Chicken GLUT4 function via enhancing mitochondrial oxidative phosphorylation and inhibiting ribosome pathway in skeletal muscle satellite cells

IF 3.8 1区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Lin Zhang , Pengna Luo , Huihong Li, Yuxian Pan, Huaiyong Zhang, Xuemeng Si, Wen Chen, Yanqun Huang
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引用次数: 0

Abstract

Glucose Transporter 4 (GLUT4) is a crucial protein facilitating glucose uptake and metabolism across cell membranes in mammals. However, information on GLUT4 in birds has historically been limited. In this study, we investigated the dynamic expression profile of chicken GLUT4 using real-time quantitative PCR (RT-qPCR) and examined its potential effects and mechanisms via GLUT4 overexpression and RNA sequencing (RNA-seq) in chicken primary skeletal muscle satellite cells (CP-SMSCs). Our results demonstrated that chicken GLUT4 is differentially expressed across tissues, with predominant expression in skeletal muscles, and across developmental stages of CP-SMSCs, with notable upregulation during the phases of cell proliferation and early differentiation. Notably, 0.1 μM insulin for 60 min significantly elevated the expression of GLUT4 in CP-SMSCs (P < 0.05). GLUT4 overexpression in CP-SMSCs promoted cell proliferation, as evidenced by Cell Counting Kit-8 (CCK-8) (P < 0.05) and 5-Ethynyl-2′-Deoxyuridine (EDU) assays (P < 0.05), and enhanced glucose consumption following 0.1 μM insulin treatment (P < 0.05). However, it inhibited glucose consumption 12 h after the addition of 5 g/L glucose (P < 0.05). After overexpressing GLUT4, we identified 302 differentially expressed genes (DEGs) in CP-SMSCs, with 134 upregulated and 168 downregulated. These DEGs are primarily enriched in pathways such as oxidative phosphorylation, ribosome, cardiac muscle contraction, ATP metabolic processes, and mitochondrial protein complexes. Specifically, in the enriched oxidative phosphorylation pathway, the upregulated DEGs (12) encode mitochondrial proteins, while the downregulated DEGs (6) are nuclear genome-derived. The ribosomal pathway is predominantly inhibited, accompanying with the downregulation of the translocase of outer mitochondrial membrane 7 (TOMM7)/translocase of inner mitochondrial membrane 8 (TIMM8A) complex responsible for mitochondrial protein transport, and a reduction in 28S (LOC121106978) and 18S (LOC112533601) ribosomal rRNAs. In conclusion, chicken GLUT4 is dynamically modulated during development and acts as an insulin responder that significantly regulates cellular glucose uptake and cell proliferation. This regulation occurs mainly through enhancing the mitochondrial oxidative phosphorylation and inhibiting ribosomal pathway.
通过增强骨骼肌卫星细胞线粒体氧化磷酸化和抑制核糖体途径来发挥鸡 GLUT4 的功能。
葡萄糖转运体 4(GLUT4)是哺乳动物体内促进葡萄糖跨细胞膜摄取和新陈代谢的重要蛋白质。然而,有关鸟类 GLUT4 的信息一直很有限。在本研究中,我们利用实时定量 PCR(RT-qPCR)技术研究了鸡 GLUT4 的动态表达谱,并通过鸡原代骨骼肌卫星细胞(CP-SMSCs)中 GLUT4 的过表达和 RNA 测序(RNA-seq)研究了其潜在的作用和机制。我们的研究结果表明,鸡 GLUT4 在不同组织和 CP-SMSCs 不同发育阶段均有不同表达,其中在细胞增殖和早期分化阶段上调明显。值得注意的是,0.1 μM 胰岛素作用 60 分钟可显著提高 CP-SMSCs 中 GLUT4 的表达(P < 0.05)。细胞计数试剂盒-8(CCK-8)(P<0.05)和 5-乙炔基-2'-脱氧尿苷(EDU)检测(P<0.05)表明,CP-SMSCs 中 GLUT4 的过表达促进了细胞增殖,并在 0.1 μM 胰岛素处理后增强了葡萄糖消耗(P<0.05)。然而,在加入 5 g/L 葡萄糖 12 小时后,它抑制了葡萄糖消耗(P < 0.05)。过表达 GLUT4 后,我们在 CP-SMSCs 中发现了 302 个差异表达基因(DEGs),其中 134 个上调,168 个下调。这些 DEGs 主要富集在氧化磷酸化、核糖体、心肌收缩、ATP 代谢过程和线粒体蛋白复合物等通路中。具体来说,在富集的氧化磷酸化途径中,上调的 DEGs(12 个)编码线粒体蛋白,而下调的 DEGs(6 个)来自核基因组。核糖体途径主要受到抑制,负责线粒体蛋白质转运的线粒体外膜转运酶 7 (TOMM7)/ 线粒体内膜转运酶 8 (TIMM8A) 复合物下调,28S(LOC121106978)和 18S (LOC112533601)核糖体 rRNA 减少。总之,鸡 GLUT4 在发育过程中受到动态调控,并作为胰岛素反应器显著调节细胞的葡萄糖摄取和细胞增殖。这种调节主要通过增强线粒体氧化磷酸化和抑制核糖体途径来实现。
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来源期刊
Poultry Science
Poultry Science 农林科学-奶制品与动物科学
CiteScore
7.60
自引率
15.90%
发文量
0
审稿时长
94 days
期刊介绍: First self-published in 1921, Poultry Science is an internationally renowned monthly journal, known as the authoritative source for a broad range of poultry information and high-caliber research. The journal plays a pivotal role in the dissemination of preeminent poultry-related knowledge across all disciplines. As of January 2020, Poultry Science will become an Open Access journal with no subscription charges, meaning authors who publish here can make their research immediately, permanently, and freely accessible worldwide while retaining copyright to their work. Papers submitted for publication after October 1, 2019 will be published as Open Access papers. An international journal, Poultry Science publishes original papers, research notes, symposium papers, and reviews of basic science as applied to poultry. This authoritative source of poultry information is consistently ranked by ISI Impact Factor as one of the top 10 agriculture, dairy and animal science journals to deliver high-caliber research. Currently it is the highest-ranked (by Impact Factor and Eigenfactor) journal dedicated to publishing poultry research. Subject areas include breeding, genetics, education, production, management, environment, health, behavior, welfare, immunology, molecular biology, metabolism, nutrition, physiology, reproduction, processing, and products.
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