Evidence map›Paper›PMID 33184223›Full record

ArticleGenes & development2020

The core clock transcription factor BMAL1 drives circadian β-cell proliferation during compensatory regeneration of the endocrine pancreas.

Volodymyr Petrenko, Miri Stolovich-Rain, Bart Vandereycken, Laurianne Giovannoni, Kai-Florian Storch, Yuval Dor, Simona Chera, Charna Dibner

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 4 countries.

Volodymyr PetrenkoDivision of Endocrinology, Diabetes, Nutrition, and Patient Education, Department of Medicine, University of Geneva, 1211 Geneva, Switzerland.
Miri Stolovich-RainDepartment of Developmental Biology and Cancer Research, The Institute for Medical Research Israel-Canada, The Hebrew University-Hadassah Medical School, Jerusalem 91120, Israel.
Bart VandereyckenSection of Mathematics, University of Geneva, 1211 Geneva, Switzerland.
Laurianne GiovannoniDivision of Endocrinology, Diabetes, Nutrition, and Patient Education, Department of Medicine, University of Geneva, 1211 Geneva, Switzerland.
Kai-Florian StorchDepartment of Psychiatry, McGill University, Montreal, Quebec H4H 1R3, Canada.
Yuval DorDepartment of Developmental Biology and Cancer Research, The Institute for Medical Research Israel-Canada, The Hebrew University-Hadassah Medical School, Jerusalem 91120, Israel.
Simona CheraDepartment of Clinical Science, University of Bergen, 5021 Bergen, Norway.
Charna DibnerDivision of Endocrinology, Diabetes, Nutrition, and Patient Education, Department of Medicine, University of Geneva, 1211 Geneva, Switzerland.
University of Geneva · CHHebrew University of Jerusalem · ILMcGill University · CAUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circadian clocks in pancreatic islets participate in the regulation of glucose homeostasis. Here we examined the role of these timekeepers in β-cell regeneration after the massive ablation of β cells by doxycycline-induced expression of diphtheria toxin A (DTA) in Insulin-rtTA/TET-DTA mice. Since we crossed reporter genes expressing α- and β-cell-specific fluorescent proteins into these mice, we could follow the fate of α- and β cells separately. As expected, DTA induction resulted in an acute hyperglycemia, which was accompanied by dramatic changes in gene expression in residual β cells. In contrast, only temporal alterations of gene expression were observed in α cells. Interestingly, β cells entered S phase preferentially during the nocturnal activity phase, indicating that the diurnal rhythm also plays a role in the orchestration of β-cell regeneration. Indeed, in arrhythmic

Indexed as

AnimalsARNTL Transcription FactorsCell ProliferationCircadian RhythmGlucagon-Secreting CellsInsulin-Secreting CellsMicePancreasRegenerationTranscriptomeARNTL Transcription FactorsBmal1 protein, mousecircadian clockworkdiabetesglucose metabolismInsulin-rtTA/TET-DTA mouse modelpancreatic α and β cellsβ-cell proliferationβ-cell regeneration

Identifiers

PMID33184223
PMCPMC7706703
OpenAlexW3100728558

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.