Evidence map›Paper›PMID 34217204›Full record

ArticleBMC genomics2021

Maternal cold exposure induces distinct transcriptome changes in the placenta and fetal brown adipose tissue in mice.

Sujoy Ghosh, Chul-Hong Park, Jisu Lee, Nathan Lee, Rui Zhang, Clara Huesing, Dorien Reijnders, Jennifer Sones, Heike Münzberg, Leanne Redman and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Thermoneutrality effects on developmental programming of obesity.Journal of developmental origins of health and disease · 2023
    Article
  5. Article
  6. 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

11 authors at 2 institutions in 2 countries.

Sujoy Ghosh *Genomics and Bioinformatics Core, Pennington Biomedical Research Center, 6400 Perkins Road, Baton Rouge, USA.
Chul-Hong Park *Gene Regulation and Metabolism, Pennington Biomedical Research Center, 6400 Perkins Road, Baton Rouge, Louisiana, 70808, USA.
Jisu Lee *Gene Regulation and Metabolism, Pennington Biomedical Research Center, 6400 Perkins Road, Baton Rouge, Louisiana, 70808, USA.
Nathan LeeLeptin Signaling in The Brain, Pennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Rui ZhangLeptin Signaling in The Brain, Pennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Clara HuesingLeptin Signaling in The Brain, Pennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Dorien ReijndersLouisiana State University School of Veterinary Medicine, Baton Rouge, Louisiana, USA.
Jennifer SonesLouisiana State University School of Veterinary Medicine, Baton Rouge, Louisiana, USA.
Heike MünzbergLeptin Signaling in The Brain, Pennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Leanne RedmanReproductive Endocrinology and Women's Health, Pennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Ji Suk ChangGene Regulation and Metabolism, Pennington Biomedical Research Center, 6400 Perkins Road, Baton Rouge, Louisiana, 70808, USA. jisuk.chang@pbrc.edu.ORCID http://orcid.org/0000-0002-0706-1960
Pennington Biomedical Research Center · USLouisiana State University · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Leigh Lamonica · 2012 to 2026
$69.1M
Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2005 to 2026
$26.5M
Transgenics CoreP30GM118430 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2016 to 2020
$5.8M
Leptin and Central Control of ThermoregulationR01DK092587 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MUENZBERG-GRUENING, HEIKE · 2012 to 2024
$3.5M
Genetically-based neuro-modulation of adipose tissue functionsOT2OD023864 · OD · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MUENZBERG-GRUENING, HEIKE · 2016 to 2019
$3.1M
The short isoform of PGC-1alpha in the control of brown adipose tissue thermogenesisR01DK104748 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI CHANG, JI SUK · 2015 to 2019
$1.7M
American Heart Association-American Stroke Association 10SDG4230068Ministry of Health Singapore WBS R913200076263NIDDK NIH HHS 2 R01 DK092587-06A1NIDDK NIH HHS P30 DK072476NIDDK NIH HHS P30-DK072476NIDDK NIH HHS R01 DK092587NIDDK NIH HHS R01 DK104748NIDDK NIH HHS R01DK104748NIGMS NIH HHS 1P30GM118430-01NIGMS NIH HHS 2-U54-GM-104940NIGMS NIH HHS P30 GM118430NIGMS NIH HHS U54 GM104940NIH HHS 1 OT2 OD23864-01NIH HHS OT2 OD023864
6 · The paper itself

Abstract

backgroundBrown adipose tissue (BAT) is specialized to dissipate energy in the form of heat. BAT-mediated heat production in rodents and humans is critical for effective temperature adaptation of newborns to the extrauterine environment immediately after birth. However, very little is known about whether and how fetal BAT development is modulated in-utero in response to changes in maternal thermal environment during pregnancy. Using BL6 mice, we evaluated the impact of different maternal environmental temperatures (28 °C and 18 °C) on the transcriptome of the placenta and fetal BAT to test if maternal cold exposure influences fetal BAT development via placental remodeling.

resultsMaternal weight gain during pregnancy, the average number of fetuses per pregnancy, and placental weight did not differ between the groups at 28 °C and 18 °C. However, the average fetal weight at E18.5 was 6% lower in the 18 °C-group compared to the 28 °C-group. In fetal BATs, cold exposure during pregnancy induced increased expression of genes involved in de novo lipogenesis and lipid metabolism while decreasing the expression of genes associated with muscle cell differentiation, thus suggesting that maternal cold exposure may promote fetal brown adipogenesis by suppressing the myogenic lineage in bidirectional progenitors. In placental tissues, maternal cold exposure was associated with upregulation of genes involved in complement activation and downregulation of genes related to muscle contraction and actin-myosin filament sliding. These changes may coordinate placental adaptation to maternal cold exposure, potentially by protecting against cold stress-induced inflammatory damage and modulating the vascular and extravascular contractile system in the placenta.

conclusionsThese findings provide evidence that environmental cold temperature sensed by the mother can modulate the transcriptome of placental and fetal BAT tissues. The ramifications of the observed gene expression changes warrant future investigation.

Indexed as

Adipose Tissue, BrownCold TemperatureAnimalsFemaleFetusMicePlacentaPregnancyThermogenesisTranscriptomeBrown adipose tissue thermogenesisFetal brown adipogenesisGene expressionMaternal-fetal crosstalkPlacentaRNA-sequencing

Identifiers

PMID34217204
PMCPMC8254942
OpenAlexW3180494194

What OpenQuestion holds

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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 OpenQuestion graph.