Open Access

Plasma PLTP activity is inversely associated with HDL-C levels

Contributed equally
Nutrition & Metabolism20096:49

https://doi.org/10.1186/1743-7075-6-49

Received: 3 August 2009

Accepted: 30 November 2009

Published: 30 November 2009

Abstract

Phospholipid transfer protein (PLTP) is an important modulator of lipoprotein metabolism, including interparticle phospholipid transfer, remodeling of HDL, cholesterol and phospholipid efflux from peripheral tissues, and the production of hepatic VLDL. PLTP also plays an important role in inflammation and oxidative stress. Accordingly, PLTP has been implicated in the development of atherosclerosis. In this study, we evaluated the association between PLTP activity and lipoprotein metabolism in a Chinese patients cohort with or without coronary heart disease (CHD group n = 407, control group n = 215), the PLTP activity was measured and PLTP genotyping was screened for sequence anomalies by PCR. We found that human plasma PLTP activity was negatively associated with plasma HDL and apoA-I levels, and positively associated with plasma TG, apoB and apoE levels. We also found that PLTP rs2294213 polymorphism was tended to be associated with increased plasma PLTP activity.

Plasma phospholipid transfer protein (PLTP) is a lipid transfer glycoprotein that binds to and transfers a number of compounds including phospholipids, diacylglycerides, unesterified cholesterol, and lipopolysaccharidesl. In humans, PLTP activity has been shown to be positively and independently related to coronary heart disease (CHD) [1] In addition, previous studies showed that PLTP activity was increased with aging [2], obesity [3, 4], type 1 and type 2 diabetes [46]. It is known that PLTP is involved in high-density-lipoprotein (HDL) metabolism in that human plasma PLTP activity was either positively [7, 8] or negatively[2, 9] correlated with HDL levels in various patient populations.

PLTP deficiency has not been found in humans while numerous PLTP polymorphisms were identified. Tahvanainen et al. reported 6 PLTP intragenic polymorphisms: c.-79G>T, c. -56G>A, c.-37T>C, c.-31A>G, p.Phe2Leu, Arg121Trp, and 2 neutral polymorphisms, however, there were no significant associations between these polymorphisms and plasma PLTP activity[2]. Similarly, Bossé and coworkers identified 2 intronic variants of the PLTP gene, 1 in intron 1 (c.-87G>A) and the other in intron 12 (c.1175+68T>G)[10]. Although both of these polymorphisms were associated with obesity-related phenotypes but there was still no significant associations between these polymorphisms and plasma PLTP activity [10]. Aouizerat and colleagues observed p.R235W mutation but not p.E72G, p.S119A, and p.S124Y in the PLTP codon region was related to decreased plasma PLTP activity and c.-34G>C allele was associated with higher HDL-C [11]. It was also reported that possession of the rs2294213 minor allele could increase HDL-C independent of triglycerides[12], but it remains unknown whether this polymorphism could influence PLTP activity and is linked with coronary heart disease(CHD) or not. In the present study, we confirmed the PLTP polymorphism (rs2294213) in a Chinese population and evaluate its relationship with plasma PLTP activity, lipid profiles and CHD.

Methods

Study Population

A total of 622 subjects underwent diagnostic coronary angiography for chest pain in Zhongshan Hospital between 2004 and 2005 were included in this study. Cardiovascular risk factors/diseases were obtained by clinical history. Coronary artery disease (CHD) (n = 407) was diagnosed with the presence of a stenosis ≥50% in at least 1 major coronary artery territory (left anterior descending, left circumflex or right coronary artery). Subjects who had <50% stenosis in any coronary artery served as the controls (n = 215). Exclusion criteria were evidence of significant concomitant cardiac and non-cardiac disease including severe valvular heart disease, known cardiomyopathy, malignancy, or febrile condition. Diabetes mellitus was diagnosed by clinical history, use of hypoglycemic medications or a fasting blood sugar level >7.0 mmol/L (125 mg/dL); hypertension was defined in patients receiving antihypertensive treatment or with known diagnosis of hypertension (blood pressure ≥140/90 mmHg). The study was approved by the Institutional Review Boards of Fudan University.

