Low-density Lipoprotein Regulates Intestinal Stem Cell Homeostasis via PPAR Pathway.

IF 5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ruicheng Shi, Wei Lu, Zhiming Zhao, Bo Wang
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引用次数: 0

Abstract

Epidemiological studies have highlighted a strong association between hyperlipidemia and an increased risk of cancer in the gut. Intestinal stem cells (ISCs) have been demonstrated as the cells of origin for tumorigenesis in the gut. However, the impact of hyperlipidemia on ISC homeostasis remains unclear. Here, we show that hyperlipidemia induced by low-density lipoprotein receptor (Ldlr) deficiency enhances ISC proliferation in vivo. Additionally, LDL treatment impairs organoid survival but increases ISC stemness ex vivo, as evidenced by the formation of poorly differentiated spheroid and higher ISC self-renewal capacity. Mechanistically, LDL treatment activates PPAR pathways, and pharmacological inhibition of PPAR and its downstream targets, including CPT1A and PDK4, mitigates the effect of LDL on ISCs. These findings demonstrate that hyperlipidemia modulates ISC homeostasis, providing new insights into the mechanism linking hyperlipidemia with tumorigenesis in the gut.

低密度脂蛋白通过PPAR通路调控肠道干细胞稳态。
流行病学研究强调了高脂血症与肠道癌症风险增加之间的密切联系。肠干细胞(ISCs)已被证明是肠道肿瘤发生的起源细胞。然而,高脂血症对ISC稳态的影响尚不清楚。本研究表明,低密度脂蛋白受体(Ldlr)缺乏诱导的高脂血症可促进体内ISC的增殖。此外,LDL治疗会损害类器官的存活,但会增加体外ISC的干性,这可以从低分化球体的形成和更高的ISC自我更新能力中得到证明。从机制上讲,LDL处理激活了PPAR通路,药理抑制PPAR及其下游靶点,包括CPT1A和PDK4,减轻了LDL对ISCs的影响。这些发现表明,高脂血症调节ISC稳态,为高脂血症与肠道肿瘤发生的联系机制提供了新的见解。
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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来源期刊
Journal of Lipid Research
Journal of Lipid Research 生物-生化与分子生物学
CiteScore
11.10
自引率
4.60%
发文量
146
审稿时长
41 days
期刊介绍: The Journal of Lipid Research (JLR) publishes original articles and reviews in the broadly defined area of biological lipids. We encourage the submission of manuscripts relating to lipids, including those addressing problems in biochemistry, molecular biology, structural biology, cell biology, genetics, molecular medicine, clinical medicine and metabolism. Major criteria for acceptance of articles are new insights into mechanisms of lipid function and metabolism and/or genes regulating lipid metabolism along with sound primary experimental data. Interpretation of the data is the authors’ responsibility, and speculation should be labeled as such. Manuscripts that provide new ways of purifying, identifying and quantifying lipids are invited for the Methods section of the Journal. JLR encourages contributions from investigators in all countries, but articles must be submitted in clear and concise English.
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