Evidence map›Paper›PMID 36899442›Full record

ArticleCell & bioscience2023

ISL1 controls pancreatic alpha cell fate and beta cell maturation.

Romana Bohuslavova, Valeria Fabriciova, Laura Lebrón-Mora, Jessica Malfatti, Ondrej Smolik, Lukas Valihrach, Sarka Benesova, Daniel Zucha, Zuzana Berkova, Frantisek Saudek and 2 more

Abstract read
In one paragraph

Article in Cell & bioscience, 2023. 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
–field-weighted citation impact
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.

  1. Article
  2. Predictive control of human pancreatic cell fate using a digital model ofbioRxiv : the preprint server for biology · 2026
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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

12 authors.

Romana BohuslavovaLaboratory of Molecular Pathogenetics, Institute of Biotechnology CAS, 25250, Vestec, Czechia. romana.bohuslavova@ibt.cas.cz.
Valeria FabriciovaLaboratory of Molecular Pathogenetics, Institute of Biotechnology CAS, 25250, Vestec, Czechia.
Laura Lebrón-MoraLaboratory of Molecular Pathogenetics, Institute of Biotechnology CAS, 25250, Vestec, Czechia.
Jessica MalfattiLaboratory of Molecular Pathogenetics, Institute of Biotechnology CAS, 25250, Vestec, Czechia.
Ondrej SmolikLaboratory of Molecular Pathogenetics, Institute of Biotechnology CAS, 25250, Vestec, Czechia.
Lukas ValihrachLaboratory of Gene Expression, Institute of Biotechnology CAS, 25250, Vestec, Czechia.
Sarka BenesovaLaboratory of Gene Expression, Institute of Biotechnology CAS, 25250, Vestec, Czechia.
Daniel ZuchaLaboratory of Gene Expression, Institute of Biotechnology CAS, 25250, Vestec, Czechia.
Zuzana BerkovaLaboratory of Pancreatic Islets, Institute for Clinical and Experimental Medicine, 14021, Prague, Czechia.
Frantisek SaudekLaboratory of Pancreatic Islets, Institute for Clinical and Experimental Medicine, 14021, Prague, Czechia.
Sylvia M EvansDepartment of Pharmacology; Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California at San Diego, La Jolla, CA, USA.
Gabriela PavlinkovaLaboratory of Molecular Pathogenetics, Institute of Biotechnology CAS, 25250, Vestec, Czechia. gpavlinkova@ibt.cas.cz.ORCID http://orcid.org/0000-0002-5689-6577

Funding

Akademie Věd České Republiky 86652036Grantová Agentura České Republiky GA19-07378S
6 · The paper itself

Abstract

backgroundGlucose homeostasis is dependent on functional pancreatic α and ß cells. The mechanisms underlying the generation and maturation of these endocrine cells remain unclear.

resultsWe unravel the molecular mode of action of ISL1 in controlling α cell fate and the formation of functional ß cells in the pancreas. By combining transgenic mouse models, transcriptomic and epigenomic profiling, we uncover that elimination of Isl1 results in a diabetic phenotype with a complete loss of α cells, disrupted pancreatic islet architecture, downregulation of key ß-cell regulators and maturation markers of ß cells, and an enrichment in an intermediate endocrine progenitor transcriptomic profile.

conclusionsMechanistically, apart from the altered transcriptome of pancreatic endocrine cells, Isl1 elimination results in altered silencing H3K27me3 histone modifications in the promoter regions of genes that are essential for endocrine cell differentiation. Our results thus show that ISL1 transcriptionally and epigenetically controls α cell fate competence, and ß cell maturation, suggesting that ISL1 is a critical component for generating functional α and ß cells.

Indexed as

Epigenetic histone modificationPancreas developmentPancreatic endocrine cellsTranscriptome

Identifiers

PMID36899442
PMCPMC9999528

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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.