Laboratory Evaluation

Subjects were advised to fast for at least 8 hours prior to blood sampling. Lipid profile was determined with Hitachi 7600 biochemistry autoanalyzer. Triglyceride (TG), total cholesterol (TC) and high-density lipoprotein-cholesterol (HDL-C) were measured with enzymatic methods (TG, Shanghai Kehuadongling Diagnostics Co., Ltd.; TC, Shanghai Kehuadongling Diagnostics Co., Ltd.; HDL-C, PEG-modified enzyme HDL-C assay, Kyowa Medex Co.). Low-density lipoprotein-cholesterol (LDL-C) was calculated according to the Friedewald formula. ApoA-I, apoE, apoB, and Lipoprotein(a) [Lp(a)] were determined by immunoturbidimetric assays (apoA-I, apo E, and apo B, DiaSyA Diagnostics; Lp(a), Nittobo Boseki Co. Ltd).

PLTP Genotyping

PLTP genotype was identified for each subject by genomic DNA PCR using sense primer TAAAGGCGGCTGGAACAACCCTG-3' and anti-sense primer GCGTTCTCCTTCATCGGCTCT-3'. The SNP reference number was identified by placing the flanking sequences with 30 base paires from each side of the SNP into the NCBI SNP database to do BLAST analysis. The polymorphism (rs2294213) is located on PLTP gene Intron 1.

PLTP Activity Assay

PLTP activity was measured with an assay kit (Cardiovascular Targets Inc., New York, NY, USA). The kit includes both donor and acceptor particles. Incubation of donor and acceptor particles with 3 μl of human plasma results in PLTP-mediated transfer of fluorescent phospholipid, which is present in a self-quenched state when associated with the donor. The transfer is determined by the increase in fluorescence intensity as the fluorescent lipid is removed from the donor and transferred to the acceptor. The interassay coefficient of variation of the PLTP activity was 3.3 ± 0.5%. The linear range of PLTP activity in this assay was between 1 and 7 μl of plasma. Three freeze-thaw cycles of plasma did not influence the assay. To validate the novel PLTP activity assay, we compared the results with those obtained by the classic radiolabeled method [13, 14] There was a high degree of correlation between the 2 methods (r = 0.90, p < 0.01; n = 30). Laboratory personnel were unaware of the study individual assignation.

Statistical Methods

The study subjects were grouped according to their PLTP genotype. Continuous variables were reported as means ± standard deviation (SD) and univariate analysis of variance tests were used to test statistical significance. The Pearson's X2 test statistic was used to assess statistically significant differences in proportions for dichotomous and categorical variables. The distribution of PLTP activity and Lp(a) levels was positively skewed and so were naturally log transformed prior to analyses. Multivariate analysis of variance was performed to evaluate the relationship between PLTP genotype and PLTP activity level. The dependent variable was log transformed PLTP activity level. The independent variables included PLTP genotype, gender, and presence/absence of diabetes, hypertension, smoking, low HDL and CHD. Age and BMI were entered into the model as covariates. Selected interaction effects were tested between the independent variables in the model. Estimated geometric means of PLTP activity level were generated for each independent variable using reverse-log transformation of the ANOVA generated marginal means. LSD test was performed for multiple comparisons. To further investigate the relationship between PLTP activity and plasma lipid parameters, univariate and multivariate linear regression analyses were performed and estimated expected change in PLTP activity was determined for a unit change in each lipid parameter. All analyses were done using SPSS version 17 analytical software (SPSS Inc., Chicago, IL).

Results

Based on genomic DNA PCR and sequence, we detected the rs2294213 PLTP polymorphism which is located on PLTP gene Intron 1. Of the 622 subjects, 277 (44.5%) had 'GG' polymorphism PLTP genotype, 276 (44.4%) had 'CG' PLTP genotype and 69 (11.1%) had 'CC' polymorphism. Obtained genotype frequencies were compared to the calculated frequencies based on the Hardy-Weinberg equilibrium and no significant differences were observed (χ2 = 0.000631, P = 0.980 for all participants; χ2 = 1.443, P = 0.230 for the control group; χ2 = 0.708, P = 0.400 for the CHD patient group). The clinical characteristics of studied patients are shown in Table 1. Age, gender, BMI, and lipid profiles were similar among groups. Prevalence of clinical risk factors including diabetes, hypertension, smoking, low HDL and CHD were also similar among the 3 groups. Plasma PLTP activity was significantly higher in subjects with 'CC' polymorphism than that in subjects with 'GG' and 'GC' polymorphisms (26.7 ± 12.8 pmol/μL/hr vs. 23.7 ± 14.7/24.7 ± 14.0 pmol/μL/hr; p = 0.04). Testing with an LSD test, subjects with 'CC' polymorphism had significantly higher PLTP activity as compared to those with 'GG' one (P = 0.02). However, no statistical significant difference of PLTP activity was found between the 'CC' and 'GC' groups (P = 0.26). The similar result was found between the 'GG' and 'GC' groups (P = 0.07).
Table 1

Patient Characteristics.

