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猪瞬时受体电位通道1促进脂肪生成和脂质沉积。

Porcine transient receptor potential channel 1 promotes adipogenesis and lipid deposition.

作者信息

Fu Yu, Hao Xin, Nie Jingru, Shang Peng, Dong Xinxing, Zhang Bo, Yan Dawei, Zhang Hao

机构信息

Frontiers Science Center for Molecular Design Breeding (MOE), China Agricultural University, Beijing, China; State Key Laboratory of Animal Biotech Breeding, China Agricultural University, Beijing, China.

State Key Laboratory of Animal Biotech Breeding, China Agricultural University, Beijing, China.

出版信息

J Lipid Res. 2025 Jan;66(1):100718. doi: 10.1016/j.jlr.2024.100718. Epub 2024 Dec 3.

Abstract

Adipose tissue, an important organ involved in energy metabolism and endocrine, is closely related to animal meat quality and human health. Transient receptor potential channel 1 (TRPC1), an ion transporter, is adipocytes' major Ca entry channel. However, its function in fat deposition is poorly understood, particularly in pigs, which are both an ideal model for human obesity research and a primary meat source for human diets. In the present investigation, our findings demonstrate a prominent expression of TRPC1 within the adipose tissue of pigs with a strong fat deposition ability. Functional analysis showed that TRPC1 promotes primary preadipocyte proliferation and adipogenic differentiation. In vivo, transgenic mice expressing porcine TRPC1 exhibited aggravated high-fat diet-induced obesity, hepatic steatosis, and insulin resistance. Moreover, TRPC1 may facilitate adipogenesis via activating phosphatidylinositol 3 kinase/AKT and β-catenin signaling pathways. Our research underscores the pivotal role of porcine TRPC1 as a positive regulator in adipogenesis and lipid accumulation processes, providing a potential target for improving animal meat quality and treating obesity-related diseases in humans.

摘要

脂肪组织是参与能量代谢和内分泌的重要器官,与动物肉质和人类健康密切相关。瞬时受体电位通道1(TRPC1)作为一种离子转运体,是脂肪细胞主要的钙离子内流通道。然而,其在脂肪沉积中的功能尚不清楚,尤其是在猪身上,猪既是人类肥胖研究的理想模型,也是人类饮食的主要肉类来源。在本研究中,我们的发现表明,TRPC1在具有较强脂肪沉积能力的猪的脂肪组织中显著表达。功能分析表明,TRPC1可促进原代前脂肪细胞增殖和脂肪生成分化。在体内,表达猪TRPC1的转基因小鼠表现出高脂饮食诱导的肥胖、肝脂肪变性和胰岛素抵抗加重。此外,TRPC1可能通过激活磷脂酰肌醇3激酶/AKT和β-连环蛋白信号通路促进脂肪生成。我们的研究强调了猪TRPC1作为脂肪生成和脂质积累过程中的正调控因子的关键作用,为改善动物肉质和治疗人类肥胖相关疾病提供了潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a3/11741951/9d52d248284a/ga1.jpg

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