Evidence map›Paper›PMID 36181414›Full record

ArticleJournal of diabetes investigation2023

SNARE-binding protein synaptosomal-associated protein of 29 kDa (SNAP29) regulates the intracellular sequestration of glucose transporter 4 (GLUT4) vesicles in adipocytes.

Kumiko Matsui, Masahiro Emoto, Naofumi Fukuda, Ryuta Nomiyama, Kyoko Yamada, Yukio Tanizawa

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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.

Kumiko MatsuiDepartment of Endocrinology, Metabolism, Hematological Sciences and Therapeutics, Yamaguchi University Graduate School of Medicine, Ube, Japan.ORCID https://orcid.org/0000-0002-2405-5263
Masahiro EmotoDepartment of Endocrinology, Metabolism, Hematological Sciences and Therapeutics, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Naofumi FukudaDepartment of Endocrinology, Metabolism, Hematological Sciences and Therapeutics, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Ryuta NomiyamaDepartment of Endocrinology, Metabolism, Hematological Sciences and Therapeutics, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Kyoko YamadaDepartment of Endocrinology, Metabolism, Hematological Sciences and Therapeutics, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Yukio TanizawaDepartment of Endocrinology, Metabolism, Hematological Sciences and Therapeutics, Yamaguchi University Graduate School of Medicine, Ube, Japan.ORCID https://orcid.org/0000-0002-4742-8245
Yamaguchi University · JP

Funding

Grant-in-Aid for scientific research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan 18659269Grant-in-Aid for scientific research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan 19H03710Grant-in-Aid for scientific research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan 20591060Grant-in-Aid for scientific research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan 24659446Takeda Science Foundation
6 · The paper itself

Abstract

AIMS/

introductionInsulin stimulates translocation of glucose transporter 4 (GLUT4) from the perinuclear location to the plasma membrane. In the unstimulated state, intracellular vesicles containing GLUT4 are sequestered into specialized storage vesicles that have come to be known as the insulin-responsive compartment (IRC). The IRC is a functional compartment in the perinuclear region that is a target of the insulin signaling cascade, although its precise nature is unclear. Here, we report a novel molecular mechanism facilitating formation of the IRC. MATERIALS AND

methodsWe determined synaptosomal-associated protein of 29 kDa (SNAP29) by mass spectrometry to be an EH domain-containing protein 1 (EHD1)-binding protein. Then, its expression was confirmed by western blotting. Subcellular localization of SNAP29 was determined by immunofluorescent microscopy. Interactions between SNAP29 and syntaxins were determined by immunoprecipitation. We measured glucose uptake and GLUT4 translocation in 3T3-L1 adipocyte expressing SNAP29 or silencing SNAP29.

resultsWe found SNAP29 to be localized in the perinuclear region and to show partial co-localization with GLUT4 under basal conditions. We also found that SNAP29 binds to syntaxin6, a Qc-SNARE, in adipocytes. In SNAP29-expressing cells, vesicles containing GLUT4 were observed to aggregate around the perinuclear region. In contrast, when SNAP29 was silenced, perinuclear GLUT4 vesicles were dispersed throughout the cytosol. Insulin-stimulated glucose uptake was inhibited in both SNAP29-expressing and SNAP29-silenced cells.

conclusionsThese data suggest that SNAP29 sequesters and anchors GLUT4-containing vesicles in the perinuclear region, and might have a role in the biogenesis of the perinuclear IRC.

Indexed as

Monosaccharide Transport ProteinsSNARE ProteinsAdipocytesGlucoseGlucose Transporter Type 4Glucose Transport Proteins, FacilitativeHumansInsulinProtein TransportQb-SNARE ProteinsQc-SNARE ProteinsVesicular Transport ProteinsEHD1 protein, humanGlucoseGlucose Transporter Type 4Glucose Transport Proteins, FacilitativeInsulinMonosaccharide Transport ProteinsQb-SNARE ProteinsQc-SNARE ProteinsSNAP29 protein, humanSNARE ProteinsVesicular Transport ProteinsGlucose transporter type 4 (GLUT4)InsulinSynaptosomal-associated protein of 29 kDa (SNAP29)

Identifiers

PMID36181414
PMCPMC9807150
OpenAlexW4298327032

What OpenQuestion holds

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LicenceCC BY-NC
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.