Characteristics†

PLTP* genotype (N)

p-value‡

 

gg (277)

gc(276)

cc(69)

 

Age (years)

61.3 ± 10.5

63.3 ± 9.9

63.0 ± 9.4

0.06

Gender

    

   Men (%)

211(76.2)

222(80.4)

54(78.3)

0.64

   Women (%)

65(23.5)

54(19.6)

15(21.7)

 

BMI§ (kg/m2)

24.7 ± 2.9

24.5 ± 2.9

24.5 ± 3.2

0.55

Diabetes (%)

56(20.21)

51(18.5)

11(15.9)

0.69

Hypertension (%)

171(61.7)

175(63.4)

23(33.3)

0.77

Smoking (%)

126(45.5)

133(48.2)

29(42.0)

0.61

CHD|| (%)

176(63.5)

189(68.4)

42(60.8)

0.33

PLTP activity (pmol/μl/h)

23.7 ± 14.7

24.7 ± 14.0

26.7 ± 12.8

0.04

0.02 †† (cc vs gg)

0.26 †† (cc vs gc)

0.07 †† (gg vs gc)

Total-C (mmol/L)

4.71 ± 0.96

4.41 ± 1.03

4.40 ± 0.99

0.74

TG# (mmol/L)

1.74 ± 0.87

1.71 ± 1.08

1.8 ± 0.99

0.79

LDL-C (mmol/L)

2.65 ± 0.85

2.60 ± 0.88

2.55 ± 0.89

0.67

HDL-C (mmol/L)

1.03 ± 0.26

1.04 ± 0.29

1.01 ± 0.27

0.94

Low HDL-C (<0.8 mmol/L) (%)

81(29.2)

80(29.0)

21(30.4)

0.94

LDL-C/HDL-C

2.74 ± 1.28

2.63 ± 0.99

2.71 ± 1.24

0.50

ApoA-I** (g/L)

1.07 ± 0.19

1.06 ± 0.21

1.03 ± 0.21

0.18

apoB (g/L)

0.82 ± 0.42

0.82 ± 0.42

0.79 ± 0.26

0.87

apoE (mg/L)

47.99 ± 25.57

47.34 ± 18.39

45.17 ± 13.00

0.63

Lp(a) (mg/L)

179.76 ± 157.41

202.89 ± 187.61

199.51 ± 227.73

0.30

* PLTP = Phospholipid transfer protein; † Means are presented ± standard deviation; ‡ p-values for differences in means were calculated using t test statistics, p-values for differences in proportions were calculated using Pearson's X2 test, †† p-values for differences using an LSD test for multiple comparisons; § BMI = body mass index; || CHD = Coronary Heart Disease with ≥50% coronary artery stenosis; € compared after log10 transformation; ¶ Cholesterol; # Triglycerides; ** Apolipoprotein.

As shown in Table 2, based on univariate analyses, plasma PLTP activity was significantly associated with male gender, presence of low HDL and with PLTP genotype. In multivariable-adjusted analysis, the effect of gender was attenuated though low HDL and PLTP genotype remained independently associated with PLTP activity.
Table 2

Univariate and multivariate estimates of PLTP activity levels.

