Evidence map›Paper›PMID 25150689›Full record

ArticleMicrobes and infection2014

Adipocytes in both brown and white adipose tissue of adult mice are functionally connected via gap junctions: implications for Chagas disease.

Shoshana Burke, Fnu Nagajyothi, Mia M Thi, Menachem Hanani, Philipp E Scherer, Herbert B Tanowitz, David C Spray

Open access · greenAbstract read
In one paragraph

Article in Microbes and infection, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

30 citing papers in PubMed, 45 citations in OpenAlex.

  1. Interstitial cells and arrhythmia.American journal of physiology. Cell physiology · 2026
    Review
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  8. Nonmyocytes as electrophysiological contributors to cardiac excitation and conduction.American journal of physiology. Heart and circulatory physiology · 2023
    Review
  9. Unnexin is a protein subunit of a large-pore channel expressed by unicellular organisms.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
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  18. Activation of Cx43 Hemichannels Induces the Generation of CaInternational journal of molecular sciences · 2021
    Article
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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

7 authors at 3 institutions in 2 countries.

Shoshana BurkeDepartment of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Fnu NagajyothiDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Mia M ThiDepartment of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Orthopedic Surgery, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Menachem HananiLaboratory of Experimental Surgery, Hadassah-Hebrew University Medical Center, Mount Scopus, Jerusalem 91120, Israel.
Philipp E SchererDepartment of Internal Medicine and Cell Biology and the Touchstone Diabetes Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Herbert B TanowitzDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
David C SprayDepartment of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA. Electronic address: david.spray@einstein.yu.edu.
Albert Einstein College of Medicine · USHadassah Medical Center · ILThe University of Texas Southwestern Medical Center · US

Funding

Geographic Medicine and Emerging InfectionsT32AI070117 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI WEISS, LOUIS M. · 2008 to 2023
$5.1M
Structural, Molecular, and Functional Specialization in Osteocyte MechanosensingR01AR057139 · NIAMS · CITY COLLEGE OF NEW YORK · PI SCHAFFLER, MITCHELL B, SPRAY, DAVID C · 2010 to 2014
$2.5M
T. cruzi: pathogenesis modulation by eicosanoidsR01AI076248 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI TANOWITZ, HERBERT BERNARD · 2008 to 2012
$2.3M
Effects of High Glucose on Bone Cell Mechanosensing, Transduction, and SignalingR01DK091466 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI THI, MIA M · 2011 to 2015
$1.8M
Role of Lipoproteins in Chagasic heart diseaseR21HL112099 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI NAGAJYOTHI, JYOTHI FALGUNI · 2012 to 2013
$449k
NHLBI NIH HHS HL112099NHLBI NIH HHS R21 HL112099NIAID NIH HHS AI076248NIAID NIH HHS R01 AI076248NIAID NIH HHS T32 AI070117NIAMS NIH HHS AR057139NIAMS NIH HHS R01 AR057139NIDDK NIH HHS DK091466NIDDK NIH HHS R01 DK091466
6 · The paper itself

Abstract

Adipose tissue serves as a host reservoir for the protozoan Trypanosoma cruzi, the causative organism in Chagas disease. Gap junctions interconnect cells of most tissues, serving to synchronize cell activities including secretion in glandular tissue, and we have previously demonstrated that gap junctions are altered in various tissues and cells infected with T. cruzi. Herein, we examined the gap junction protein connexin 43 (Cx43) expression in infected adipose tissues. Adipose tissue is the largest endocrine organ of the body and is also involved in other physiological functions. In mammals, it is primarily composed of white adipocytes. Although gap junctions are a prominent feature of brown adipocytes, they have not been explored extensively in white adipocytes, especially in the setting of infection. Thus, we examined functional coupling in both white and brown adipocytes in mice. Injection of electrical current or the dye Lucifer Yellow into adipocytes within fat tissue spread to adjacent cells, which was reduced by treatment with agents known to block gap junctions. Moreover, Cx43 was detected in both brown and white fat tissue. At thirty and ninety days post-infection, Cx43 was downregulated in brown adipocytes and upregulated in white adipocytes. Gap junction-mediated intercellular communication likely contributes to hormone secretion and other functions in white adipose tissue and to nonshivering thermogenesis in brown fat, and modulation of the coupling by T. cruzi infection is expected to impact these functions.

Indexed as

Cell CommunicationAdipocytes, BrownAdipocytes, WhiteAnimalsChagas DiseaseConnexin 43Disease Models, AnimalGap JunctionsGene Expression ProfilingHost-Pathogen InteractionsMaleMiceTrypanosoma cruziConnexin 43GJA1 protein, mouseAdipose tissueChagas diseaseConnexin43Gap junctionsTrypanosoma cruzi

Identifiers

PMID25150689
PMCPMC4353925
OpenAlexW2071113170

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.