Literature DB >> 35817809

Protein O-GlcNAcylation in cardiovascular diseases.

Hui-Fang Wang1, Yi-Xuan Wang1, Yu-Ping Zhou2, Yun-Peng Wei2, Yi Yan3,4, Ze-Jian Zhang5, Zhi-Cheng Jing6.   

Abstract

O-GlcNAcylation is a post-translational modification of protein in response to genetic variations or environmental factors, which is controlled by two highly conserved enzymes, i.e. O-GlcNAc transferase (OGT) and protein O-GlcNAcase (OGA). Protein O-GlcNAcylation mainly occurs in the cytoplasm, nucleus, and mitochondrion, and it is ubiquitously implicated in the development of cardiovascular disease (CVD). Alterations of O-GlcNAcylation could cause massive metabolic imbalance and affect cardiovascular function, but the role of O-GlcNAcylation in CVD remains controversial. That is, acutely increased O-GlcNAcylation is an adaptive heart response, which temporarily protects cardiac function. While it is harmful to cardiomyocytes if O-GlcNAcylation levels remain high in chronic conditions or in the long run. The underlying mechanisms include regulation of transcription, energy metabolism, and other signal transduction reactions induced by O-GlcNAcylation. In this review, we will focus on the interactions between protein O-GlcNAcylation and CVD, and discuss the potential molecular mechanisms that may be able to pave a new avenue for the treatment of cardiovascular events.
© 2022. The Author(s), under exclusive licence to Shanghai Institute of Materia Medica, Chinese Academy of Sciences and Chinese Pharmacological Society.

Entities:  

Keywords:  O-GlcNAcylation; cardiovascular disease; glycomics; glycosylation

Year:  2022        PMID: 35817809     DOI: 10.1038/s41401-022-00934-2

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   7.169


  115 in total

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Journal:  Nat Rev Mol Cell Biol       Date:  2012-06-22       Impact factor: 94.444

2.  cDNA cloning and mapping of a novel subtype of glutamine:fructose-6-phosphate amidotransferase (GFAT2) in human and mouse.

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3.  Topography and polypeptide distribution of terminal N-acetylglucosamine residues on the surfaces of intact lymphocytes. Evidence for O-linked GlcNAc.

Authors:  C R Torres; G W Hart
Journal:  J Biol Chem       Date:  1984-03-10       Impact factor: 5.157

4.  Modulation of dynamin-related protein 1 (DRP1) function by increased O-linked-β-N-acetylglucosamine modification (O-GlcNAc) in cardiac myocytes.

Authors:  Thomas Gawlowski; Jorge Suarez; Brian Scott; Moises Torres-Gonzalez; Hong Wang; Raphaela Schwappacher; Xuemei Han; John R Yates; Masahiko Hoshijima; Wolfgang Dillmann
Journal:  J Biol Chem       Date:  2012-06-28       Impact factor: 5.157

Review 5.  The hexosamine signaling pathway: O-GlcNAc cycling in feast or famine.

Authors:  John A Hanover; Michael W Krause; Dona C Love
Journal:  Biochim Biophys Acta       Date:  2009-07-30

Review 6.  O-linked beta-N-acetylglucosamine (O-GlcNAc): Extensive crosstalk with phosphorylation to regulate signaling and transcription in response to nutrients and stress.

Authors:  Chutikarn Butkinaree; Kyoungsook Park; Gerald W Hart
Journal:  Biochim Biophys Acta       Date:  2009-08-06

7.  Molecular cloning, cDNA sequence, and bacterial expression of human glutamine:fructose-6-phosphate amidotransferase.

Authors:  G L McKnight; S L Mudri; S L Mathewes; R R Traxinger; S Marshall; P O Sheppard; P J O'Hara
Journal:  J Biol Chem       Date:  1992-12-15       Impact factor: 5.157

Review 8.  Glucose Metabolism in Cardiac Hypertrophy and Heart Failure.

Authors:  Diem H Tran; Zhao V Wang
Journal:  J Am Heart Assoc       Date:  2019-06-12       Impact factor: 5.501

9.  First characterization of glucose flux through the hexosamine biosynthesis pathway (HBP) in ex vivo mouse heart.

Authors:  Aaron K Olson; Bertrand Bouchard; Wei Zhong Zhu; John C Chatham; Christine Des Rosiers
Journal:  J Biol Chem       Date:  2020-01-08       Impact factor: 5.157

Review 10.  Global Burden of Cardiovascular Diseases and Risk Factors, 1990-2019: Update From the GBD 2019 Study.

Authors:  Gregory A Roth; George A Mensah; Catherine O Johnson; Giovanni Addolorato; Enrico Ammirati; Larry M Baddour; Noël C Barengo; Andrea Z Beaton; Emelia J Benjamin; Catherine P Benziger; Aimé Bonny; Michael Brauer; Marianne Brodmann; Thomas J Cahill; Jonathan Carapetis; Alberico L Catapano; Sumeet S Chugh; Leslie T Cooper; Josef Coresh; Michael Criqui; Nicole DeCleene; Kim A Eagle; Sophia Emmons-Bell; Valery L Feigin; Joaquim Fernández-Solà; Gerry Fowkes; Emmanuela Gakidou; Scott M Grundy; Feng J He; George Howard; Frank Hu; Lesley Inker; Ganesan Karthikeyan; Nicholas Kassebaum; Walter Koroshetz; Carl Lavie; Donald Lloyd-Jones; Hong S Lu; Antonio Mirijello; Awoke Misganaw Temesgen; Ali Mokdad; Andrew E Moran; Paul Muntner; Jagat Narula; Bruce Neal; Mpiko Ntsekhe; Glaucia Moraes de Oliveira; Catherine Otto; Mayowa Owolabi; Michael Pratt; Sanjay Rajagopalan; Marissa Reitsma; Antonio Luiz P Ribeiro; Nancy Rigotti; Anthony Rodgers; Craig Sable; Saate Shakil; Karen Sliwa-Hahnle; Benjamin Stark; Johan Sundström; Patrick Timpel; Imad M Tleyjeh; Marco Valgimigli; Theo Vos; Paul K Whelton; Magdi Yacoub; Liesl Zuhlke; Christopher Murray; Valentin Fuster
Journal:  J Am Coll Cardiol       Date:  2020-12-22       Impact factor: 24.094

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