Evidence map›Paper›PMID 31784514›Full record

ArticleNature communications2019

SIPA1L2 controls trafficking and local signaling of TrkB-containing amphisomes at presynaptic terminals.

Maria Andres-Alonso, Mohamed Raafet Ammar, Ioana Butnaru, Guilherme M Gomes, Gustavo Acuña Sanhueza, Rajeev Raman, PingAn Yuanxiang, Maximilian Borgmeyer, Jeffrey Lopez-Rojas, Syed Ahsan Raza and 13 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

53 citing papers in PubMed, 91 citations in OpenAlex.

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  12. Autophagy initiation triggers p150Cellular and molecular life sciences : CMLS · 2024
    Article
  13. Testing SIPA1L2 as a modifier of CMT1A using mouse models.Journal of neuropathology and experimental neurology · 2024
    Article
  14. Review
  15. Article
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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

23 authors at 4 institutions in 1 country.

Maria Andres-AlonsoLeibniz Group 'Dendritic Organelles and Synaptic Function', Center for Molecular Neurobiology, ZMNH, University Medical Center Hamburg-Eppendorf, 20251, Hamburg, Germany.
Mohamed Raafet AmmarRG Neuroplasticity, Leibniz Institute for Neurobiology, 39118, Magdeburg, Germany.
Ioana ButnaruRG Neuroplasticity, Leibniz Institute for Neurobiology, 39118, Magdeburg, Germany.
Guilherme M GomesRG Neuroplasticity, Leibniz Institute for Neurobiology, 39118, Magdeburg, Germany.ORCID http://orcid.org/0000-0001-8566-4284
Gustavo Acuña SanhuezaRG Neuroplasticity, Leibniz Institute for Neurobiology, 39118, Magdeburg, Germany.
Rajeev RamanRG Neuroplasticity, Leibniz Institute for Neurobiology, 39118, Magdeburg, Germany.
PingAn YuanxiangRG Neuroplasticity, Leibniz Institute for Neurobiology, 39118, Magdeburg, Germany.
Maximilian BorgmeyerLeibniz Group 'Dendritic Organelles and Synaptic Function', Center for Molecular Neurobiology, ZMNH, University Medical Center Hamburg-Eppendorf, 20251, Hamburg, Germany.
Jeffrey Lopez-RojasRG Neuroplasticity, Leibniz Institute for Neurobiology, 39118, Magdeburg, Germany.
Syed Ahsan RazaDepartment of Genetics & Molecular Neurobiology, Institute of Biology, Otto-von-Guericke University, 39120, Magdeburg, Germany.
Nicola BriceParadigm Therapeutics Ltd. Cambridge, UK Cerevance, Cambridge, UK.
Torben J HausratInstitute of Molecular Neurogenetics, Center for Molecular Neurobiology, ZMNH, University Medical Center Hamburg-Eppendorf, 20251, Hamburg, Germany.
Tamar MacharadzeRG Neuroplasticity, Leibniz Institute for Neurobiology, 39118, Magdeburg, Germany.
Silvia Diaz-GonzalezLeibniz Group 'Dendritic Organelles and Synaptic Function', Center for Molecular Neurobiology, ZMNH, University Medical Center Hamburg-Eppendorf, 20251, Hamburg, Germany.
Mark CarltonParadigm Therapeutics Ltd. Cambridge, UK Cerevance, Cambridge, UK.
Antonio Virgilio FaillaUKE Microscopy Imaging Facility, University Medical Center Hamburg-Eppendorf, 20246, Hamburg, Germany.
Oliver StorkDepartment of Genetics & Molecular Neurobiology, Institute of Biology, Otto-von-Guericke University, 39120, Magdeburg, Germany.
Michaela SchweizerZMNH Core Facility Morphology and Electron Microscopy, Center for Molecular Neurobiology, ZMNH, University Medical Center Hamburg-Eppendorf, 20251, Hamburg, Germany.
Eckart D GundelfingerCenter for Behavioral Brain Sciences, Otto von Guericke University, 39120, Magdeburg, Germany.ORCID http://orcid.org/0000-0001-9377-7414
Matthias KneusselInstitute of Molecular Neurogenetics, Center for Molecular Neurobiology, ZMNH, University Medical Center Hamburg-Eppendorf, 20251, Hamburg, Germany.
Christina SpilkerRG Neuroplasticity, Leibniz Institute for Neurobiology, 39118, Magdeburg, Germany.ORCID http://orcid.org/0000-0002-7996-7673
Anna KarpovaRG Neuroplasticity, Leibniz Institute for Neurobiology, 39118, Magdeburg, Germany. akarpova@lin-magdeburg.de.
Michael R KreutzLeibniz Group 'Dendritic Organelles and Synaptic Function', Center for Molecular Neurobiology, ZMNH, University Medical Center Hamburg-Eppendorf, 20251, Hamburg, Germany. michael.kreutz@lin-magdeburg.de.
Leibniz Institute for Neurobiology · DEUniversität Hamburg · DECenter for Behavioral Brain Sciences · DEOtto-von-Guericke-Universität Magdeburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amphisomes are organelles of the autophagy pathway that result from the fusion of autophagosomes with late endosomes. While biogenesis of autophagosomes and late endosomes occurs continuously at axon terminals, non-degradative roles of autophagy at boutons are barely described. Here, we show that in neurons BDNF/TrkB traffick in amphisomes that signal locally at presynaptic boutons during retrograde transport to the soma. This is orchestrated by the Rap GTPase-activating (RapGAP) protein SIPA1L2, which connects TrkB amphisomes to a dynein motor. The autophagosomal protein LC3 regulates RapGAP activity of SIPA1L2 and controls retrograde trafficking and local signaling of TrkB. Following induction of presynaptic plasticity, amphisomes dissociate from dynein at boutons enabling local signaling and promoting transmitter release. Accordingly, sipa1l2 knockout mice show impaired BDNF-dependent presynaptic plasticity. Taken together, the data suggest that in hippocampal neurons, TrkB-signaling endosomes are in fact amphisomes that during retrograde transport have local signaling capacity in the context of presynaptic plasticity.

Indexed as

AnimalsAutophagosomesAxonal TransportAxonsBrain-Derived Neurotrophic FactorDyneinsEndosomesGTPase-Activating ProteinsHippocampusMembrane GlycoproteinsMiceMice, KnockoutMicrotubule-Associated ProteinsNeuronal PlasticityNeuronsPresynaptic TerminalsBdnf protein, mouseBrain-Derived Neurotrophic FactorDyneinsGTPase-Activating ProteinsMap1lc3b protein, mouseMembrane GlycoproteinsMicrotubule-Associated ProteinsNtrk2 protein, mouseProtein-Tyrosine KinasesReceptor, trkBsipa1l2 protein, mouse

Identifiers

PMID31784514
PMCPMC6884526
OpenAlexW2991403126

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.