Evidence map›Paper›PMID 31914588›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2020

Glycolysis regulated transglutaminase 2 activation in cardiopulmonary fibrogenic remodeling.

Chinmayee D Bhedi, Sabina Nasirova, Deniz Toksoz, Rod R Warburton, Kevin J Morine, Navin K Kapur, Jonas B Galper, Ioana R Preston, Nicholas S Hill, Barry L Fanburg and 1 more

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 43 citations in OpenAlex.

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  12. Role of Pyruvate Kinase M2 (PKM2) in Cardiovascular Diseases.Journal of cardiovascular translational research · 2023
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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

11 authors at 1 institution in 1 country.

Chinmayee D BhediPulmonary Division, Department of Medicine, Tufts Medical Center, Boston, MA, USA.
Sabina NasirovaPulmonary Division, Department of Medicine, Tufts Medical Center, Boston, MA, USA.
Deniz ToksozPulmonary Division, Department of Medicine, Tufts Medical Center, Boston, MA, USA.
Rod R WarburtonPulmonary Division, Department of Medicine, Tufts Medical Center, Boston, MA, USA.
Kevin J MorineMolecular Cardiology Research Institute, Tufts Medical Center, Boston, MA, USA.
Navin K KapurMolecular Cardiology Research Institute, Tufts Medical Center, Boston, MA, USA.
Jonas B GalperMolecular Cardiology Research Institute, Tufts Medical Center, Boston, MA, USA.
Ioana R PrestonPulmonary Division, Department of Medicine, Tufts Medical Center, Boston, MA, USA.
Nicholas S HillPulmonary Division, Department of Medicine, Tufts Medical Center, Boston, MA, USA.
Barry L FanburgPulmonary Division, Department of Medicine, Tufts Medical Center, Boston, MA, USA.
Krishna C PenumatsaPulmonary Division, Department of Medicine, Tufts Medical Center, Boston, MA, USA.
Tufts Medical Center · US

Funding

Role of Sterols &Insulin in Cardiac Autonomic ResponseR01HL074876 · NHLBI · TUFTS MEDICAL CENTER · PI GALPER, JONAS BERNARD · 2004 to 2013
$3.2M
Smooth Muscle Cell Protein Serotonylation and Pulmonary HypertensionR01HL107713 · NHLBI · TUFTS MEDICAL CENTER · PI FANBURG, BARRY · 2012 to 2015
$1.9M
NHLBI NIH HHS R01 HL074876NHLBI NIH HHS R01 HL107713
6 · The paper itself

Abstract

The pathophysiology of pulmonary hypertension (PH) and heart failure (HF) includes fibrogenic remodeling associated with the loss of pulmonary arterial (PA) and cardiac compliance. We and others have previously identified transglutaminase 2 (TG2) as a participant in adverse fibrogenic remodeling. However, little is known about the biologic mechanisms that regulate TG2 function. We examined physiological mouse models of experimental PH, HF, and type 1 diabetes that are associated with altered glucose metabolism/glycolysis and report here that TG2 expression and activity are elevated in pulmonary and cardiac tissues under all these conditions. We additionally used PA adventitial fibroblasts to test the hypothesis that TG2 is an intermediary between enhanced tissue glycolysis and fibrogenesis. Our in vitro results show that glycolytic enzymes and TG2 are upregulated in fibroblasts exposed to high glucose, which stimulates cellular glycolysis as measured by Seahorse analysis. We examined the relationship of TG2 to a terminal glycolytic enzyme, pyruvate kinase M2 (PKM2), and found that PKM2 regulates glucose-induced TG2 expression and activity as well as fibrogenesis. Our studies further show that TG2 inhibition blocks glucose-induced fibrogenesis and cell proliferation. Our findings support a novel role for glycolysis-mediated TG2 induction and tissue fibrosis associated with experimental PH, HF, and hyperglycemia.

Indexed as

Gene Expression Regulation, EnzymologicGlycolysisAnimalsCarrier ProteinsCell ProliferationFibroblastsGlucoseGTP-Binding ProteinsHumansHyperglycemiaHypertension, PulmonaryMembrane ProteinsMiceMice, Inbred C57BLProtein Glutamine gamma Glutamyltransferase 2Pulmonary ArteryCarrier ProteinsGlucoseGTP-Binding ProteinsMembrane ProteinsPkm protein, mouseProtein Glutamine gamma Glutamyltransferase 2Pyruvate KinaseThyroid Hormone-Binding ProteinsThyroid Hormonestransglutaminase 1TransglutaminasesglycolysishyperglycemiaPKM2TG2tissue fibrosis

Identifiers

PMID31914588
PMCPMC6956703
OpenAlexW2991303513

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.