Evidence map›Paper›PMID 24737317›Full record

ArticleThe Journal of biological chemistry2014

Syntaxin13 expression is regulated by mammalian target of rapamycin (mTOR) in injured neurons to promote axon regeneration.

Yongcheol Cho, Valentina Di Liberto, Dan Carlin, Namiko Abe, Kathy H Li, Alma L Burlingame, Shenheng Guan, Izhak Michaelevski, Valeria Cavalli

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 26% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

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  9. VAMP3 and SNAP23 mediate the disturbed flow-induced endothelial microRNA secretion and smooth muscle hyperplasia.Proceedings of the National Academy of Sciences of the United States of America · 2017
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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

9 authors at 1 institution in 1 country.

Yongcheol ChoFrom the Department of Anatomy and Neurobiology, Washington University in St Louis, School of Medicine, St. Louis, Missouri 63110.
Valentina Di LibertoFrom the Department of Anatomy and Neurobiology, Washington University in St Louis, School of Medicine, St. Louis, Missouri 63110.
Dan CarlinFrom the Department of Anatomy and Neurobiology, Washington University in St Louis, School of Medicine, St. Louis, Missouri 63110.
Namiko AbeFrom the Department of Anatomy and Neurobiology, Washington University in St Louis, School of Medicine, St. Louis, Missouri 63110.
Kathy H Lithe Mass Spectrometry Facility, Department of Pharmaceutical Chemistry, University of California at San Francisco, San Francisco, California 94158-2517, and.
Alma L Burlingamethe Mass Spectrometry Facility, Department of Pharmaceutical Chemistry, University of California at San Francisco, San Francisco, California 94158-2517, and.
Shenheng Guanthe Mass Spectrometry Facility, Department of Pharmaceutical Chemistry, University of California at San Francisco, San Francisco, California 94158-2517, and.
Izhak Michaelevskithe Department of Biochemistry and Molecular Biology, Tel Aviv University, Tel Aviv 69978, Israel.
Valeria CavalliFrom the Department of Anatomy and Neurobiology, Washington University in St Louis, School of Medicine, St. Louis, Missouri 63110, cavalli@pcg.wustl.edu.
Tel Aviv University · IL

Funding

Bio-Organic Biomedical Mass Spectromy ResourceP41GM103481 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BURLINGAME, ALMA L · 2012 to 2015
$6.4M
TSC2 AND ERK SIGNALING IN MTOR-DEPENDENT REGENERATION AND NEUROPATHIC PAINR01DE022000 · NIDCR · WASHINGTON UNIVERSITY · PI CAVALLI, VALERIA · 2011 to 2015
$2.8M
MICROTUBULE POST-TRANSLATIONAL MODIFICATIONS IN AXON REGENERATIONR01NS082446 · NINDS · WASHINGTON UNIVERSITY · PI CAVALLI, VALERIA · 2013 to 2017
$1.7M
NIDCR NIH HHS DE022000NIDCR NIH HHS R01 DE022000NIGMS NIH HHS 8P41GM103481NIGMS NIH HHS P41 GM103481NINDS NIH HHS NS082446NINDS NIH HHS R01 NS082446
6 · The paper itself

Abstract

Injured peripheral neurons successfully activate intrinsic signaling pathways to enable axon regeneration. We have previously shown that dorsal root ganglia (DRG) neurons activate the mammalian target of rapamycin (mTOR) pathway following injury and that this activity enhances their axon growth capacity. mTOR plays a critical role in protein synthesis, but the mTOR-dependent proteins enhancing the regenerative capacity of DRG neurons remain unknown. To identify proteins whose expression is regulated by injury in an mTOR-dependent manner, we analyzed the protein composition of DRGs from mice in which we genetically activated mTOR and from mice with or without a prior nerve injury. Quantitative label-free mass spectrometry analyses revealed that the injury effects were correlated with mTOR activation. We identified a member of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) family of proteins, syntaxin13, whose expression was increased by injury in an mTOR-dependent manner. Increased syntaxin13 levels in injured nerves resulted from local protein synthesis and not axonal transport. Finally, knockdown of syntaxin13 in cultured DRG neurons prevented axon growth and regeneration. Together, these data suggest that syntaxin13 translation is regulated by mTOR in injured neurons to promote axon regeneration.

Indexed as

AnimalsAxonsAxotomyCells, CulturedFemaleGanglia, SpinalMiceMice, Inbred C57BLMice, KnockoutNerve RegenerationProteomicsQa-SNARE ProteinsSciatic NerveSensory Receptor CellsTOR Serine-Threonine KinasesmTOR protein, mouseQa-SNARE Proteinssyntaxin 12, mouseTOR Serine-Threonine KinasesAxonmTORProteomicsRegenerationSNARE Proteins

Identifiers

PMID24737317
PMCPMC4140936
OpenAlexW1985199742

What OpenQuestion holds

Textmetadata
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.