Evidence map›Paper›PMID 19622065›Full record

ArticleBioscience reports2009

Not all mitochondrial carrier proteins support permeability transition pore formation: no involvement of uncoupling protein 1.

Paul G Crichton, Nadeene Parker, Antonio J Vidal-Puig, Martin D Brand

Open access · hybridAbstract read
In one paragraph

Article in Bioscience reports, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. A 20/20 view of ANT function in mitochondrial biology and necrotic cell death.Journal of molecular and cellular cardiology · 2020
    Review
  2. UCP1 deficiency causes brown fat respiratory chain depletion and sensitizes mitochondria to calcium overload-induced dysfunction.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  3. Uncoupling protein 1 controls reactive oxygen species in brown adipose tissue.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. 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

4 authors at 2 institutions in 1 country.

Paul G CrichtonMRC Mitochondrial Biology Unit, Hills Road, Cambridge CB2 0XY, UK. pgc@mrc-mbu.cam.ac.uk
Nadeene Parker
Antonio J Vidal-Puig
Martin D Brand
MRC Mitochondrial Biology Unit · GBAddenbrooke's Hospital · GB

Funding

Medical Research Council G0400192Medical Research Council G0600717Medical Research Council MC_U105663137Wellcome Trust 065326/Z/01/ZWellcome Trust 066750/B/01/Z
6 · The paper itself

Abstract

The mPTP (mitochondrial permeability transition pore) is a non-specific channel that is formed in the mitochondrial inner membrane in response to several stimuli, including elevated levels of matrix calcium. The pore is proposed to be composed of the ANT (adenine nucleotide translocase), voltage-dependent anion channel and cyclophilin D. Knockout studies, however, have demonstrated that ANT is not essential for permeability transition, which has led to the proposal that other members of the mitochondrial carrier protein family may be able to play a similar function to ANT in pore formation. To investigate this possibility, we have studied the permeability transition properties of BAT (brown adipose tissue) mitochondria in which levels of the mitochondrial carrier protein, UCP1 (uncoupling protein 1), can exceed those of ANT. Using an improved spectroscopic assay, we have quantified mPTP formation in de-energized mitochondria from wild-type and Ucp1KO (Ucp1-knockout) mice and assessed the dependence of pore formation on UCP1. When correctly normalized for differences in mitochondrial morphology, we find that calcium-induced mPTP activity is the same in both types of mitochondria, with similar sensitivity to GDP (approximately 50% inhibited), although the portion sensitive to cyclosporin A is higher in mitochondria lacking UCP1 (approximately 80% inhibited, compared with approximately 60% in mitochondria containing UCP1). We conclude that UCP1 is not a component of the cyclosporin A-sensitive mPTP in BAT and that playing a role in mPTP formation is not a general characteristic of the mitochondrial carrier protein family but is, more likely, restricted to specific members including ANT.

Indexed as

Adipose Tissue, BrownAnimalsBlotting, WesternCalciumCyclophilinsCyclosporineDose-Response Relationship, DrugErythritolFemaleIon ChannelsMaleMiceMice, KnockoutMitochondriaMitochondrial ADP, ATP TranslocasesMitochondrial Membrane Transport ProteinsCalciumCyclophilinsCyclosporineErythritolIon ChannelsMitochondrial ADP, ATP TranslocasesMitochondrial Membrane Transport ProteinsMitochondrial Permeability Transition PoreMitochondrial ProteinsPeptidyl-Prolyl Isomerase FPPIF protein, mouseUcp1 protein, mouseUncoupling Protein 1Voltage-Dependent Anion Channels

Identifiers

PMID19622065
PMCPMC2805926
OpenAlexW1984239451

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.