Key result
ABCA1 drives nascent HDL biogenesis via membrane remodeling, apoAI unfolding, and subsequent lipidation.
Answers are grounded in this paper and cite their sources.
ABCA1 mediates the secretion of cellular free cholesterol and phospholipids to an extracellular acceptor, apolipoprotein AI, to form nascent high-density lipoprotein (HDL). Thus, ABCA1 is a key molecule in cholesterol homeostasis. Functional studies of certain Tangier disease mutations demonstrate that ABCA1 has multiple activities, including plasma membrane remodeling and apoAI binding to cell surface, which participate in nascent HDL biogenesis. Recent advances in our understanding of ABCA1 have demonstrated that ABCA1also mediates unfolding the N terminus of apoAI on the cell surface, followed by lipidation of apoAI and release of nascent HDL. Although ABCA1-mediated cholesterol efflux to apoAI can occur on the plasma membrane, the role of apoAI retroendocytosis during cholesterol efflux may play a role in macrophage foam cells that store cholesterol esters in cytoplasmic lipid droplets.
No takes yet. Share an insight, caveat, or question.
Wang et al. (2014) conducted a review in Tangier disease. ABCA1 mediates nascent HDL biogenesis through plasma membrane remodeling, cell-surface apoAI binding and N-terminal unfolding, and subsequent apoAI lipidation.
Synapse has enriched 10 related papers. Consider them for comparative context: