Mc. Cheung et al., PLASMA PHOSPHOLIPID MASS-TRANSFER RATE - RELATIONSHIP TO PLASMA PHOSPHOLIPID AND CHOLESTERYL ESTER TRANSFER ACTIVITIES AND LIPID PARAMETERS, Biochimica et biophysica acta, L. Lipids and lipid metabolism, 1303(2), 1996, pp. 103-110
Human plasma phospholipid transfer protein (PLTP) has been shown to fa
cilitate the transfer of phospholipid from liposomes or isolated very
low and low density lipoproteins to high density lipoproteins. Its act
ivity in plasma and its physiological function are presently unknown.
To elucidate the role of PLTP in lipoprotein metabolism and to delinea
te factors that may affect the rate of phospholipid transfer between l
ipoproteins, we determined the plasma phospholipid mass transfer rate
(PLTR) in 16 healthy adult volunteers and assessed its relationship to
plasma lipid levels, and to phospholipid transfer activity (PLTA) and
cholesteryl ester transfer activity (CETA) measured by radioassays. T
he plasma PLTR in these subjects was 27.2 +/- 11.8 nmol/ml per h at 37
degrees C (mean +/- S.D.), and their PLTA and CETA were 13.0 +/- 1.7
mu mol/ml per h and 72.8 +/- 15.7 nmol/ml per h, respectively. Plasma
PLTR was correlated directly with total, non-HDL, and HDL triglyceride
(r(s) = 0.76, P < 0.001), total and non-HDL phospholipid (r(s), > 0.5
3, P < 0.05), and inversely with HDL free cholesterol (r(s) = -0.54, P
< 0.05), but not with plasma PLTA and CETA. When 85% to 96% of the PL
TA in plasma was removed by polyclonal antibodies against recombinant
human PLTP-phospholipid mass transfer from VLDL and LDL to HDL was red
uced by 50% to 72%, but 80% to 100% of CETA could still be detected. T
hese studies demonstrate that PLTP plays a major role in facilitating
the transfer of phospholipid between lipoproteins, and suggest that tr
iglyceride is a significant modulator of intravascular phospholipid tr
ansport. Furthermore, most of the PLTP and CETP in human plasma is ass
ociated with different particles. Plasma PLTA and CETA were also measu
red in mouse, rat, hamster, guinea pig, rabbit, dog, pig, and monkey.
Compared to human, PLTA in rat and mouse was significantly higher and
in rabbit and guinea pig was significantly lower while the remaining a
nimal species had PLTA similar to humans. No correlation between PLTA
and CETA was observed among animal species.