Evidence map›Paper›PMID 25816302›Full record

ArticlePloS one2015

Prolactin receptors and placental lactogen drive male mouse pancreatic islets to pregnancy-related mRNA changes.

Lotte Goyvaerts, Katleen Lemaire, Ingrid Arijs, Julien Auffret, Mikaela Granvik, Leentje Van Lommel, Nadine Binart, Peter in't Veld, Frans Schuit, Anica Schraenen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

  1. Serotonin Influences Insulin Secretion in Rat Insulinoma INS-1E Cells.International journal of molecular sciences · 2024
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Pancreatic β-cell heterogeneity in health and diabetes: classes, sources, and subtypes.American journal of physiology. Endocrinology and metabolism · 2021
    Review
  7. Islet Regeneration: Endogenous and Exogenous Approaches.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Is a β cell a β cell?Current opinion in endocrinology, diabetes, and obesity · 2017
    Review
  15. Article
  16. Article
  17. β-Cell adaptation in pregnancy.Diabetes, obesity & metabolism · 2016
    Review
  18. Review
  19. Article
  20. The prolactin receptor: Diverse and emerging roles in pathophysiology.Journal of clinical & translational endocrinology · 2015
    Review
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

10 authors at 3 institutions in 2 countries.

Lotte GoyvaertsGene Expression Unit, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
Katleen LemaireGene Expression Unit, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
Ingrid ArijsGene Expression Unit, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium; Department of Clinical and Experimental Medicine, Translational Research Center for Gastrointestinal Disorders (TARGID), University Hospital Gasthuisberg, KU Leuven, Leuven, Belgium.
Julien AuffretInserm U693, Faculté de Médecine Paris-Sud, Université Paris-Sud, Le Kremlin-Bicêtre, France.
Mikaela GranvikGene Expression Unit, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
Leentje Van LommelGene Expression Unit, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
Nadine BinartInserm U693, Faculté de Médecine Paris-Sud, Université Paris-Sud, Le Kremlin-Bicêtre, France.
Peter in't VeldDepartment of Pathology, Vrije Universiteit Brussel, Jette, Belgium.
Frans SchuitGene Expression Unit, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
Anica SchraenenGene Expression Unit, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
KU Leuven · BEUniversité Paris-Sud · FRVrije Universiteit Brussel · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pregnancy requires a higher functional beta cell mass and this is associated with profound changes in the gene expression profile of pancreatic islets. Taking Tph1 as a sensitive marker for pregnancy-related islet mRNA expression in female mice, we previously identified prolactin receptors and placental lactogen as key signalling molecules. Since beta cells from male mice also express prolactin receptors, the question arose whether male and female islets have the same phenotypic resilience at the mRNA level during pregnancy. We addressed this question in vitro, by stimulating cultured islets with placental lactogen and in vivo, by transplanting male or female islets into female acceptor mice. Additionally, the islet mRNA expression pattern of pregnant prolactin receptor deficient mice was compared with that of their pregnant wild-type littermates. When cultured with placental lactogen, or when transplanted in female recipients that became pregnant (day 12.5), male islets induced the 'islet pregnancy gene signature', which we defined as the 12 highest induced genes in non-transplanted female islets at day 12.5 of pregnancy. In addition, serotonin immunoreactivity and beta cell proliferation was also induced in these male transplanted islets at day 12.5 of pregnancy. In order to further investigate the importance of prolactin receptors in these mRNA changes we used a prolactin receptor deficient mouse model. For the 12 genes of the signature, which are highly induced in control pregnant mice, no significant induction of mRNA transcripts was found at day 9.5 of pregnancy. Together, our results support the key role of placental lactogen as a circulating factor that can trigger the pregnancy mRNA profile in both male and female beta cells.

Indexed as

AnimalsCell ProliferationCells, CulturedFemaleGene Expression ProfilingInsulin-Secreting CellsMaleMicePlacental LactogenPregnancyReceptors, ProlactinRNA, MessengerPlacental LactogenReceptors, ProlactinRNA, Messenger

Identifiers

PMID25816302
PMCPMC4376745
OpenAlexW2074792343

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Registered trials

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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.