FABP1 通过调节大黄鱼肝细胞中 SREBP1 的加工过程诱导脂肪生成

IF 4.4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Fan Chen, Tingting Hao, Qiang Chen, Yuning Sun, Yanan Shen, Zengqi Zhao, Jianlong Du, Yueru Li, Kangsen Mai, Qinghui Ai
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引用次数: 0

摘要

脂肪酸结合蛋白 1(FABP1)在调节肝脏脂肪酸代谢方面发挥着重要作用,是非酒精性脂肪肝等疾病的潜在治疗靶点。然而,其潜在机制尚未明确。利用互补实验模型,我们发现当暴露于脂肪酸,尤其是饱和脂肪酸(SFA)时,肝细胞中的 FABP1 诱导是脂肪生成的主要介质。在喂养试验中,棕榈油导致大黄鱼(Larimichthys crocea)肝脏中脂质过度积累,同时显著诱导 FABP1。在培养细胞中,棕榈酸(PA)(一种 SFA)可诱导 fabp1 的表达并增加甘油三酯(TG)含量。敲除 FABP1 可通过减轻脂肪生成来抑制 PA 诱导的 TG 累积。而过表达 FABP1 则显示出相反的结果。此外,FABP1 的失活导致胰岛素诱导基因 1(INSIG1)表达的诱导,INSIG1 通过下调核定位的 SREBP1 来减弱固醇调节元件结合蛋白 1(SREBP1)的处理。这些结果揭示了 FABP1 在应对 PA 时的一种之前未被认识到的功能,为靶向 FABP1 治疗 SFA 引起的非酒精性脂肪肝提供了更多证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

FABP1 induces lipogenesis by regulating the processing of SREBP1 in hepatocytes of large yellow croaker (Larimichthys crocea)

FABP1 induces lipogenesis by regulating the processing of SREBP1 in hepatocytes of large yellow croaker (Larimichthys crocea)

Fatty acid-binding protein 1 (FABP1) plays an important role in regulating fatty acid metabolism in liver, which is a potential therapeutic target for diseases such as non-alcoholic fatty liver disease (NAFLD). However, the underlying mechanisms are not well defined. Using complementary experimental models, we discovered FABP1 induction in hepatocytes as a primary mediator of lipogenesis when exposed to fatty acids, especially saturated fatty acids (SFAs). In the feeding trial, palm oil led to excess lipid accumulation in the liver of large yellow croaker (Larimichthys crocea), accompanied by significant induction of FABP1. In cultured cells, palmitic acid (PA), a kind of SFA, triggered the fabp1 expression and increased triglyceride (TG) contents. Knockdown of FABP1 dampened PA-induced TG accumulation through mitigated lipogenesis. The overexpression of FABP1 showed the opposite result. Furthermore, the inactivation of FABP1 led to induction in insulin-induced gene 1 (INSIG1) expression, which attenuated the processing of sterol regulatory element-binding protein 1 (SREBP1) by down-regulating the nuclear-localized SREBP1. These results revealed a previously unrecognized function of FABP1 in response to PA, providing additional evidence for targeting FABP1 in the treatment of NAFLD caused by SFA.

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来源期刊
FASEB Journal
FASEB Journal 生物-生化与分子生物学
CiteScore
9.20
自引率
2.10%
发文量
6243
审稿时长
3 months
期刊介绍: The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.
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