Evidence map›Paper›PMID 37685917›Full record

ArticleInternational journal of molecular sciences2023

Molecular Relay Stations in Membrane Nanotubes: IRSp53 Involved in Actin-Based Force Generation.

Tamás Madarász, Brigitta Brunner, Henriett Halász, Elek Telek, János Matkó, Miklós Nyitrai, Edina Szabó-Meleg

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Intercellular Highways in Transport Processes.Results and problems in cell differentiation · 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 at 2 institutions in 1 country.

Tamás MadarászDepartment of Biophysics, Medical School, University of Pécs, H-7624 Pécs, Hungary.
Brigitta BrunnerInstitute of Biology, Faculty of Sciences, University of Pécs, H-7624 Pécs, Hungary.ORCID 0000-0003-4449-8755
Henriett HalászDepartment of Biophysics, Medical School, University of Pécs, H-7624 Pécs, Hungary.
Elek TelekDepartment of Biophysics, Medical School, University of Pécs, H-7624 Pécs, Hungary.ORCID 0000-0003-0396-4799
János MatkóDepartment of Immunology, Faculty of Science, Eötvös Loránd University, H-1117 Budapest, Hungary.
Miklós NyitraiDepartment of Biophysics, Medical School, University of Pécs, H-7624 Pécs, Hungary.
Edina Szabó-MelegDepartment of Biophysics, Medical School, University of Pécs, H-7624 Pécs, Hungary.ORCID 0000-0002-3315-647X
University of Pecs · HUEötvös Loránd University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Membrane nanotubes are cell protrusions that grow to tens of micrometres and functionally connect cells. Actin filaments are semi-flexible polymers, and their polymerisation provides force for the formation and growth of membrane nanotubes. The molecular bases for the provision of appropriate force through such long distances are not yet clear. Actin filament bundles are likely involved in these processes; however, even actin bundles weaken when growing over long distances, and there must be a mechanism for their regeneration along the nanotubes. We investigated the possibility of the formation of periodic molecular relay stations along membrane nanotubes by describing the interactions of actin with full-length IRSp53 protein and its N-terminal I-BAR domain. We concluded that I-BAR is involved in the early phase of the formation of cell projections, while IRSp53 is also important for the elongation of protrusions. Considering that IRSp53 binds to the membrane along the nanotubes and nucleates actin polymerisation, we propose that, in membrane nanotubes, IRSp53 establishes molecular relay stations for actin polymerisation and, as a result, supports the generation of force required for the growth of nanotubes.

Indexed as

ActinsNanotubesActin CytoskeletonAnimalsCell Membrane StructuresChlorocebus aethiopsMiceMicrovilliNerve Tissue ProteinsActinsBaiap2 protein, mouseNerve Tissue Proteinsactinfluorescence microscopyIRSp53membrane nanotubeprotein–protein interactions

Identifiers

PMID37685917
PMCPMC10487789
OpenAlexW4386098275

What OpenQuestion holds

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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.