Evidence map›Paper›PMID 32141504›Full record

ArticleEndocrinology2020

Essential Role of Syntaxin-Binding Protein-1 in the Regulation of Glucagon-Like Peptide-1 Secretion.

Jhenielle R Campbell, Alexandre Martchenko, Maegan E Sweeney, Michael F Maalouf, Arianna Psichas, Fiona M Gribble, Frank Reimann, Patricia L Brubaker

Open access · hybridAbstract read
In one paragraph

Article in Endocrinology, 2020. 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
5.7field-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

22 citing papers in PubMed, 36 citations in OpenAlex.

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  19. Proglucagon-Derived Peptides as Therapeutics.Frontiers in endocrinology · 2021
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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

8 authors at 2 institutions in 2 countries.

Jhenielle R CampbellDepartments of Physiology, University of Toronto, Toronto, ON, Canada.
Alexandre MartchenkoDepartments of Physiology, University of Toronto, Toronto, ON, Canada.
Maegan E SweeneyDepartments of Physiology, University of Toronto, Toronto, ON, Canada.
Michael F MaaloufDepartments of Physiology, University of Toronto, Toronto, ON, Canada.
Arianna PsichasDepartments of Medicine, University of Toronto, Toronto, ON, Canada.
Fiona M GribbleDepartments of Medicine, University of Toronto, Toronto, ON, Canada.
Frank ReimannDepartments of Medicine, University of Toronto, Toronto, ON, Canada.
Patricia L BrubakerDepartments of Physiology, University of Toronto, Toronto, ON, Canada.
University of Toronto · CAWellcome/MRC Institute of Metabolic Science · GB

Funding

CIHR PJT-14853Medical Research Council MC_UU_00014/3Medical Research Council MC_UU_00014/5Medical Research Council MC_UU_12012/3Medical Research Council MC_UU_12012/5Medical Research Council MRC_MC_UU_12012/3Wellcome TrustWellcome Trust 106262/Z/14/ZWellcome Trust 106263/Z/14/Z
6 · The paper itself

Abstract

Circadian secretion of the incretin, glucagon-like peptide-1 (GLP-1), correlates with expression of the core clock gene, Bmal1, in the intestinal L-cell. Several SNARE proteins known to be circadian in pancreatic α- and β-cells are also necessary for GLP-1 secretion. However, the role of the accessory SNARE, Syntaxin binding protein-1 (Stxbp1; also known as Munc18-1) in the L-cell is unknown. The aim of this study was to determine whether Stxbp1 is under circadian regulation in the L-cell and its role in the control of GLP-1 secretion. Stxbp1 was highly-enriched in L-cells, and STXBP1 was expressed in a subpopulation of L-cells in mouse and human intestinal sections. Stxbp1 transcripts and protein displayed circadian patterns in mGLUTag L-cells line, while chromatin-immunoprecipitation revealed increased interaction between BMAL1 and Stxbp1 at the peak time-point of the circadian pattern. STXBP1 recruitment to the cytosol and plasma membrane within 30 minutes of L-cell stimulation was also observed at this time-point. Loss of Stxbp1 in vitro and in vivo led to reduced stimulated GLP-1 secretion at the peak time-point of circadian release, and impaired GLP-1 secretion ex vivo. In conclusion, Stxbp1 is a circadian regulated exocytotic protein in the intestinal L-cell that is an essential regulatory component of GLP-1 secretion.

Indexed as

AnimalsARNTL Transcription FactorsCell LineCell MembraneCircadian RhythmEnteroendocrine CellsExocytosisGlucagon-Like Peptide 1HumansIleumMice, Inbred C57BLMice, KnockoutMice, TransgenicMunc18 ProteinsProtein BindingARNTL Transcription FactorsGlucagon-Like Peptide 1Munc18 ProteinsenteroendocrineexocytosisGLP-1glucagonMunc18-1SNAREStxbp1

Identifiers

PMID32141504
PMCPMC7124137
OpenAlexW3009202307

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.