卵磷脂胆固醇酰基转移酶缺陷小鼠中胆固醇酯转移蛋白的表达

Cheng-ai Wu, M. Tsujita, K. Okumura‐Noji, S. Usui, Hajime Kakuuchi, M. Okazaki, S. Yokoyama
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引用次数: 5

摘要

目的:研究卵磷脂-胆固醇酰基转移酶(LCAT)敲除小鼠血浆胆固醇酯转移蛋白(CETP)浓度的变化。方法与结果:lcat基因敲除小鼠与CETP转基因小鼠杂交。后代(n=63)根据LCAT基因型和血浆CETP水平(无CETP、低CETP和高CETP)进行分类。各cetp水平组高密度脂蛋白(HDL)随LCAT的降低而降低。lcat(+/+)和lcat(+/−)小鼠血浆CETP变化范围为0 ~ 30 μ g/mL,而lcat(−/−)小鼠血浆CETP变化范围<10 μ g/mL。lcat(+/+)和lcat(+/−)小鼠的CETP中HDL胆固醇和磷脂降低,HDL甘油三酯和载脂蛋白B升高,而低CETP和高CETP之间HDL无差异。由于缺乏成熟的HDL,在lcat(−/−)小鼠中未检测到CETP对HDL的影响。在lcat(−/−)和lcat(+/+)小鼠中,基因组DNA和CETP mRNA呈相关且相似。血浆CETP与其基因组DNA和mRNA相关,但在lcat(−/−)小鼠中增加的斜率要低得多。血浆CETP在lcat(+/+)小鼠中主要与HDL相关,而在lcat(- /−)小鼠中则是游离的。结论:lcat(−/−)小鼠血浆CETP转录后下调,可能是由于其极低的HDL。
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Cholesteryl Ester Transfer Protein Expressed in Lecithin Cholesterol Acyltransferase–Deficient Mice
Objective—Regulation of plasma cholesteryl ester transfer protein (CETP) concentration was studied in lecithin-cholesterol acyltransferase (LCAT)-knockout mice. Methods and Results—LCAT-knockout mice were cross-bred with CETP transgenic mice. The offspring (n=63) were classified for LCAT genotype and plasma CETP levels (no CETP, low CETP, and high CETP). High density lipoprotein (HDL) decreased as LCAT decreased in each CETP-level group. In the lcat(+/+) and lcat(+/ −) mice, plasma CETP varied from 0 to 30 &mgr;g/mL, whereas it was <10 &mgr;g/mL in the lcat( −/ −) mice. HDL cholesterol and phospholipid decreased and HDL triglyceride and apolipoprotein B increased in CETP in the lcat(+/+) and lcat(+/ −) mice, whereas there was no difference in HDL between low and high CETP. An effect of CETP on HDL was not detected in the lcat( −/ −) mice because of the absence of mature HDL. Genomic DNA and mRNA of CETP were correlated and were similar in the lcat( −/ −) and lcat(+/+) mice. Plasma CETP was correlated with its genomic DNA and mRNA, but the slope of the increase was much lower in the lcat( −/ −) mice. Whereas plasma CETP mostly associates with HDL in the lcat(+/+) mouse, it is found free in the lcat( −/ −) mouse. Conclusions—Plasma CETP is posttranscriptionally downregulated in the lcat( −/ −) mice, presumably by its extremely low HDL.
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