• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

脂质调节元件在牛脂肪细胞分化和脂代谢中的线粒体生物能学中与 相互作用。

Lipid Regulatory Element Interact with on Mitochondrial Bioenergetics in Bovine Adipocyte Differentiation and Lipometabolism.

机构信息

College of Animal Science, Jilin University, 5333 Xi An Road, Changchun, Jilin 130062, People's Republic of China.

Key Laboratory of Genetics and Breeding, Zhejiang Institute of Freshwater Fisheries, 999 Hangchangqiao South Road, Huzhou, Zhejiang 313000, People's Republic of China.

出版信息

J Agric Food Chem. 2024 Aug 7;72(31):17481-17498. doi: 10.1021/acs.jafc.4c02434. Epub 2024 Jul 29.

DOI:10.1021/acs.jafc.4c02434
PMID:39072486
Abstract

The gene is a critical factor in animal physiological processes and has been shown to affect insulin resistance and fat accumulation in mammals. Nevertheless, little research has been conducted on its precise functions in lipid metabolism and adipogenic differentiation in beef cattle. This study analyzed the expression of and miR-199a-3p during bovine preadipocyte differentiation. The luciferase reporter assay demonstrated that was a direct target of miR-199a-3p. Increased accumulation of lipid droplets and triglyceride levels, altered fatty acid metabolism, and accelerated preadipocyte differentiation were all caused by the upregulation of miR-199a-3p or a reduction in expression. knockdown upregulated the expression of adipocyte-specific genes ( and ) and altered the levels of lipid metabolites (SOPC, l-arginine, and heptadecanoic acid). Multiomics highlights enriched pathways involved in energy metabolism (MAPK, cAMP, and calcium signaling) and shifts in mitochondrial respiration and glycolysis, indicating that plays a regulatory role in lipid metabolism. The findings show that intracellular lipolysis, glycolysis, mitochondrial respiration, fat deposition, and lipid droplet composition are all impacted by miR-199a-3p, which modulates in bovine adipocytes.

摘要

该基因是动物生理过程的关键因素,已被证明会影响哺乳动物的胰岛素抵抗和脂肪积累。然而,关于其在肉牛脂质代谢和脂肪生成分化中的精确功能,研究甚少。本研究分析了在牛前体脂肪细胞分化过程中 和 miR-199a-3p 的表达。荧光素酶报告基因检测表明, 是 miR-199a-3p 的直接靶基因。miR-199a-3p 的上调或 表达的减少,导致脂滴和甘油三酯水平的积累增加、脂肪酸代谢改变和前体脂肪细胞分化加速。 敲低可上调脂肪细胞特异性基因( 和 )的表达,并改变脂质代谢物(SOPC、l-精氨酸和十七烷酸)的水平。多组学突出显示涉及能量代谢(MAPK、cAMP 和钙信号转导)的富集途径以及线粒体呼吸和糖酵解的变化,表明 在脂质代谢中发挥调节作用。研究结果表明,miR-199a-3p 调节 可影响细胞内脂肪分解、糖酵解、线粒体呼吸、脂肪沉积和脂质滴组成,从而调节牛脂肪细胞中的脂质代谢。

