TY - JOUR
T1 - Plasma membrane lipids
T2 - An important binding site for all lipoprotein classes
AU - Axmann, Markus
AU - Plochberger, Birgit
AU - Mikula, Mario
AU - Weber, Florian
AU - Strobl, Witta Monika
AU - Stangl, Herbert
N1 - Funding Information:
Funding: Open Access Funding by the Austrian Science Fund (FWF). Instruct-CZ Centre supported by MEYS CR (LM2018127), Mario Mikula is supported by the Austrian Science Fund project P 32979-B. Markus Axmann and Florian Weber are supported by the Austrian Science Fund project P 33481-B.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/11/17
Y1 - 2021/11/17
N2 - Cholesterol is one of the main constituents of plasma membranes; thus, its supply is of utmost importance. This review covers the known mechanisms of cholesterol transfer from circulating lipoprotein particles to the plasma membrane, and vice versa. To achieve homeostasis, the human body utilizes cellular de novo synthesis and extracellular transport particles for supply of cholesterol and other lipids via the blood stream. These lipoprotein particles can be classified according to their density: chylomicrons, very low, low, and high-density lipoprotein (VLDL, LDL, and HDL, respectively). They deliver and receive their lipid loads, most importantly cholesterol, to and from cells by several redundant routes. Defects in one of these pathways (e.g., due to mutations in receptors) usually are not immediately fatal. Several redundant pathways, at least temporarily, compensate for the loss of one or more of them, but the defects trigger systemic diseases, such as atherosclerosis later on. Recently, intracellular membrane–membrane contact sites were shown to be involved in intracellular cholesterol transfer and the plasma membrane itself has been proposed to act as a binding site for lipoprotein-mediated cargo unloading.
AB - Cholesterol is one of the main constituents of plasma membranes; thus, its supply is of utmost importance. This review covers the known mechanisms of cholesterol transfer from circulating lipoprotein particles to the plasma membrane, and vice versa. To achieve homeostasis, the human body utilizes cellular de novo synthesis and extracellular transport particles for supply of cholesterol and other lipids via the blood stream. These lipoprotein particles can be classified according to their density: chylomicrons, very low, low, and high-density lipoprotein (VLDL, LDL, and HDL, respectively). They deliver and receive their lipid loads, most importantly cholesterol, to and from cells by several redundant routes. Defects in one of these pathways (e.g., due to mutations in receptors) usually are not immediately fatal. Several redundant pathways, at least temporarily, compensate for the loss of one or more of them, but the defects trigger systemic diseases, such as atherosclerosis later on. Recently, intracellular membrane–membrane contact sites were shown to be involved in intracellular cholesterol transfer and the plasma membrane itself has been proposed to act as a binding site for lipoprotein-mediated cargo unloading.
KW - HDL
KW - LDL
KW - Lipoprotein particles
KW - Non-esterified cholesterol
KW - Plasma membrane
UR - http://www.scopus.com/inward/record.url?scp=85119718366&partnerID=8YFLogxK
U2 - 10.3390/membranes11110882
DO - 10.3390/membranes11110882
M3 - Review article
C2 - 34832111
SN - 2077-0375
VL - 11
JO - Membranes
JF - Membranes
IS - 11
M1 - 882
ER -