Transglutaminase 2 as a therapeutic target for neurological conditions.

Alzheimer’s disease CNS injury Huntington’s disease Parkinson’s disease TG2 inhibitors Transglutaminase 2 multiple sclerosis neurodegenerative diseases

Journal

Expert opinion on therapeutic targets
ISSN: 1744-7631
Titre abrégé: Expert Opin Ther Targets
Pays: England
ID NLM: 101127833

Informations de publication

Date de publication:
09 2021
Historique:
pubmed: 6 10 2021
medline: 3 3 2022
entrez: 5 10 2021
Statut: ppublish

Résumé

Transglutaminase 2 (TG2) has been implicated in numerous neurological conditions, including neurodegenerative diseases, multiple sclerosis, and CNS injury. Early studies on the role of TG2 in neurodegenerative conditions focused on its ability to 'crosslink' proteins into insoluble aggregates. However, more recent studies have suggested that this is unlikely to be the primary mechanism by which TG2 contributes to the pathogenic processes. Although the specific mechanisms by which TG2 is involved in neurological conditions have not been clearly defined, TG2 regulates numerous cellular processes through which it could contribute to a specific disease. Given the fact that TG2 is a stress-induced gene and elevated in disease or injury conditions, TG2 inhibitors may be useful neurotherapeutics. Overview of TG2 and different TG2 inhibitors. A brief review of TG2 in neurodegenerative diseases, multiple sclerosis and CNS injury and inhibitors that have been tested in different models. Database search: https://pubmed.ncbi.nlm.nih.gov prior to 1 July 2021. Currently, it appears unlikely that inhibiting TG2 in the context of neurodegenerative diseases would be therapeutically advantageous. However, for multiple sclerosis and CNS injuries, TG2 inhibitors may have the potential to be therapeutically useful and thus there is rationale for their further development.

Identifiants

pubmed: 34607527
doi: 10.1080/14728222.2021.1989410
doi:

Substances chimiques

Protein Glutamine gamma Glutamyltransferase 2 EC 2.3.2.13
Transglutaminases EC 2.3.2.13
GTP-Binding Proteins EC 3.6.1.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

721-731

Subventions

Organisme : NINDS NIH HHS
ID : R21 NS119673
Pays : United States
Organisme : CIHR
ID : PJT-162180
Pays : Canada

Auteurs

Jeffrey W Keillor (JW)

Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, ON, Canada.

Gail V W Johnson (GVW)

Department of Anesthesiology and Perioperative Medicine, University of Rochester, Rochester, NY, USA.

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Classifications MeSH