Evidence map›Paper›PMID 28132811›Full record

ArticleCurrent biology : CB2017

The ER-Mitochondria Tethering Complex VAPB-PTPIP51 Regulates Autophagy.

Patricia Gomez-Suaga, Sebastien Paillusson, Radu Stoica, Wendy Noble, Diane P Hanger, Christopher C J Miller

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Current biology : CB, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07705048 (The Role of PTPIP51-VAPB Complex in the Pathogenesis of Periodontal Disease), which is not on this map. Cited by 280 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
280citing papers in PubMed, 1 pooled it
23.5field-weighted citation impact, top 1% 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.

NCT07705048 completednot on this mapstarted 2024, after this paper: background citation

The Role of PTPIP51-VAPB Complex in the Pathogenesis of Periodontal Disease

Typeobservational_patient_registrySponsorInonu UniversityRan2024 to 2024Enrolled60ConditionsPeriodontitis, Gingivitis
3 · Its place in the literature

Who cites it

280 citing papers in PubMed, 1 synthesis or guideline pooled it, 382 citations in OpenAlex.

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220 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Patricia Gomez-SuagaDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RX, UK.
Sebastien PaillussonDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RX, UK.
Radu StoicaDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RX, UK.
Wendy NobleDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RX, UK.
Diane P HangerDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RX, UK.
Christopher C J MillerDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RX, UK. Electronic address: chris.miller@kcl.ac.uk.
King's College London · GB

Funding

Medical Research Council G0501573Parkinson's UK G-1308Wellcome Trust 078662
6 · The paper itself

Abstract

Mitochondria form close physical associations with the endoplasmic reticulum (ER) that regulate a number of physiological functions. One mechanism by which regions of ER are recruited to mitochondria involves binding of the ER protein VAPB to the mitochondrial protein PTPIP51, which act as scaffolds to tether the two organelles. Here, we show that the VAPB-PTPIP51 tethers regulate autophagy. We demonstrate that overexpression of VAPB or PTPIP51 to tighten ER-mitochondria contacts impairs, whereas small interfering RNA (siRNA)-mediated loss of VAPB or PTPIP51 to loosen contacts stimulates, autophagosome formation. Moreover, we show that expression of a synthetic linker protein that artificially tethers ER and mitochondria also reduces autophagosome formation, and that this artificial tether rescues the effects of siRNA loss of VAPB or PTPIP51 on autophagy. Thus, these effects of VAPB and PTPIP51 manipulation on autophagy are a consequence of their ER-mitochondria tethering function. Interestingly, we discovered that tightening of ER-mitochondria contacts by overexpression of VAPB or PTPIP51 impairs rapamycin- and torin 1-induced, but not starvation-induced, autophagy. This suggests that the regulation of autophagy by ER-mitochondria signaling is at least partly dependent upon the nature of the autophagic stimulus. Finally, we demonstrate that the mechanism by which the VAPB-PTPIP51 tethers regulate autophagy involves their role in mediating delivery of Ca

Indexed as

AutophagyBlood ProteinsCalciumEndoplasmic ReticulumGene Expression RegulationHEK293 CellsHumansImmunosuppressive AgentsMitochondriaMitochondrial ProteinsProtein Tyrosine PhosphatasesRNA, Small InterferingSirolimusStarvationVesicular Transport ProteinsBlood ProteinsCalciumImmunosuppressive AgentsMitochondrial ProteinsProtein Tyrosine PhosphatasesRMDN3 protein, humanRNA, Small InterferingSirolimustorinVAPB protein, humanVesicular Transport ProteinsAlzheimer’s diseaseamyotrophic lateral sclerosisautophagycalciumendoplasmic reticulumMAMmitochondriaParkinson’s diseasePTPIP51VAPB

Identifiers

PMID28132811
PMCPMC5300905
OpenAlexW2580573179

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.