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代际饮食诱导的肥胖重塑雌性小鼠网膜脂肪蛋白组。

Generational Diet-Induced Obesity Remodels the Omental Adipose Proteome in Female Mice.

机构信息

Department of Chemistry, University of Kansas, Lawrence, KS 66045, USA.

Ralph N. Adams Institute for Bioanalytical Chemistry, University of Kansas, Lawrence, KS 66047, USA.

出版信息

Nutrients. 2024 Sep 13;16(18):3086. doi: 10.3390/nu16183086.

Abstract

Obesity, a complex condition that involves genetic, environmental, and behavioral factors, is a non-infectious pandemic that affects over 650 million adults worldwide with a rapidly growing prevalence. A major contributor is the consumption of high-fat diets, an increasingly common feature of modern diets. Maternal obesity results in an increased risk of offspring developing obesity and related health problems; however, the impact of maternal diet on the adipose tissue composition of offspring has not been evaluated. Here, we designed a generational diet-induced obesity study in female C57BL/6 mice that included maternal cohorts and their female offspring fed either a control diet (10% fat) or a high-fat diet (45% fat) and examined the visceral adipose proteome. Solubilizing proteins from adipose tissue is challenging due to the need for high concentrations of detergents; however, the use of a detergent-compatible sample preparation strategy based on suspension trapping (S-Trap) enabled label-free quantitative bottom-up analysis of the adipose proteome. We identified differentially expressed proteins related to lipid metabolism, inflammatory disease, immune response, and cancer, providing valuable molecular-level insight into how maternal obesity impacts the health of offspring. Data are available via ProteomeXchange with the identifier PXD042092.

摘要

肥胖是一种涉及遗传、环境和行为因素的复杂病症,是一种非传染性的大流行病,影响着全球超过 6.5 亿成年人,且其发病率还在迅速增长。导致肥胖的一个主要因素是高脂肪饮食的摄入,这是现代饮食越来越普遍的一个特征。母体肥胖会增加后代肥胖和相关健康问题的风险;然而,母体饮食对后代脂肪组织组成的影响尚未得到评估。在这里,我们在雌性 C57BL/6 小鼠中设计了一项代际饮食诱导肥胖研究,包括母体队列及其喂养对照饮食(10%脂肪)或高脂肪饮食(45%脂肪)的雌性后代,并检测了内脏脂肪蛋白质组。由于需要高浓度的去污剂,因此从脂肪组织中溶解蛋白质具有挑战性;然而,使用基于悬浮捕获(S-Trap)的去污剂兼容的样品制备策略,实现了脂肪蛋白质组的无标记定量的自上而下分析。我们鉴定了与脂质代谢、炎症性疾病、免疫反应和癌症相关的差异表达蛋白,为母体肥胖如何影响后代健康提供了有价值的分子水平见解。数据可通过 ProteomeXchange 获取,标识符为 PXD042092。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11435095/ecc916d82775/nutrients-16-03086-g005.jpg

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