7 and U2OS cell lines included repression of the retinoic acid signaling pathway and upregulation of sphingolipids. Cholesterol accumulated in the endomembrane compartments in both cell lines, consistent with evidence that peroxisomes are required for cholesterol flux out of late endosomes. These unexpected consequences of peroxisomal stress provide an important insight into our understanding of the tissue-specific responses seen in peroxisomal disorders.

Indexed as

EndosomesSignal TransductionPeptide HydrolasesRibosomesUp-RegulationPeptide Hydrolases

Identifiers

PMID37736739
PMCPMC10515011
OpenAlexW4386945539

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.