Evidence map›Paper›PMID 27623388›Full record

ArticleJournal of diabetes and its complications2017

Imbalance between HDAC and HAT activities drives aberrant STAT1/MyD88 expression in macrophages from type 1 diabetic mice.

Luciano Ribeiro Filgueiras, Stephanie L Brandt, Theresa Raquel de Oliveira Ramalho, Sonia Jancar, C Henrique Serezani

Open access · greenAbstract read
In one paragraph

Article in Journal of diabetes and its complications, 2017. 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
0.6field-weighted citation impact, top 30% 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, 26 citations in OpenAlex.

  1. Article
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  4. Sex-specific epigenetic programming in renal fibrosis and inflammation.American journal of physiology. Renal physiology · 2023
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  11. Epigenetic Control of a Local Chromatin Landscape.International journal of molecular sciences · 2020
    Review
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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

5 authors at 2 institutions in 2 countries.

Luciano Ribeiro FilgueirasDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP 05508, Brazil. Electronic address: luciano.ribeiro@usp.br.
Stephanie L BrandtDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Theresa Raquel de Oliveira RamalhoDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP 05508, Brazil.
Sonia JancarDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP 05508, Brazil.
C Henrique SerezaniDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Universidade de São Paulo · BRIndiana University – Purdue University Indianapolis · US

Funding

Translation CoreP30DK097512 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Carmella Evans-Molina · 2015 to 2026
$17.4M
Phosphatase and tensin homolog PTEN actions in polymicrobial sepsisR01HL124159 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SEREZANI, C. HENRIQUE · 2014 to 2022
$4.2M
Regulation of Toll-like receptor-induced NFkB activation by Gai-coupled receptorsR00HL103777 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI SEREZANI, C. HENRIQUE · 2012 to 2014
$713k
Regulation of Toll-like receptor-induced NFkB activation by Gai-coupled receptorsK99HL103777 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SEREZANI, C. HENRIQUE · 2010 to 2011
$242k
LTB4 and the control of methicilin resistant Staphylococcus aureus infectionR03AI110990 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI SEREZANI, C. HENRIQUE · 2015 to 2016
$156k
NHLBI NIH HHS K99 HL103777NHLBI NIH HHS R00 HL103777NHLBI NIH HHS R01 HL124159NIAID NIH HHS R03 AI110990NIDDK NIH HHS P30 DK097512
6 · The paper itself

Abstract

aimsTo investigate the hypothesis that alteration in histone acetylation/deacetylation triggers aberrant STAT1/MyD88 expression in macrophages from diabetics. Increased STAT1/MyD88 expression is correlated with sterile inflammation in type 1 diabetic (T1D) mice.

methodsTo induce diabetes, we injected low-doses of streptozotocin in C57BL/6 mice. Peritoneal or bone marrow-differentiated macrophages were cultured in 5mM (low) or 25mM (high glucose). ChIP analysis of macrophages from nondiabetic or diabetic mice was performed to determine acetylation of lysine 9 in histone H3 in MyD88 and STAT1 promoter regions. Macrophages from diabetic mice were treated with the histone acetyltransferase inhibitor anacardic acid (AA), followed by determination of mRNA expression by qPCR.

resultsIncreased STAT1 and MyD88 expression in macrophages from diabetic but not naive mice cultured in low glucose persisted for up to 6days. Macrophages from diabetic mice exhibited increased activity of histone acetyltransferases (HAT) and decreased histone deacetylases (HDAC) activity. We detected increased H3K9Ac binding to Stat1/Myd88 promoters in macrophages from T1D mice and AA in vitro treatment reduced STAT1 and MyD88 mRNA expression. CONCLUSIONS/

interpretationThese results indicate that histone acetylation drives elevated Stat1/Myd88 expression in macrophages from diabetic mice, and this mechanism may be involved in sterile inflammation and diabetes comorbidities.

Indexed as

Gene Expression RegulationAcetylationAnimalsBone Marrow CellsCells, CulturedDiabetes Mellitus, Type 1Enzyme InhibitorsEpigenesis, GeneticGlucoseHistone AcetyltransferasesHistone DeacetylasesHistonesMacrophagesMacrophages, PeritonealMaleMice, Inbred C57BLEnzyme InhibitorsGlucoseHistone AcetyltransferasesHistone DeacetylasesHistonesMyd88 protein, mouseMyeloid Differentiation Factor 88Stat1 protein, mouseSTAT1 Transcription FactorStreptozocinDiabetesEpigeneticHistone acetylationInflammationMacrophageMetabolic memory

Identifiers

PMID27623388
PMCPMC5296405
OpenAlexW2505231718

What OpenQuestion holds

Textmetadata
LicenceTDM
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.