缺乏Stap1全局表达的小鼠不表现高胆固醇血症。

4区 医学 Q4 Medicine BMC Medical Genetics Pub Date : 2020-11-23 DOI:10.1186/s12881-020-01176-x
Babunageswararao Kanuri, Vincent Fong, April Haller, David Y Hui, Shailendra B Patel
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引用次数: 4

摘要

背景:常染色体显性家族性高胆固醇血症(ADH;MIM#143890)是最常见的单基因疾病之一,其特征是循环LDL胆固醇升高。对ADH患者的初步研究发现,ADH与编码信号转导接头家族成员蛋白1 (STAP1;MIM # 604298)。然而,随后的研究结果却相互矛盾。在这项研究中,缺乏Stap1全局表达(Stap1-/-)的小鼠在标准食物和42% kcal西方饮食(WD)下进行了表征。方法:研究小鼠在16周WD方案前后不同代谢参数的变化。研究了生长曲线、体脂、循环脂、葡萄糖稳态参数和肝脏结构进行比较。结果:令人惊讶的是,与Stap1+/+小鼠相比,饲喂16周WD的Stap1-/-小鼠在任何代谢参数上都没有显着差异。此外,hplc分离的脂蛋白组分中的肝脏结构和胆固醇含量也与野生型小鼠相当。结论:这些结果强烈提示STAP1不会改变脂质水平,西方饮食不会加剧STAP1缺陷小鼠的脂质紊乱,并支持它不是ADH患者高脂血症病因的论点。这些结果支持了其他已发表的研究,这些研究也质疑该基因座在人类高胆固醇血症中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Mice lacking global Stap1 expression do not manifest hypercholesterolemia.

Background: Autosomal dominant familial hypercholesterolemia (ADH; MIM#143890) is one of the most common monogenic disorders characterized by elevated circulatory LDL cholesterol. Initial studies in humans with ADH identified a potential relationship with variants of the gene encoding signal transducing adaptor family member protein 1 (STAP1; MIM#604298). However, subsequent studies have been contradictory. In this study, mice lacking global Stap1 expression (Stap1-/-) were characterized under standard chow and a 42% kcal western diet (WD).

Methods: Mice were studied for changes in different metabolic parameters before and after a 16-week WD regime. Growth curves, body fats, circulatory lipids, parameters of glucose homeostasis, and liver architecture were studied for comparisons.

Results: Surprisingly, Stap1-/- mice fed the 16-week WD demonstrated no marked differences in any of the metabolic parameters compared to Stap1+/+ mice. Furthermore, hepatic architecture and cholesterol content in FPLC-isolated lipoprotein fractions also remained comparable to wild-type mice.

Conclusion: These results strongly suggest that STAP1 does not alter lipid levels, that a western diet did not exacerbate a lipid disorder in Stap1 deficient mice and support the contention that it is not causative for hyperlipidemia in ADH patients. These results support other published studies also questioning the role of this locus in human hypercholesterolemia.

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来源期刊
BMC Medical Genetics
BMC Medical Genetics 医学-遗传学
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审稿时长
12 months
期刊介绍: BMC Medical Genetics is an open access journal publishing original peer-reviewed research articles in the effects of genetic variation in individuals, families and among populations in relation to human health and disease. Note: BMC Medical Genetics is now closed. This journal has merged with BMC Medical Genomics, a broad-scope, open access community journal for all medical genetics and genomics research.
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