Variable

Unadjusted estimated PLTP activity (Mean ± SE)

p-value

Adjusted* estimated PLTP activity (Mean ± SE)

p-value

Gender

    

   Male

21.20 ± 1.03

0.03

24.15 ± 1.06

0.52

   Female

18.27 ± 1.06

 

23.01 ± 1.08

 

Diabetes

    

   Present

22.66 ± 1.06

0.08

24.38 ± 1.07

0.35

   Absent

20.05 ± 1.03

 

22.80 ± 1.05

 

Hypertension

    

   Present

20.13 ± 1.04

0.36

22.86 ± 1.05

0.27

   Absent

21.21 ± 1.05

 

24.38 ± 1.06

 

Smoking

    

   Smoker

21.58 ± 1.04

0.09

24.04 ± 1.07

0.52

   Nonsmoker

21.58 ± 1.04

 

23.12 ± 1.05

 

CHD

    

   Present

20.70 ± 1.03

0.68

23.50 ± 1.05

0.93

   Absent

20.21 ± 1.05

 

23.66 ± 1.07

 

Low HDL-C §

    

   Present

27.20 ± 1.05

<0.01

28.18 ± 1.06

<0.01

   Absent

18.46 ± 1.03

 

19.77 ± 1.05

 

PLTP Polymorphism Type

    

   gg

19.41 ± 1.04

0.03

21.18 ± 1.05

0.03

   cg

21.26 ± 1.04

 

23.50 ± 1.06

 

   cc

23.59 ± 1.09

 

26.36 ± 1.09

 

* Covariates appearing in the multivariate model were evaluated at values of age = 62.43 years and BMI = 25.21 kg/m2; † PLTP= Phospholipid transfer protein; ‡ CHD = Coronary Heart Disease with ≥50% coronary artery stenosis; § Low HDL-C defined as HDL-cholesterol level <0.8 mmol/L.

We next sought to evaluate PLTP activity and its relation with plasma lipid levels. In univariate analysis, PLTP activity was significantly positively associated with plasma triglyceride (TG), apolipoprotein (apo)B and apoE, while it was negatively associated with plasma HDL and apoA-I. The effect of plasma TG was attenuated on multivariable-adjusted analysis (Table 3).
Table 3

Univariate and multivariate plasma lipid correlates of PLTP activity

Predictor variables

Unadjusted expected change in PLTP activity (Units)

p-value

Adjusted† expected change in PLTP† activity (Units)

p-value

Total-Cholesterol, per mmol/L

-1.01

0.06

-1.01

0.05

Triglycerides, per mmol/L

1.03

0.01

-1.00

0.92

HDL-Cholesterol, per mmol/L

-1.15

<0.01

1.27

<0.01

LDL-Cholesterol, per mmol/L

-1.01

0.35

-1.01

0.18

apoA-I, per g/L

-1.48

<0.01

-1.75

<0.01

apoB, per g/L

1.09

<0.01

1.10

<0.01

apoE, per mg/L

1.00

<0.01

1.00

<0.01

Lp(a), per mg/L

1.03

0.29

1.05

0.11

PLTP = Phospholipid transfer protein; † Adjusted for age, gender, BMI, PLTP Polymorphism, and presence or absence of significant CHD.

Discussion

The major finding of our study is that PLTP activity inversely associated with plasma HDL-C levels. Importantly, the significant relation between PLTP activity and HDL-C persisted even after adjustment for age, gender, BMI and presence or absence of significant CHD.

