Evidence map›Paper›PMID 25589673›Full record

ArticleMolecular biology of the cell2015

CLASP2-dependent microtubule capture at the neuromuscular junction membrane requires LL5β and actin for focal delivery of acetylcholine receptor vesicles.

Sreya Basu, Stefan Sladecek, Isabel Martinez de la Peña y Valenzuela, Mohammed Akaaboune, Ihor Smal, Katrin Martin, Niels Galjart, Hans Rudolf Brenner

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Insulin secretion hot spots in pancreatic β cells as secreting adhesions.Frontiers in cell and developmental biology · 2023
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. CLASPs at a glance.Journal of cell science · 2020
    Review
  14. Article
  15. Article
  16. Article
  17. PIPScientific reports · 2019
    Article
  18. Article
  19. Article
  20. 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

8 authors at 3 institutions in 3 countries.

Sreya BasuDepartment of Biomedicine, University of Basel, CH-4056 Basel, Switzerland Department of Cell Biology, Erasmus Medical Center, 3015 GE Rotterdam, Netherlands.
Stefan SladecekDepartment of Biomedicine, University of Basel, CH-4056 Basel, Switzerland.
Isabel Martinez de la Peña y ValenzuelaDepartment of Molecular, Cellular, and Developmental Biology and Program in Neuroscience, University of Michigan, Ann Arbor, MI 48109.
Mohammed AkaabouneDepartment of Molecular, Cellular, and Developmental Biology and Program in Neuroscience, University of Michigan, Ann Arbor, MI 48109.
Ihor SmalBiomedical Imaging Group, Erasmus Medical Center, 3015 GE Rotterdam, Netherlands.
Katrin MartinDepartment of Biomedicine, University of Basel, CH-4056 Basel, Switzerland.
Niels GaljartDepartment of Cell Biology, Erasmus Medical Center, 3015 GE Rotterdam, Netherlands.
Hans Rudolf BrennerDepartment of Biomedicine, University of Basel, CH-4056 Basel, Switzerland Hans-Rudolf.Brenner@unibas.ch n.galjart@erasmusmc.nl.
University of Basel · CHUniversity of Michigan · USErasmus MC · NL

Funding

The Dynamics of Synaptic Component at the Neuromuscular Junction of Living AnimalR01NS047332 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI AKAABOUNE, MOHAMMED · 2003 to 2013
$2.7M
NINDS NIH HHS NS-047332NINDS NIH HHS R01 NS047332
6 · The paper itself

Abstract

A hallmark of the neuromuscular junction (NMJ) is the high density of acetylcholine receptors (AChRs) in the postsynaptic muscle membrane. The postsynaptic apparatus of the NMJ is organized by agrin secreted from motor neurons. The mechanisms that underlie the focal delivery of AChRs to the adult NMJ are not yet understood in detail. We previously showed that microtubule (MT) capture by the plus end-tracking protein CLASP2 regulates AChR density at agrin-induced AChR clusters in cultured myotubes via PI3 kinase acting through GSK3β. Here we show that knockdown of the CLASP2-interaction partner LL5β by RNAi and forced expression of a CLASP2 fragment blocking the CLASP2/LL5β interaction inhibit microtubule capture. The same treatments impair focal vesicle delivery to the clusters. Consistent with these findings, knockdown of LL5β at the NMJ in vivo reduces the density and insertion of AChRs into the postsynaptic membrane. MT capture and focal vesicle delivery to agrin-induced AChR clusters are also inhibited by microtubule- and actin-depolymerizing drugs, invoking both cytoskeletal systems in MT capture and in the fusion of AChR vesicles with the cluster membrane. Combined our data identify a transport system, organized by agrin through PI3 kinase, GSK3β, CLASP2, and LL5β, for precise delivery of AChR vesicles from the subsynaptic nuclei to the overlying synaptic membrane.

Indexed as

ActinsAgrinAnimalsGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaMembrane ProteinsMiceMicrofilament ProteinsMicrotubule-Associated ProteinsNeuromuscular JunctionPhosphatidylinositol 3-KinasesReceptors, CholinergicSynaptic MembranesTransport VesiclesActinsAgrinCLASP2 protein, mouseGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGsk3b protein, mouseMembrane ProteinsMicrofilament ProteinsMicrotubule-Associated ProteinsPhldb2 protein, mousePhosphatidylinositol 3-KinasesReceptors, Cholinergic

Identifiers

PMID25589673
PMCPMC4342029
OpenAlexW2313399747

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.