Evidence map›Paper›PMID 34769479›Full record

ArticleInternational journal of molecular sciences2021

Tks5 Regulates Synaptic Podosome Formation and Stabilization of the Postsynaptic Machinery at the Neuromuscular Junction.

Marcin Pęziński, Kamila Maliszewska-Olejniczak, Patrycja Daszczuk, Paula Mazurek, Paweł Niewiadomski, Maria Jolanta Rędowicz

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. 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 37% 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, 8 citations in OpenAlex.

  1. Potential therapeutic targeting of BKMolecular oncology · 2026
    Review
  2. Article
  3. Understanding Actin Remodeling in Neuronal Cells Through Podosomes.Methods in molecular biology (Clifton, N.J.) · 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

6 authors at 1 institution in 1 country.

Marcin PęzińskiLaboratory of Synaptogenesis, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-787 Warszawa, Poland.
Kamila Maliszewska-OlejniczakLaboratory of Synaptogenesis, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-787 Warszawa, Poland.
Patrycja DaszczukLaboratory of Synaptogenesis, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-787 Warszawa, Poland.
Paula MazurekLaboratory of Synaptogenesis, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-787 Warszawa, Poland.
Paweł NiewiadomskiLaboratory of Synaptogenesis, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-787 Warszawa, Poland.ORCID 0000-0001-6254-6162
Maria Jolanta RędowiczLaboratory of Molecular Basis of Cell Motility, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-787 Warszawa, Poland.ORCID 0000-0001-5834-471X
Instytut Biologii Doświadczalnej im. Marcelego Nenckiego · PL

Funding

National Science Center UMO-2014/13/B/NZ3/00909National Science Center UMO-2018/29/N/NZ4/02724
6 · The paper itself

Abstract

Currently, the etiology of many neuromuscular disorders remains unknown. Many of them are characterized by aberrations in the maturation of the neuromuscular junction (NMJ) postsynaptic machinery. Unfortunately, the molecular factors involved in this process are still largely unknown, which poses a great challenge for identifying potential therapeutic targets. Here, we identified Tks5 as a novel interactor of αdystrobrevin-1, which is a crucial component of the NMJ postsynaptic machinery. Tks5 has been previously shown in cancer cells to be an important regulator of actin-rich structures known as invadosomes. However, a role of this scaffold protein at a synapse has never been studied. We show that Tks5 is crucial for remodeling of the NMJ postsynaptic machinery by regulating the organization of structures similar to the invadosomes, known as synaptic podosomes. Additionally, it is involved in the maintenance of the integrity of acetylcholine receptor (AChR) clusters and regulation of their turnover. Lastly, our data indicate that these Tks5 functions may be mediated by its involvement in recruitment of actin filaments to the postsynaptic machinery. Collectively, we show for the first time that the Tks5 protein is involved in regulation of the postsynaptic machinery.

Indexed as

AnimalsCells, CulturedHEK293 CellsHumansMaleMiceMice, Inbred C57BLNeuromuscular JunctionPhosphate-Binding ProteinsPodosomesPost-Synaptic DensityRNA, Small InterferingSynapsesFish protein, mousePhosphate-Binding ProteinsRNA, Small Interferingactinneuromuscular junctionpodosomespostsynaptic machineryrapsynTks5

Identifiers

PMID34769479
PMCPMC8585010
OpenAlexW3214191101

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.