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载脂蛋白(a)和载脂蛋白B对小鼠主动脉近端脂肪病变发展的相对贡献。

Relative contributions of apolipoprotein(a) and apolipoprotein-B to the development of fatty lesions in the proximal aorta of mice.

作者信息

Mancini F P, Newland D L, Mooser V, Murata J, Marcovina S, Young S G, Hammer R E, Sanan D A, Hobbs H H

机构信息

Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235-9046, USA.

出版信息

Arterioscler Thromb Vasc Biol. 1995 Nov;15(11):1911-6. doi: 10.1161/01.atv.15.11.1911.

DOI:10.1161/01.atv.15.11.1911
PMID:7583571
Abstract

Transgenic mice expressing transgenes for both human apolipoprotein B-100 (h-apoB) and apolipoprotein(a) [apo(a)] were fed a high-fat, atherogenic diet for 14 weeks to examine the effect of lipoprotein(a) [Lp(a)]on the development of aortic fatty lesions. The extent of lesions in the proximal region of the aorta of Lp(a) mice was measured by use of a computer-assisted image analysis of 20 sections per animal and compared with that of nontransgenic mice as well as mice expressing either the apo(a) or h-apoB transgene. The control (n = 23) and apo(a) (n = 22) transgenic mice had very small mean lesions areas (607 versus 128 microns2 per section). The h-apoB-expressing mice (n = 20) had significantly higher mean lesion areas (3288 microns2 per section) than either the control or apo(a) transgenic animals. Coexpression of apo(a) and h-apoB transgenes resulted in only a modest increase in lesion area (4678 microns2 per section, n = 19). Thus, the expression of human apo(a) in C57BL/6/SJL hybrid mice fed an atherogenic diet failed to significantly potentiate the development of aortic fatty lesions in the absence or presence of high levels of h-apoB.

摘要

给同时表达人类载脂蛋白B - 100(h - apoB)和载脂蛋白(a) [apo(a)]转基因的小鼠喂食高脂致动脉粥样化饮食14周,以研究脂蛋白(a) [Lp(a)]对主动脉脂肪病变发展的影响。通过对每只动物的20个切片进行计算机辅助图像分析,测量Lp(a)小鼠主动脉近端区域的病变程度,并与非转基因小鼠以及表达apo(a)或h - apoB转基因的小鼠进行比较。对照(n = 23)和apo(a)(n = 22)转基因小鼠的平均病变面积非常小(每切片分别为607和128平方微米)。表达h - apoB的小鼠(n = 20)的平均病变面积(每切片3288平方微米)显著高于对照或apo(a)转基因动物。apo(a)和h - apoB转基因的共表达仅使病变面积适度增加(每切片4678平方微米,n = 19)。因此,在喂食致动脉粥样化饮食的C57BL/6/SJL杂交小鼠中,无论是否存在高水平的h - apoB,人类apo(a)的表达均未能显著增强主动脉脂肪病变的发展。

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