Evidence map›Paper›PMID 32444826›Full record

ArticleCommunications biology2020

Mitochondrial stress-activated cGAS-STING pathway inhibits thermogenic program and contributes to overnutrition-induced obesity in mice.

Juli Bai, Christopher Cervantes, Sijia He, Jieyu He, George R Plasko, Jie Wen, Zhi Li, Dongqing Yin, Chuntao Zhang, Meilian Liu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
4.0field-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

69 citing papers in PubMed, 97 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. cGAS: bridging immunity and metabolic regulation.Journal of molecular cell biology · 2026
    Review
  6. Article
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  8. Innate immune signalling in the adipocyte.Journal of biochemistry · 2026
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Sterile inflammation in laminopathies.European journal of cell biology · 2025
    Review
  15. Amyloid-beta glycation induces neuronal mitochondrial dysfunction and Alzheimer's pathogenesis via VDAC1-dependent mtDNA efflux.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review

9 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 2 countries.

Juli BaiDepartments of Pharmacology, University of Texas Health San Antonio, San Antonio, TX, USA. BaiJ@uthscsa.edu.
Christopher CervantesDepartments of Pharmacology, University of Texas Health San Antonio, San Antonio, TX, USA.
Sijia HeDepartments of Pharmacology, University of Texas Health San Antonio, San Antonio, TX, USA.
Jieyu HeDepartments of Pharmacology, University of Texas Health San Antonio, San Antonio, TX, USA.
George R PlaskoDepartments of Pharmacology, University of Texas Health San Antonio, San Antonio, TX, USA.
Jie WenDepartments of Pharmacology, University of Texas Health San Antonio, San Antonio, TX, USA.
Zhi LiDepartments of Pharmacology, University of Texas Health San Antonio, San Antonio, TX, USA.
Dongqing YinDepartments of Pharmacology, University of Texas Health San Antonio, San Antonio, TX, USA.
Chuntao ZhangDepartments of Pharmacology, University of Texas Health San Antonio, San Antonio, TX, USA.
Meilian LiuDepartment of Metabolism and Endocrinology and the Metabolic Syndrome Research Center, The Second Xiangya Hospital, Central South University and National Clinical Research center for Metabolic Diseases, Changsha, Hunan, China.ORCID http://orcid.org/0000-0003-1639-262X
Lily Q DongDepartments of Cell Systems & Anatomy, University of Texas Health San Antonio, San Antonio, TX, USA.ORCID http://orcid.org/0000-0002-6293-818X
Feng LiuDepartments of Pharmacology, University of Texas Health San Antonio, San Antonio, TX, USA. Liuf@uthscsa.edu.ORCID http://orcid.org/0000-0002-5098-1711
The University of Texas Health Science Center at San Antonio · USCentral South University · CN

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
Hypothalamic Grb10 and body weightR01DK115761 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI FRAZER, ALAN, XU, YONG · 2018 to 2021
$2.0M
The role of TCTP in regulating adiponectin signalingR01DK102965 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI DONG, LILY Q · 2015 to 2019
$1.7M
Regulation of Mitochondrial Biogenesis and Function by DsbA-L in the LiverR01DK114479 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI FRAZER, ALAN · 2018 to 2021
$1.4M
NCI NIH HHS P30 CA054174NIDDK NIH HHS R01 DK102965NIDDK NIH HHS R01 DK114479NIDDK NIH HHS R01 DK115761NIH HHS DK102965NIH HHS DK114479NIH HHS DK115761
6 · The paper itself

Abstract

Obesity is a global epidemic that is caused by excessive energy intake or inefficient energy expenditure. Brown or beige fat dissipates energy as heat through non-shivering thermogenesis by their high density of mitochondria. However, how the mitochondrial stress-induced signal is coupled to the cellular thermogenic program remains elusive. Here, we show that mitochondrial DNA escape-induced activation of the cGAS-STING pathway negatively regulates thermogenesis in fat-specific DsbA-L knockout mice, a model of adipose tissue mitochondrial stress. Conversely, fat-specific overexpression of DsbA-L or knockout of STING protects mice against high-fat diet-induced obesity. Mechanistically, activation of the cGAS-STING pathway in adipocytes activated phosphodiesterase PDE3B/PDE4, leading to decreased cAMP levels and PKA signaling, thus reduced thermogenesis. Our study demonstrates that mitochondrial stress-activated cGAS-STING pathway functions as a sentinel signal that suppresses thermogenesis in adipose tissue. Targeting adipose cGAS-STING pathway may thus be a potential therapeutic strategy to counteract overnutrition-induced obesity and its associated metabolic diseases.

Indexed as

ThermogenesisAdipocytesAnimalsCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseDiet, High-FatGlutathione TransferaseMaleMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutMitochondriaNucleotidyltransferasesObesityOvernutritionSTING ProteincGAS protein, mouseCyclic Guanosine Monophosphate-Adenosine Monophosphate Synthasedisulfide-bond A oxidoreductase-like protein DsbA-L, mouseGlutathione TransferaseMembrane ProteinsNucleotidyltransferasesSting1 protein, mouseSTING Protein

Identifiers

PMID32444826
PMCPMC7244732
OpenAlexW3028450214

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.