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膳食胆碱通过 DNA 甲基化调控 UPRer 减轻高脂肪饮食引起的乳糜微粒组装障碍。

Dietary Choline Mitigates High-Fat Diet-Impaired Chylomicrons Assembly via UPRer Modulated by DNA Methylation.

机构信息

Key Laboratory of Freshwater Animal Breeding, Ministry of Agriculture, Fishery College, Huazhong Agricultural University, Wuhan 430070, China.

Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China.

出版信息

Cells. 2022 Nov 30;11(23):3848. doi: 10.3390/cells11233848.

Abstract

High-fat diets (HFD) lead to impairment of chylomicrons (CMs) assembly and adversely influence intestinal lipid homeostasis. However, the mechanisms of HFD impairing CMs assembly have yet to be fully understood. Additionally, although choline, as a lipid-lowering agent, has been widely used and its deficiency has been closely linked to non-alcoholic steatohepatitis (NASH), the contribution of choline by functioning as a methyl donor in alleviating HFD-induced intestinal lipid deposition is unknown. Thus, this study was conducted to determine the mechanism of HFD impairing CMs assembly and also tested the effect of choline acting as a methyl donor in this process. To this end, in this study, four diets (control, HFD, choline and HFD + choline diet) were fed to yellow catfish for 10 weeks in vivo and their intestinal epithelial cells were isolated and incubated for 36 h in fatty acids (FA) with or without choline solution combining si- transfection in vitro. The key findings from this study as follows: (1) HFD caused impairment of CMs assembly main by unfolded protein response (UPRer). HFD activated and then induced UPRer, which led to endoplasmic reticulum dysfunction and further impaired CMs assembly via protein-protein interactions between Perk and Apob48. (2) Choline inhibited the transcriptional expression level of via activating the - CpG methylation site, which initiated the subsequent ameliorating effect on HFD-impaired CMs assembly and intestinal lipid dysfunction. These results provide a new insight into direct crosstalk between UPRer and CMs assembly, and also emphasize the critical contribution of choline acting as a methyl donor and shed new light on choline-deficient diet-induced NASH.

摘要

高脂肪饮食(HFD)导致乳糜微粒(CMs)组装受损,并对肠道脂质稳态产生不利影响。然而,HFD 损害 CMs 组装的机制尚未完全阐明。此外,尽管胆碱作为降脂剂被广泛应用,并且其缺乏与非酒精性脂肪性肝炎(NASH)密切相关,但胆碱作为甲基供体在缓解 HFD 诱导的肠道脂质沉积中的作用尚不清楚。因此,本研究旨在确定 HFD 损害 CMs 组装的机制,并测试胆碱作为甲基供体在这一过程中的作用。为此,本研究在体内用四种饮食(对照、HFD、胆碱和 HFD+胆碱饮食)喂养黄颡鱼 10 周,然后分离其肠道上皮细胞,并在体外与或不与胆碱溶液结合 si 转染孵育 36 小时脂肪酸(FA)。本研究的主要发现如下:(1)HFD 通过未折叠蛋白反应(UPRer)导致 CMs 组装受损。HFD 激活 PERK,然后诱导 UPRer,导致内质网功能障碍,并通过 PERK 和 Apob48 之间的蛋白-蛋白相互作用进一步损害 CMs 组装。(2)胆碱通过激活- CpG 甲基化位点抑制 的转录表达水平,从而对 HFD 损害的 CMs 组装和肠道脂质功能障碍产生后续的改善作用。这些结果为 UPRer 和 CMs 组装之间的直接相互作用提供了新的见解,并强调了胆碱作为甲基供体的关键作用,为胆碱缺乏饮食诱导的 NASH 提供了新的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8957/9741040/21fdc463a976/cells-11-03848-g002.jpg

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