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脂肪细胞来源的外泌体通过 GRP78 调节草鱼原代肝细胞的脂代谢

Regulation of lipid metabolism in grass carp primary hepatocytes by exosomes derived from fatty hepatocytes though GRP78.

机构信息

College of Fisheries, Henan Normal University, No. 46 Jianshe Road, Xinxiang, 453007, China.

出版信息

Fish Physiol Biochem. 2024 Dec;50(6):2287-2299. doi: 10.1007/s10695-024-01384-9. Epub 2024 Aug 2.

DOI:10.1007/s10695-024-01384-9
PMID:39090453
Abstract

Exosomes regulate lipid metabolism by carrying miRNAs, nucleic acids, and proteins, thereby influencing the function of receptor cells. Glucose-regulated protein 78 (GRP78) is also involved in the regulation of lipid metabolism. However, it remains unclear whether exosomes derived from fatty hepatocytes (OA-Exo) regulate lipid metabolism through the enrichment of GRP78. In this study, we observed the expression of GRP78 was significantly increased in fatty hepatocytes (incubating hepatocytes with oleic acid (OA) for 24 h) and OA-Exo (P < 0.05). In addition, OA-Exo (50 μg/mL) and GRP78 protein (1 μg/mL) significant increased the content of triacylglycerol (TG) and total cholesterol (TC), as well as up-regulated the expression of GRP78 and inositol-requiring enzyme-1alpha (IRE1α) protein (P < 0.05). We further used YUM70 (an inhibitor of GRP78) to inhibit endogenous GRP78, and compared with the YUM70 group, OA-Exo reversed the effect of YUM70 and increased the content of TG, TC, and the expression of GRP78 protein in hepatocytes (P < 0.05). Furthermore, the inhibition of the IRE1α pathway with 4μ8C resulted in a significant decrease in TG content compared to the control group (P < 0.05). However, when compared with the 4μ8C group, OA-Exo and GRP78 reversed the effect of 4μ8C and significantly increased TG content (P < 0.05). Taken together, these results indicated that OA-Exo activated IRE1α to promote lipid accumulation in hepatocytes through the enrichment of GRP78. This study provided a new perspective for further exploration of exosomal lipid metabolism in fish.

摘要

外泌体通过携带 miRNA、核酸和蛋白质来调节脂质代谢,从而影响受体细胞的功能。葡萄糖调节蛋白 78(GRP78)也参与脂质代谢的调节。然而,目前尚不清楚来自脂肪性肝细胞的外泌体(OA-Exo)是否通过富集 GRP78 来调节脂质代谢。在本研究中,我们观察到脂肪性肝细胞(用油酸(OA)孵育肝细胞 24 小时)和 OA-Exo 中 GRP78 的表达显著增加(P<0.05)。此外,OA-Exo(50μg/mL)和 GRP78 蛋白(1μg/mL)显著增加了三酰甘油(TG)和总胆固醇(TC)的含量,并上调了 GRP78 和肌醇需求酶 1α(IRE1α)蛋白的表达(P<0.05)。我们进一步使用 YUM70(GRP78 的抑制剂)抑制内源性 GRP78,与 YUM70 组相比,OA-Exo 逆转了 YUM70 的作用,并增加了肝细胞中 TG、TC 和 GRP78 蛋白的含量(P<0.05)。此外,与对照组相比,用 4μ8C 抑制 IRE1α 通路导致 TG 含量显著降低(P<0.05)。然而,与 4μ8C 组相比,OA-Exo 和 GRP78 逆转了 4μ8C 的作用,并显著增加了 TG 含量(P<0.05)。综上所述,这些结果表明,OA-Exo 通过富集 GRP78 激活 IRE1α,促进肝细胞中脂质的积累。本研究为进一步探索鱼类外泌体脂质代谢提供了新的视角。

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本文引用的文献

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Anim Nutr. 2023 Jul 29;15:126-136. doi: 10.1016/j.aninu.2023.07.003. eCollection 2023 Dec.
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Tumor-secreted GRP78 induces M2 polarization of macrophages by promoting lipid catabolism.肿瘤分泌的 GRP78 通过促进脂质分解诱导巨噬细胞 M2 极化。
Cell Signal. 2023 Aug;108:110719. doi: 10.1016/j.cellsig.2023.110719. Epub 2023 May 18.
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The Roles of Exosomal Proteins: Classification, Function, and Applications.
外泌体蛋白的作用:分类、功能及应用。
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S100A10 promotes HCC development and progression via transfer in extracellular vesicles and regulating their protein cargos.S100A10 通过在细胞外囊泡中转移和调节其蛋白 cargo 促进 HCC 的发展和进展。
Gut. 2023 Jul;72(7):1370-1384. doi: 10.1136/gutjnl-2022-327998. Epub 2023 Jan 11.
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Exosomal RBP4 potentiated hepatic lipid accumulation and inflammation in high-fat-diet-fed mice by promoting M1 polarization of Kupffer cells.外泌体 RBP4 通过促进库普弗细胞 M1 极化促进高脂肪饮食喂养小鼠的肝脂质积累和炎症。
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Cell-Derived Vesicles for mRNA Delivery.用于mRNA递送的细胞衍生囊泡
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Gastric Cancer Cell-Derived Exosomal GRP78 Enhances Angiogenesis upon Stimulation of Vascular Endothelial Cells.胃癌细胞衍生的外泌体GRP78在刺激血管内皮细胞时增强血管生成。
Curr Issues Mol Biol. 2022 Dec 6;44(12):6145-6157. doi: 10.3390/cimb44120419.
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Upper gut heat shock proteins HSP70 and GRP78 promote insulin resistance, hyperglycemia, and non-alcoholic steatohepatitis.上消化道热休克蛋白 HSP70 和 GRP78 促进胰岛素抵抗、高血糖和非酒精性脂肪性肝炎。
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