相似文献

1
Lipid Regulatory Element Interact with on Mitochondrial Bioenergetics in Bovine Adipocyte Differentiation and Lipometabolism.脂质调节元件在牛脂肪细胞分化和脂代谢中的线粒体生物能学中与 相互作用。
J Agric Food Chem. 2024 Aug 7;72(31):17481-17498. doi: 10.1021/acs.jafc.4c02434. Epub 2024 Jul 29.
2
miR-130b duplex (miR-130b-3p/miR-130b-5p) negatively regulates goat intramuscular preadipocyte lipid droplets accumulation by inhibiting Krüppel-like factor 3 expression.miR-130b 双体(miR-130b-3p/miR-130b-5p)通过抑制 Krüppel 样因子 3 的表达来负调控山羊肌内前体脂肪细胞的脂滴积累。
J Anim Sci. 2023 Jan 3;101. doi: 10.1093/jas/skad184.
3
miR-199a-3p regulates brown adipocyte differentiation through mTOR signaling pathway.miR-199a-3p 通过 mTOR 信号通路调节棕色脂肪细胞分化。
Mol Cell Endocrinol. 2018 Nov 15;476:155-164. doi: 10.1016/j.mce.2018.05.005. Epub 2018 Jun 28.
4
miR-199a-3p affects adipocytes differentiation and fatty acid composition through targeting SCD.微小RNA-199a-3p通过靶向硬脂酰辅酶A去饱和酶影响脂肪细胞分化和脂肪酸组成。
Biochem Biophys Res Commun. 2017 Oct 7;492(1):82-88. doi: 10.1016/j.bbrc.2017.08.030. Epub 2017 Aug 10.
5
Bta-miR-130a/b regulates preadipocyte differentiation by targeting PPARG and CYP2U1 in beef cattle.Bta-miR-130a/b 通过靶向 PPARG 和 CYP2U1 调控肉牛前体脂肪细胞分化。
Mol Cell Probes. 2018 Dec;42:10-17. doi: 10.1016/j.mcp.2018.10.002. Epub 2018 Oct 15.
6
miR-10167-3p targets TCF7L1 to inhibit bovine adipocyte differentiation and promote bovine adipocyte proliferation.miR-10167-3p 通过靶向 TCF7L1 抑制牛脂肪细胞分化并促进牛脂肪细胞增殖。
Genomics. 2024 Sep;116(5):110903. doi: 10.1016/j.ygeno.2024.110903. Epub 2024 Jul 26.
7
MiR-378 Plays an Important Role in the Differentiation of Bovine Preadipocytes.微小RNA-378在牛前体脂肪细胞分化中起重要作用。
Cell Physiol Biochem. 2015;36(4):1552-62. doi: 10.1159/000430318.
8
MicroRNA-224 impairs adipogenic differentiation of bovine preadipocytes by targeting LPL.miRNA-224 通过靶向 LPL 抑制牛前体脂肪细胞的成脂分化。
Mol Cell Probes. 2019 Apr;44:29-36. doi: 10.1016/j.mcp.2019.01.005. Epub 2019 Jan 28.
9
MicroRNA-489-3p promotes adipogenesis by targeting the Postn gene in 3T3-L1 preadipocytes.微小RNA-489-3p通过靶向3T3-L1前脂肪细胞中的Postn基因促进脂肪生成。
Life Sci. 2021 Aug 1;278:119620. doi: 10.1016/j.lfs.2021.119620. Epub 2021 May 15.
10
miR-125a-3p regulates the expression of FSTL1, a pro-inflammatory factor, during adipogenic differentiation, and inhibits adipogenesis in mice.miR-125a-3p 在脂肪生成分化过程中调节促炎因子 FSTL1 的表达,并抑制小鼠的脂肪生成。
FASEB J. 2023 Sep;37(9):e23146. doi: 10.1096/fj.202300851R.

引用本文的文献

1
Transcriptomic Response to Neuromuscular Electrical Stimulation in Muscle, Brain, and Plasma EVs in WT and Klotho-Deficient Mice.野生型和klotho基因缺陷型小鼠肌肉、大脑和血浆细胞外囊泡对神经肌肉电刺激的转录组学反应
Int J Mol Sci. 2025 Aug 14;26(16):7849. doi: 10.3390/ijms26167849.
2
Combined Hyaluronic Acid Nanobioconjugates Impair CD44-Signaling for Effective Treatment Against Obesity: A Review of Comparison with Other Actors.联合透明质酸纳米生物共轭物通过损害CD44信号传导实现对肥胖症的有效治疗:与其他作用物的比较综述
Int J Nanomedicine. 2025 Aug 21;20:10101-10126. doi: 10.2147/IJN.S529250. eCollection 2025.
3
Long-read sequencing uncovers key regulatory genes involved in the differentiation of preadipocytes of Chinese red steppe cattle.
长读长测序揭示了参与中国红草原牛前脂肪细胞分化的关键调控基因。
Sci Rep. 2025 Aug 12;15(1):29459. doi: 10.1038/s41598-025-15106-5.
4
Bta-novel-miR-25336 enhanced adipose differentiation and unsaturated fatty acid synthesis by targeting ACADS in intramuscular adipocytes of river buffalo.Bta-新型-miR-25336通过靶向水牛肌内脂肪细胞中的ACADS来增强脂肪分化和不饱和脂肪酸合成。
BMC Genomics. 2025 Aug 4;26(1):723. doi: 10.1186/s12864-025-11883-5.