There is growing evidence that the biological role(s) of PLTP is related to HDL metabolism. Transgenic mice that overexpressing human PLTP at high levels were previously been generated. Compared with WT mice, these mice show a 2.5-4.5-fold increase in PLTP activity in plasma [15]. The overexpression of PLTP resulted in a significant decrease of plasma levels of HDL-C[15], increase the formation of preβ-HDL[15], increase catabolism HDL[16, 17], increased atherosclerosis[18], compared with plasma from WT mice. We created PLTP gene knockout (KO) mice[19] which showed a marked decrease in HDL-C, phospholipid, and apoA-I. Furthermore, the HDL of the PLTP KO mice was enriched with protein and poor in phosphatidylcholine, and turnover studies showed a 4-fold increase in the catabolism of HDL protein and CE compared with that of WT mice [20, 21]. Interestingly, both PLTP transgenic and KO mice showed the same phenotype, in terms of HDL levels. These studies could not provide a prediction for the relationship between PLTP activity and HDL levels in humans. Thus far the results from human studies are controversial. Human plasma PLTP activity and HDL levels have been shown to correlate either positively or negatively in different populations [2, 79]. In the present study, we chose a relatively large (n = 622) and relatively uniform cohort and found that, indeed, PLTP activity is inversely related with HDL levels. Why low-HDL subjects with higher PLTP activity? It is known that in addition to promoting transfer of phospholipids from VLDL and chylomicron into HDL[19], PLTP may contribute to the remodelling of HDL particles. PLTP activity contributes to the generation of large HDL as well as small HDL particles [22, 23] and may promote catabolism of these particles, thus decreasing HDL levels. Besides PLTP, there is cholesteryl ester transfer protein (CETP) in human plasma. It is well known that CETP activity is inversely related with HDL[24]. Although PLTP has no CE transfer activity, it can promote CETP activity [25]. We also reported that PLTP KO/CETP transgenic mice have significantly less CETP activity than that in CETP transgenic mice[26]. High PLTP activity might promote CETP activity, thus decreasing HDL levels in human plasma. It is known that PLTP function extends far beyond phospholipid transfer and exchange among lipoproteins. In mice, PLTP deficiency has been associated with a reduction in systemic inflammation [27, 28]. Furthermore, in mouse models, PLTP deficiency has been associated with increased antioxidation potential[29], while the opposite has been observed in PLTP overexpression [30]. In addition, PLTP is also involved in ABCA1-dependent cholesterol efflux, a process which is critical for reverse cholesterol transport [31, 32]. Finally, PLTP activity is closely related to obesity, diabetes mellitus, insulin resistance [36], left ventricular systolic dysfunction [33], and intima-media thickness[34]. Although the mechanism of these associations remains poorly defined, it is likely related to the putative role of PLTP in the development of atherosclerosis, a common underlying factor in each of these disease states.

In this study, we also found PLTP activity is positively related to plasma apoB levels (Table 3). We and other researchers have reported previously that PLTP deficiency in mice results in markedly decreased in apoB-containing lipoproteins in the circulation[35] and PLTP overexpression stimulation of VLDL secretion[36]. This effect may well have an impact on atherogenesis.

In addition, we found a PLTP polymorphism (rs2294213) has impact on PLTP activity. Plasma PLTP activity was higher in subjects with 'CC' polymorphism than that in subjects with 'GG' and 'GC' polymorphisms (26.7 ± 12.8 pmol/μL/hr vs. 23.7 ± 14.7/24.7 ± 14.0 pmol/μL/hr; p = 0.04). However, LSD test showed that except 'CC' vs 'GG' groups, there was no statistical significant difference between the 'CC' and 'GC' or 'GG' and 'GC' groups. Since there were no statistically significant associations between other polymorphisms and plasma PLTP activity [2, 10], the effect of rs2294213 polymorphism on PLTP activity might be marginal.

Engler et al[12] reported that, in non-Hispanic white sample of subjects, allele frequency of rs2294213 accounted for 2.2%, 4.3%, and 7.0% in hypoalphalipoproteinemia, controls, and hyperalphalipoproteinemia groups, respectively, and this polymorphism is responsible for the increasing of HDL-C. However, the allele frequency in our study (33%) is much higher than theirs [12] and we did not observe the effect of this polymorphism on HDL-C levels. The different study population might explain the different allele frequency and different influences towards lipid levels. The relative frequency of the CC polymorphism and its relation to HDL levels merits further study.

We have reported PLTP activity is an independent risk factor for CHD[1], but we do not find the association between PLTP activity and CHD in this Chinese population, which is inconsistent with our precious study in a well-controlled and big size population [1]. This might be related to the relatively small number of patients with normal or non-obstructive CHD in our study population.

Conclusion

Human plasma PLTP activity was inversely associated with HDL levels and positively related to plasma apoB levels in this Chinese population. Although our findings need to be confirmed in additional studies, they hold the promise that PLTP might be therapeutic target for the treatment of atherosclerosis.

Notes

Declarations

Acknowledgements

This work was supported by grant NIH HL69817, and National Basic Research Program of China (2006CB503803 & 2005CB523302), National High-tech Research and Development Program of China(2006AA02A406), and Outstanding Youth Grant from National Natural Science Fundation of China (30725036).

