Evidence map›Paper›PMID 30395881›Full record

SynthesisBiochimica et biophysica acta. Molecular cell research2019

The protein interaction networks of mucolipins and two-pore channels.

Einar K Krogsaeter, Martin Biel, Christian Wahl-Schott, Christian Grimm

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Biochimica et biophysica acta. Molecular cell research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Review
  3. NAADP-Mediated CaHandbook of experimental pharmacology · 2023
    Article
  4. The intracellular CaProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  5. Two-pore channels: going with the flows.Biochemical Society transactions · 2022
    Article
  6. NAADP-binding proteins find their identity.Trends in biochemical sciences · 2022
    Review
  7. Review
  8. Article
  9. Opioid Modulation of Neuronal Iron and Potential Contributions to NeuroHIV.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. TRP Channels Regulation of Rho GTPases in Brain Context and Diseases.Frontiers in cell and developmental biology · 2020
    Review
  15. NAADP Receptors.Cold Spring Harbor perspectives in biology · 2019
    Review
  16. Endolysosomal CaFrontiers in cell and developmental biology · 2019
    Review
  17. 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 4 institutions in 1 country.

Einar K KrogsaeterDepartment of Pharmacology and Toxicology, Faculty of Medicine, University of Munich (LMU) Nussbaumstrasse 26, 80336 Munich.
Martin BielDepartment of Pharmacy - Center for Drug Research and Center for Integrated Protein Science Munich (CIPSM), Ludwig-Maximilians-Universität München, Germany.
Christian Wahl-SchottHannover Medical School, Institute for Neurophysiology, OE 4230, Carl-Neuberg-Str. 1, 30625 Hannover, Germany.
Christian GrimmDepartment of Pharmacology and Toxicology, Faculty of Medicine, University of Munich (LMU) Nussbaumstrasse 26, 80336 Munich. Electronic address: christian.grimm@cup.uni-muenchen.de.
Center for Integrated Protein Science Munich · DELMU Klinikum · DELudwig-Maximilians-Universität München · DEMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe endolysosomal, non-selective cation channels, two-pore channels (TPCs) and mucolipins (TRPMLs), regulate intracellular membrane dynamics and autophagy. While partially compensatory for each other, isoform-specific intracellular distribution, cell-type expression patterns, and regulatory mechanisms suggest different channel isoforms confer distinct properties to the cell. SCOPE OF REVIEW: Briefly, established TPC/TRPML functions and interaction partners ('interactomes') are discussed. Novel TRPML3 interactors are shown, and a meta-analysis of experimentally obtained channel interactomes conducted. Accordingly, interactomes are compared and contrasted, and subsequently described in detail for TPC1, TPC2, TRPML1, and TRPML3. MAJOR

conclusionsTPC interactomes are well-defined, encompassing intracellular membrane organisation proteins. TRPML interactomes are varied, encompassing cardiac contractility- and chaperone-mediated autophagy proteins, alongside regulators of intercellular signalling. GENERAL SIGNIFICANCE: Comprising recently proposed targets to treat cancers, infections, metabolic disease and neurodegeneration, the advancement of TPC/TRPML understanding is of considerable importance. This review proposes novel directions elucidating TPC/TRPML relevance in health and disease. This article is part of a Special Issue entitled: ECS Meeting edited by Claus Heizmann, Joachim Krebs and Jacques Haiech.

Indexed as

Calcium SignalingAnimalsCalcium ChannelsHumansTransient Receptor Potential ChannelsTwo-Pore ChannelsCalcium ChannelsMCOLN1 protein, humanMCOLN3 protein, humanTPCN1 protein, humanTPCN2 protein, humanTransient Receptor Potential ChannelsTwo-Pore ChannelsTPCTPC1TPC2TRPMLTRPML1TRPML3

Identifiers

PMID30395881
PMCPMC7111325
OpenAlexW2899337597

What OpenQuestion holds

Textmetadata
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.