| Literature DB >> 33504179 |
Jedrzej Hoffmann1, Gavin Richardson2, Judith Haendeler3, Joachim Altschmied3,4, Vicente Andrés5,6, Ioakim Spyridopoulos7,8.
Abstract
Shortened telomeres have been linked to numerous chronic diseases, most importantly coronary artery disease, but the underlying mechanisms remain ill defined. Loss-of-function mutations and deletions in telomerase both accelerate telomere shortening but do not necessarily lead to a clinical phenotype associated with atherosclerosis, questioning the causal role of telomere length in cardiac pathology. The differential extranuclear functions of the 2 main components of telomerase, telomerase reverse transcriptase and telomerase RNA component, offer important clues about the complex relationship between telomere length and cardiovascular pathology. In this review, we critically discuss relevant preclinical models, genetic disorders, and clinical studies to elucidate the impact of telomerase in cardiovascular disease and its potential role as a therapeutic target. We suggest that the antioxidative function of mitochondrial telomerase reverse transcriptase might be atheroprotective, making it a potential target for clinical trials. Graphic Abstract: A graphic abstract is available for this article.Entities:
Keywords: T-lymphocytes; aging; atherosclerosis; cardiovascular diseases; oxidative stress; telomerase; telomere
Mesh:
Substances:
Year: 2021 PMID: 33504179 DOI: 10.1161/ATVBAHA.120.315695
Source DB: PubMed Journal: Arterioscler Thromb Vasc Biol ISSN: 1079-5642 Impact factor: 8.311