Unlocking the mysteries of VLDL: exploring its production, intracellular trafficking, and metabolism as therapeutic targets

Lipids Health Dis. 2024 Jan 12;23(1):14. doi: 10.1186/s12944-023-01993-y.

Abstract

Reducing circulating lipid levels is the centerpiece of strategies for preventing and treating atherosclerotic cardiovascular disease (ASCVD). Despite many available lipid-lowering medications, a substantial residual cardiovascular risk remains. Current clinical guidelines focus on plasma levels of low-density lipoprotein (LDL). Recent attention has been given to very low-density lipoprotein (VLDL), the precursor to LDL, and its role in the development of coronary atherosclerosis. Preclinical investigations have revealed that interventions targeting VLDL production or promoting VLDL metabolism, independent of the LDL receptor, can potentially decrease cholesterol levels and provide therapeutic benefits. Currently, methods, such as mipomersen, lomitapide, and ANGPTL3 inhibitors, are used to reduce plasma cholesterol and triglyceride levels by regulating the lipidation, secretion, and metabolism of VLDL. Targeting VLDL represents an avenue for new lipid-lowering strategies. Interventions aimed at reducing VLDL production or enhancing VLDL metabolism, independent of the LDL receptor, hold promise for lowering cholesterol levels and providing therapeutic benefits beyond LDL in the management of ASCVD.

Keywords: Atherosclerotic cardiovascular disease; LDL receptor-independent pathway; Low-density lipoprotein; Very low-density lipoprotein.

MeSH terms

  • Angiopoietin-Like Protein 3
  • Atherosclerosis*
  • Cholesterol
  • Humans
  • Lipoproteins, LDL
  • Lipoproteins, VLDL*
  • Receptors, LDL / genetics

Substances

  • Lipoproteins, VLDL
  • Lipoproteins, LDL
  • Receptors, LDL
  • Cholesterol
  • ANGPTL3 protein, human
  • Angiopoietin-Like Protein 3