Authors’ Affiliations

(1)
Institute of Cardiology, Zhongshan Hospital, Fudan University
(2)
Division of Cardiovascular Medicine, SUNY Downstate Medical Center
(3)
Department of Cell Biology, SUNY Downstate Medical Center

References

  1. Schlitt A, Bickel C, Thumma P, Blankenberg S, Rupprecht HJ, Meyer J, Jiang XC: High plasma phospholipid transfer protein levels as a risk factor for coronary artery disease. Arterioscler Thromb Vasc Biol. 2003, 23: 1857-1862. 10.1161/01.ATV.0000094433.98445.7F.View ArticleGoogle Scholar
  2. Tahvanainen E, Jauhiainen M, Funke H, Vartiainen E, Sundvall J, Ehnholm C: Serum phospholipid transfer protein activity and genetic variation of the PLTP gene. Atherosclerosis. 1999, 146: 107-115. 10.1016/S0021-9150(99)00140-9.View ArticleGoogle Scholar
  3. Dullaart RP, Sluiter WJ, Dikkeschei LD, Hoogenberg K, Van Tol A: Effect of adiposity on plasma lipid transfer protein activities: a possible link between insulin resistance and high density lipoprotein metabolism. Eur J Clin Invest. 1994, 24: 188-194. 10.1111/j.1365-2362.1994.tb00987.x.View ArticleGoogle Scholar
  4. Riemens SC, van Tol A, Sluiter WJ, Dullaart RP: Plasma phospholipid transfer protein activity is related to insulin resistance: impaired acute lowering by insulin in obese Type II diabetic patients. Diabetologia. 1998, 41: 929-934. 10.1007/s001250051009.View ArticleGoogle Scholar
  5. Colhoun HM, Scheek LM, Rubens MB, Van Gent T, Underwood SR, Fuller JH, Van Tol A: Lipid transfer protein activities in type 1 diabetic patients without renal failure and nondiabetic control subjects and their association with coronary artery calcification. Diabetes. 2001, 50: 652-659. 10.2337/diabetes.50.3.652.View ArticleGoogle Scholar
  6. Tan KC, Shiu SW, Wong Y, Tam S: Plasma phospholipid transfer protein activity and subclinical inflammation in type 2 diabetes mellitus. Atherosclerosis. 2005, 178: 365-370. 10.1016/j.atherosclerosis.2004.09.005.View ArticleGoogle Scholar
  7. Murdoch SJ, Carr MC, Hokanson JE, Brunzell JD, Albers JJ: PLTP activity in premenopausal women. Relationship with lipoprotein lipase, HDL, LDL, body fat, and insulin resistance. J Lipid Res. 2000, 41: 237-244.Google Scholar
  8. Cheung MC, Knopp RH, Retzlaff B, Kennedy H, Wolfbauer G, Albers JJ: Association of plasma phospholipid transfer protein activity with IDL and buoyant LDL: impact of gender and adiposity. Biochim Biophys Acta. 2002, 1587: 53-59.View ArticleGoogle Scholar
  9. Huuskonen J, Ekstrom M, Tahvanainen E, Vainio A, Metso J, Pussinen P, Ehnholm C, Olkkonen VM, Jauhiainen M: Quantification of human plasma phospholipid transfer protein (PLTP): relationship between PLTP mass and phospholipid transfer activity. Atherosclerosis. 2000, 151: 451-461. 10.1016/S0021-9150(99)00429-3.View ArticleGoogle Scholar
  10. Bosse Y, Bouchard L, Despres JP, Bouchard C, Perusse L, Vohl MC: Haplotypes in the phospholipid transfer protein gene are associated with obesity-related phenotypes: the Quebec Family Study. Int J Obes (Lond). 2005, 29: 1338-1345. 10.1038/sj.ijo.0803010.View ArticleGoogle Scholar
  11. Aouizerat BE, Engler MB, Natanzon Y, Kulkarni M, Song J, Eng C, Huuskonen J, Rivera C, Poon A, Bensley M, Sehnert A, Zellner C, Malloy M, Kane J, Pullinger CR: Genetic variation of PLTP modulates lipoprotein profiles in hypoalphalipoproteinemia. J Lipid Res. 2006, 47: 787-793. 10.1194/jlr.M500476-JLR200.View ArticleGoogle Scholar
