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家族性高胆固醇血症动物模型WHHL兔肝脏和肾上腺中低密度脂蛋白受体的缺乏。

Deficiency of low density lipoprotein receptors in liver and adrenal gland of the WHHL rabbit, an animal model of familial hypercholesterolemia.

作者信息

Kita T, Brown M S, Watanabe Y, Goldstein J L

出版信息

Proc Natl Acad Sci U S A. 1981 Apr;78(4):2268-72. doi: 10.1073/pnas.78.4.2268.

Abstract

The WHHL (Watanabe heritable hyperlipidemic) rabbit has been proposed as an animal model for human familial hypercholesterolemia. Homozygous WHHL rabbits have marked increases in the plasma level of low density lipoprotein (LDL), removal of LDL from their plasma is delayed, and LDL receptors are absent from their cultured fibroblasts [Tanzawa, K., Shimada, Y., Kuroda, M., Tsujita, Y., Arai, M. & Watanabe, Y. (1980) FEBS Lett. 118, 81--84]. We here report that membranes from the liver and adrenal gland of WHHL rabbits lack high-affinity LDL receptors. In normal rabbit membranes, binding of LDL to this receptor required calcium and is inhibited by EDTA. The LDL receptor binds rabbit 125I-labeled beta-migrating very low density lipoprotein (beta-VLDL), which contains apoproteins B and E, as well as rabbit 125I-labeled LDL, which contains only apoprotein B. It does not bind high density lipoprotein or methyl-LDL. All of these properties are identical with those of the LDL receptor of cultured fibroblasts. We conclude that a deficiency of hepatic and adrenal LDL receptors contributes to the hypercholesterolemia of the WHHL rabbits.

摘要

渡边遗传性高脂血症(WHHL)兔已被提议作为人类家族性高胆固醇血症的动物模型。纯合子WHHL兔的低密度脂蛋白(LDL)血浆水平显著升高,LDL从其血浆中的清除延迟,且其培养的成纤维细胞中不存在LDL受体[Tanzawa, K., Shimada, Y., Kuroda, M., Tsujita, Y., Arai, M. & Watanabe, Y. (1980) FEBS Lett. 118, 81--84]。我们在此报告,WHHL兔肝脏和肾上腺的膜缺乏高亲和力LDL受体。在正常兔膜中,LDL与该受体的结合需要钙,并受到EDTA的抑制。LDL受体结合含有载脂蛋白B和E的兔125I标记的β迁移极低密度脂蛋白(β-VLDL),以及仅含有载脂蛋白B的兔125I标记的LDL。它不结合高密度脂蛋白或甲基化LDL。所有这些特性与培养的成纤维细胞的LDL受体相同。我们得出结论,肝脏和肾上腺LDL受体的缺乏导致了WHHL兔的高胆固醇血症。

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