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微阵列、抗肥胖与肝脏

Microarrays, antiobesity and the liver.

作者信息

Castro-Chávez Fernando

机构信息

Departamento de Biología Molecular en Medicina, Hospital Civil de Belén, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, México.

出版信息

Ann Hepatol. 2004 Oct-Dec;3(4):137-45.

Abstract

In this review, the microarray technology and especially oligonucleotide arrays are exemplified with a practical example taken from the perilipin-/- mice and using the dChip software, available for non-lucrative purposes. It was found that the liver of perilipin-/- mice was healthy and normal, even under high-fat diet when compared with the results published for the scd1-/- mice, which under high-fat diets had a darker liver, suggestive of hepatic steatosis. Scd1 is required for the biosynthesis of monounsaturated fatty acids and plays a key role in the hepatic synthesis of triglycerides and of very-low-density lipoproteins. Both models of obesity resistance share many similar phenotypic antiobesity features, however, the perilipin-/- mice had a significant downregulation of stearoyl CoA desaturases scd1 and scd2 in its white adipose tissue, but a normal level of both genes inside the liver, even under high-fat diet. Here, different microarray methodologies are discussed, and also some of the most recent discoveries and perspectives regarding the use of microarrays, with an emphasis on obesity gene expression, and a personal remark on my findings of increased expression for hemoglobin transcripts and other hemo related genes (hemo-like), and for leukocyte like (leuko-like) genes inside the white adipose tissue of the perilipin-/- mice. In conclusion, microarrays have much to offer in comparative studies such as those in antiobesity, and also they are methodologies adequate for new astounding molecular discoveries [free full text of this article Online].

摘要

在本综述中,以取自围脂滴蛋白基因敲除(perilipin-/-)小鼠的一个实际例子,并使用可用于非盈利目的的dChip软件,对微阵列技术尤其是寡核苷酸阵列进行了举例说明。研究发现,与已发表的硬脂酰辅酶A去饱和酶1(scd1-/-)小鼠的结果相比,即使在高脂饮食条件下,perilipin-/-小鼠的肝脏也是健康且正常的。scd1-/-小鼠在高脂饮食时肝脏颜色较深,提示有肝脂肪变性。单不饱和脂肪酸的生物合成需要scd1,它在肝脏甘油三酯和极低密度脂蛋白的合成中起关键作用。两种抗肥胖模型都有许多相似的抗肥胖表型特征,然而,perilipin-/-小鼠白色脂肪组织中的硬脂酰辅酶A去饱和酶scd1和scd2显著下调,但其肝脏内这两个基因的水平正常,即使在高脂饮食条件下也是如此。本文讨论了不同的微阵列方法,以及关于微阵列使用的一些最新发现和观点,重点是肥胖基因表达,并对我在perilipin-/-小鼠白色脂肪组织中发现血红蛋白转录本和其他血红素相关基因(类血红素)以及类白细胞基因表达增加的结果发表了个人看法。总之,微阵列在抗肥胖等比较研究中有很大作用,并且它们也是适用于新的惊人分子发现的方法[本文免费全文在线获取] 。

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