  12. Engler MB, Pullinger CR, Malloy MJ, Natanzon Y, Kulkarni MV, Song J, Eng C, Huuskonen J, Rivera C, Poon A, Bensley M, Sehnert A, Zellner C, Kane J, Aouizerat BE: Genetic variation in phospholipid transfer protein modulates lipoprotein profiles in hyperalphalipoproteinemia. Metabolism. 2008, 57: 1719-1724. 10.1016/j.metabol.2008.07.031.View ArticleGoogle Scholar
  13. Tall AR, Krumholz S, Olivecrona T, Deckelbaum RJ: Plasma phospholipid transfer protein enhances transfer and exchange of phospholipids between very low density lipoproteins and high density lipoproteins during lipolysis. J Lipid Res. 1985, 26: 842-851.Google Scholar
  14. Jauhiainen M, Metso J, Pahlman R, Blomqvist S, van Tol A, Ehnholm C: Human plasma phospholipid transfer protein causes high density lipoprotein conversion. J Biol Chem. 1993, 268: 4032-4036.Google Scholar
  15. van Haperen R, van Tol A, Vermeulen P, Jauhiainen M, van Gent T, van den Berg P, Ehnholm S, Grosveld F, Kamp van der A, de Crom R: Human plasma phospholipid transfer protein increases the antiatherogenic potential of high density lipoproteins in transgenic mice. Arterioscler Thromb Vasc Biol. 2000, 20: 1082-1088.View ArticleGoogle Scholar
  16. Foger B, Santamarina-Fojo S, Shamburek RD, Parrot CL, Talley GD, Brewer HB: Plasma phospholipid transfer protein. Adenovirus-mediated overexpression in mice leads to decreased plasma high density lipoprotein (HDL) and enhanced hepatic uptake of phospholipids and cholesteryl esters from HDL. J Biol Chem. 1997, 272: 27393-27400. 10.1074/jbc.272.43.27393.View ArticleGoogle Scholar
  17. van Haperen R, Samyn H, van Gent T, Zonneveld AJ, Moerland M, Grosveld F, Jansen H, Dallinga-Thie GM, van Tol A, de Crom R: Novel roles of hepatic lipase and phospholipid transfer protein in VLDL as well as HDL metabolism. Biochim Biophys Acta. 2009, 1791: 1031-1036.View ArticleGoogle Scholar
  18. van Haperen R, van Tol A, van Gent T, Scheek L, Visser P, Kamp van der A, Grosveld F, de Crom R: Increased risk of atherosclerosis by elevated plasma levels of phospholipid transfer protein. J Biol Chem. 2002, 277: 48938-48943. 10.1074/jbc.M209128200.View ArticleGoogle Scholar
  19. Jiang XC, Bruce C, Mar J, Lin M, Ji Y, Francone OL, Tall AR: Targeted mutation of plasma phospholipid transfer protein gene markedly reduces high-density lipoprotein levels. J Clin Invest. 1999, 103: 907-914. 10.1172/JCI5578.View ArticleGoogle Scholar
  20. Qin S, Kawano K, Bruce C, Lin M, Bisgaier C, Tall AR, Jiang X: Phospholipid transfer protein gene knock-out mice have low high density lipoprotein levels, due to hypercatabolism, and accumulate apoA-IV-rich lamellar lipoproteins. J Lipid Res. 2000, 41: 269-276.Google Scholar
  21. Yan D, Navab M, Bruce C, Fogelman AM, Jiang XC: PLTP deficiency improves the anti-inflammatory properties of HDL and reduces the ability of LDL to induce monocyte chemotactic activity. J Lipid Res. 2004, 45: 1852-1858. 10.1194/jlr.M400053-JLR200.View ArticleGoogle Scholar
  22. Lusa S, Jauhiainen M, Metso J, Somerharju P, Ehnholm C: The mechanism of human plasma phospholipid transfer protein-induced enlargement of high-density lipoprotein particles: evidence for particle fusion. Biochem J. 1996, 313 (Pt 1): 275-282.View ArticleGoogle Scholar
  23. Rye KA, Jauhiainen M, Barter PJ, Ehnholm C: Triglyceride-enrichment of high density lipoproteins enhances their remodelling by phospholipid transfer protein. J Lipid Res. 1998, 39: 613-622.Google Scholar
  24. Masson D, Jiang XC, Lagrost L, Tall AR: The role of plasma lipid transfer proteins in lipoprotein metabolism and atherogenesis. J Lipid Res. 2009, 50 (Suppl): S201-206. 10.1194/jlr.R800061-JLR200.Google Scholar
