Evidence map›Paper›PMID 24425864›Full record

ArticleThe Journal of biological chemistry2014

Role of extracellular signal-regulated kinase 5 in adipocyte signaling.

Hong Zhu, Sara Guariglia, Wenjing Li, Deborah Brancho, Zhao V Wang, Philipp E Scherer, Chi-Wing Chow

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Article
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  4. Review
  5. Article
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  12. Premature Physiologic Aging as a Paradigm for Understanding Increased Risk of Adverse Health Across the Lifespan of Survivors of Childhood Cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2018
    Review
  13. Article
  14. Article
  15. Article
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  17. 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

7 authors at 4 institutions in 1 country.

Hong ZhuFrom the Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York 10461.
Sara Guariglia
Wenjing Li
Deborah Brancho
Zhao V Wang
Philipp E Scherer
Chi-Wing Chow
Albert Einstein College of Medicine · USThe University of Texas Southwestern Medical Center · USCollege of Staten Island · USYeshiva University · US

Funding

Novel Mechanisms Regulating the Adipocyte-Brain-Hepatocyte AxisP01DK088761 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI SCHERER, PHILIPP E · 2010 to 2019
$17.4M
Adiponectin, A Protein Secreted From Adipose TissueR01DK055758 · NIDDK · YESHIVA UNIVERSITY · PI SCHERER, PHILIPP E · 2000 to 2024
$10.9M
White Adipose Tissue Physiology, Mitochondrial Function and AdiponectinR01DK099110 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI PHILIPP E SCHERER · 2013 to 2026
$6.7M
Molecular Signaling in AdipocytesR01DK090481 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CHOW, CHI-WING · 2011 to 2014
$1.5M
NIDDK NIH HHS P01 DK088761NIDDK NIH HHS P01-DK088761NIDDK NIH HHS R01 DK055758NIDDK NIH HHS R01 DK090481NIDDK NIH HHS R01-DK0904881NIDDK NIH HHS R01 DK099110NIDDK NIH HHS R01-DK099110NIDDK NIH HHS R01-DK55758
6 · The paper itself

Abstract

Increased adiposity due to energy imbalance is a critical factor of the epidemic crisis of obesity and type II diabetes. In addition to the obvious role in energy storage, regulatory factors are secreted from adipose depots to control appetite and cellular homeostasis. Complex signaling cross-talks within adipocyte are also evident due to the metabolic and immune nature of adipose depots. Here, we uncover a role of extracellular signal-regulated kinase 5 (ERK5) in adipocyte signaling. We find that deletion of ERK5 in adipose depots (adipo-ERK5(-/-)) increases adiposity, in part, due to increased food intake. Dysregulated secretion of adipokines, leptin resistance, and impaired glucose handling are also found in adipo-ERK5(-/-) mice. Mechanistically, we show that ERK5 impinges on transcription factor NFATc4. Decreased phosphorylation at the conserved gate-keeping Ser residues and increased nuclear localization of NFATc4 are found in adipo-ERK5(-/-) mice. We also find attenuated PKA activation in adipo-ERK5(-/-) mice. In response to stimulation of β-adrenergic G-protein-coupled receptor, we find decreased NFATc4 phosphorylation and impaired PKA activation in adipo-ERK5(-/-) mice. Reduced cAMP accumulation and increased phosphodiesterase activity are also found. Together, these results demonstrate integration of ERK5 with NFATc4 nucleo-cytoplasmic shuttling and PKA activation in adipocyte signaling.

Indexed as

AdipocytesAdipokinesAdiposityAnimalsCells, CulturedCyclic AMPCyclic AMP-Dependent Protein KinasesMAP Kinase Signaling SystemMiceMice, KnockoutMitogen-Activated Protein Kinase 7NFATC Transcription FactorsPhosphorylationReceptors, Adrenergic, betaAdipokinesCyclic AMPCyclic AMP-Dependent Protein KinasesMitogen-Activated Protein Kinase 7Nfatc4 protein, mouseNFATC Transcription FactorsReceptors, Adrenergic, betaAdipose tissueMAP Kinases (MAPKs)Metabolic RegulationNFAT Transcription FactorProtein Kinase A (PKA)

Identifiers

PMID24425864
PMCPMC3937697
OpenAlexW2048117958

What OpenQuestion holds

Textmetadata
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.