Evidence map›Paper›PMID 24841562›Full record

ArticleThe Journal of cell biology2014

The late endosomal p14-MP1 (LAMTOR2/3) complex regulates focal adhesion dynamics during cell migration.

Natalia Schiefermeier, Julia M Scheffler, Mariana E G de Araujo, Taras Stasyk, Teodor Yordanov, Hannes L Ebner, Martin Offterdinger, Sebastian Munck, Michael W Hess, Sara A Wickström and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

63 citing papers in PubMed, 101 citations in OpenAlex.

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  13. Hax1 regulate focal adhesion dynamics through IQGAP1.Cell communication and signaling : CCS · 2023
    Article
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  15. Review
  16. Spatial organization of lysosomal exocytosis relies on membrane tension gradients.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
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3 more citing papers are in PubMed but not listed here.

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

15 authors at 5 institutions in 4 countries.

Natalia SchiefermeierDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, AustriaDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, Austria.
Julia M SchefflerDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, Austria.
Mariana E G de AraujoDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, Austria.
Taras StasykDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, Austria.
Teodor YordanovDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, Austria.
Hannes L EbnerDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, AustriaDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, Austria.
Martin OffterdingerDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, Austria.
Sebastian MunckVIB Center for the Biology of Disease, KU Leuven, 3000 Leuven, Belgium.
Michael W HessDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, Austria.
Sara A WickströmPaul Gerson Unna group "Skin Homeostasis and Ageing", Max Planck Institute for Biology of Ageing, 50931 Cologne, Germany Department of Molecular Medicine, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
Anika LangeDepartment of Molecular Medicine, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
Winfried WunderlichDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, Austria Oncotyrol, 6020 Innsbruck, Austria.
Reinhard FässlerDepartment of Molecular Medicine, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
David TeisDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, Austria.
Lukas A HuberDivision of Cell Biology and Division of Neurobiochemistry/Biooptics, Biocenter, Department of Physiology and Medical Physics, Division of Physiology, Department of Traumatology, Center of Operative Medicine, and Division of Histology and Embryology, Innsbruck Medical University, 6020 Innsbruck, Austria lukas.a.huber@i-med.ac.at.
Co-operative College · GBInnsbruck Medical University · ATMax Planck Institute of Biochemistry · DEMax Planck Institute for Biology · DEVIB-KU Leuven Center for Cancer Biology · BE

Funding

Austrian Science Fund FWF W 1101Austrian Science Fund FWF Y 444
6 · The paper itself

Abstract

Cell migration is mediated by the dynamic remodeling of focal adhesions (FAs). Recently, an important role of endosomal signaling in regulation of cell migration was recognized. Here, we show an essential function for late endosomes carrying the p14-MP1 (LAMTOR2/3) complex in FA dynamics. p14-MP1-positive endosomes move to the cell periphery along microtubules (MTs) in a kinesin1- and Arl8b-dependent manner. There they specifically target FAs to regulate FA turnover, which is required for cell migration. Using genetically modified fibroblasts from p14-deficient mice and Arl8b-depleted cells, we demonstrate that MT plus end-directed traffic of p14-MP1-positive endosomes triggered IQGAP1 disassociation from FAs. The release of IQGAP was required for FA dynamics. Taken together, our results suggest that late endosomes contribute to the regulation of cell migration by transporting the p14-MP1 scaffold complex to the vicinity of FAs.

Indexed as

Adaptor Proteins, Signal TransducingADP-Ribosylation FactorsAnimalsCell LineCell MovementEndosomesFibroblastsFocal AdhesionsHeLa CellsHumansMiceMice, 129 StrainMice, Inbred C57BLMice, KnockoutMolecular Sequence DataNIH 3T3 CellsAdaptor Proteins, Signal TransducingADP-Ribosylation FactorsArl8B protein, mouseIQ motif containing GTPase activating protein 1LAMTOR2 protein, mouseLamtor3 protein, mouseProteinsras GTPase-Activating Proteins

Identifiers

PMID24841562
PMCPMC4033770
OpenAlexW2008124485

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.