  25. Tollefson JH, Ravnik S, Albers JJ: Isolation and characterization of a phospholipid transfer protein (LTP-II) from human plasma. J Lipid Res. 1988, 29: 1593-1602.Google Scholar
  26. Kawano K, Qin SC, Lin M, Tall AR, Jiang XC: Cholesteryl ester transfer protein and phospholipid transfer protein have nonoverlapping functions in vivo. J Biol Chem. 2000, 275: 29477-29481. 10.1074/jbc.M003523200.View ArticleGoogle Scholar
  27. Schlitt A, Liu J, Yan D, Mondragon-Escorpizo M, Norin AJ, Jiang XC: Anti-inflammatory effects of phospholipid transfer protein (PLTP) deficiency in mice. Biochim Biophys Acta. 2005, 1733: 187-191.View ArticleGoogle Scholar
  28. Shelly L, Royer L, Sand T, Jensen H, Luo Y: Phospholipid transfer protein deficiency ameliorates diet-induced hypercholesterolemia and inflammation in mice. J Lipid Res. 2008, 49: 773-781. 10.1194/jlr.M700336-JLR200.View ArticleGoogle Scholar
  29. Jiang XC, Tall AR, Qin S, Lin M, Schneider M, Lalanne F, Deckert V, Desrumaux C, Athias A, Witztum JL, Lagrost L: Phospholipid transfer protein deficiency protects circulating lipoproteins from oxidation due to the enhanced accumulation of vitamin E. J Biol Chem. 2002, 277: 31850-31856. 10.1074/jbc.M205077200.View ArticleGoogle Scholar
  30. Yang XP, Yan D, Qiao C, Liu RJ, Chen JG, Li J, Schneider M, Lagrost L, Xiao X, Jiang XC: Increased atherosclerotic lesions in apoE mice with plasma phospholipid transfer protein overexpression. Arterioscler Thromb Vasc Biol. 2003, 23: 1601-1607. 10.1161/01.ATV.0000085841.55248.13.View ArticleGoogle Scholar
  31. Oram JF, Wolfbauer G, Vaughan AM, Tang C, Albers JJ: Phospholipid transfer protein interacts with and stabilizes ATP-binding cassette transporter A1 and enhances cholesterol efflux from cells. J Biol Chem. 2003, 278: 52379-52385. 10.1074/jbc.M310695200.View ArticleGoogle Scholar
  32. Lee-Rueckert M, Vikstedt R, Metso J, Ehnholm C, Kovanen PT, Jauhiainen M: Absence of endogenous phospholipid transfer protein impairs ABCA1-dependent efflux of cholesterol from macrophage foam cells. J Lipid Res. 2006, 47: 1725-1732. 10.1194/jlr.M600051-JLR200.View ArticleGoogle Scholar
  33. Cavusoglu E, Marmur JD, Chhabra S, Chopra V, Eng C, Jiang XC: Relation of baseline plasma phospholipid transfer protein (PLTP) activity to left ventricular systolic dysfunction in patients referred for coronary angiography. Atherosclerosis. 2009, 207: 261-265. 10.1016/j.atherosclerosis.2009.04.011.View ArticleGoogle Scholar
  34. de Vries R, Dallinga-Thie GM, Smit AJ, Wolffenbuttel BH, van Tol A, Dullaart RP: Elevated plasma phospholipid transfer protein activity is a determinant of carotid intima-media thickness in type 2 diabetes mellitus. Diabetologia. 2006, 49: 398-404. 10.1007/s00125-005-0088-0.View ArticleGoogle Scholar
  35. Jiang XC, Qin S, Qiao C, Kawano K, Lin M, Skold A, Xiao X, Tall AR: Apolipoprotein B secretion and atherosclerosis are decreased in mice with phospholipid-transfer protein deficiency. Nat Med. 2001, 7: 847-852. 10.1038/89977.View ArticleGoogle Scholar
  36. Lie J, de Crom R, van Gent T, van Haperen R, Scheek L, Lankhuizen I, van Tol A: Elevation of plasma phospholipid transfer protein in transgenic mice increases VLDL secretion. J Lipid Res. 2002, 43: 1875-1880. 10.1194/jlr.M200166-JLR200.View ArticleGoogle Scholar

Copyright

© Chen et al; licensee BioMed Central Ltd. 2009

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Advertisement