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Dysregulated cellular metabolism in atherosclerosis: mediators and therapeutic opportunities.
Stroope, Chad; Nettersheim, Felix Sebastian; Coon, Brian; Finney, Alexandra C; Schwartz, Martin A; Ley, Klaus; Rom, Oren; Yurdagul, Arif.
Afiliação
  • Stroope C; Department of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, LA, USA.
  • Nettersheim FS; La Jolla Institute for Immunology, La Jolla, CA, USA.
  • Coon B; Department of Cardiology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
  • Finney AC; Yale Cardiovascular Research Center, Division of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
  • Schwartz MA; Cardiovascular Biology Research Program, OMRF, Oklahoma City, OK, USA.
  • Ley K; Department of Cell Biology, Oklahoma University Health Sciences Center, Oklahoma City, OK, USA.
  • Rom O; Department of Pathology and Translational Pathobiology, Louisiana State University Health Sciences Center, Shreveport, LA, USA.
  • Yurdagul A; Yale Cardiovascular Research Center, Division of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
Nat Metab ; 6(4): 617-638, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38532071
ABSTRACT
Accumulating evidence over the past decades has revealed an intricate relationship between dysregulation of cellular metabolism and the progression of atherosclerotic cardiovascular disease. However, an integrated understanding of dysregulated cellular metabolism in atherosclerotic cardiovascular disease and its potential value as a therapeutic target is missing. In this Review, we (1) summarize recent advances concerning the role of metabolic dysregulation during atherosclerosis progression in lesional cells, including endothelial cells, vascular smooth muscle cells, macrophages and T cells; (2) explore the complexity of metabolic cross-talk between these lesional cells; (3) highlight emerging technologies that promise to illuminate unknown aspects of metabolism in atherosclerosis; and (4) suggest strategies for targeting these underexplored metabolic alterations to mitigate atherosclerosis progression and stabilize rupture-prone atheromas with a potential new generation of cardiovascular therapeutics.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aterosclerose Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aterosclerose Idioma: En Ano de publicação: 2024 Tipo de documento: Article