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2025年8月5日 星期二
  2018, Vol. 26 Issue (3): 374-382    
  研究论文与报告 本期目录 | 过刊浏览 | 高级检索 |
miR-378基因敲除对小鼠脂肪分解的影响
张园园1,化朝举2,侯欣华2,钮广林2,李奎3,4,唐中林1
1. 中国农业科学院北京畜牧兽医研究所
2.
3. 中国农科院北京畜牧兽医研究所
4. 中国农科院畜牧所
Effects of miR-378 Knockout on Mice (Mus musculus) Lipolysis
2, 2, 2, 2,2, 2
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摘要 在饥饿状态下,机体脂肪内参与能量代谢的许多基因会发生改变来适应环境的变化,从而维持人(Homo sapiens)和动物在没有食物摄入时的生存需要。为了探究miR-378在短期饥饿(24 h)状态下脂肪代谢中发挥的作用,本研究采用野生型和miR-378基因敲除型小鼠(Mus musculus)为材料,分别对小鼠进行正常饲喂及高脂诱导,采集两月龄及高脂诱导两个月的小鼠棕色脂肪、腹股沟脂肪、性腺脂肪、肾周脂肪及皮下脂肪组织,利用qRT-PCR检测脂肪合成和分解相关基因mRNA的表达量,来探讨饥饿状态下miR-378基因敲除对脂肪分解的影响。实验表明在饥饿状态下脂肪合成基因Pparγ表达量降低,而脂肪分解基因激素敏感脂肪酶(hormone sensitive lipase, HSL)、长链脂酰辅酶A合成酶1(acyl-Col synthetase long-chain family member 1, Acsl1)和长链脂酰辅酶A脱氢酶(acyl-Coenzyme A dehydrogenase, long-chain, Acadl)表达量升高,同时miR-378在脂肪中的表达量有所升高。miR-378敲除组与野生组相比在饥饿时脂肪分解标志基因下调。研究结果表明,miR-378可促进禁食状态下脂肪组织的分解,敲除miR-378后抑制禁食状态下脂肪组织的分解。本研究确定了miR-378可作为重要的调节因子影响小鼠脂肪的分解,为人及其他动物脂肪分解的研究提供了重要的理论依据。
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张园园
化朝举
侯欣华
钮广林
李奎
唐中林
关键词 脂肪分解miR-378饥饿小鼠    
Abstract:Under starvation, lots of genes involved in energy metabolism of fat will change in order to adapt to environmental changes for farm animal and human (Homo sapiens). In this study, in order to investigate the regulation role of miR-378 for fat metabolism under short-term (24 h) starvation, wild type (WT) mice and miR-378 knockout (KO) mice (Mus musculus) were used to investigate the fat metabolism difference between normal feeding and high-fat induction conditions. The tissues of brown fat, inguinal fat, gonadal fat, perirenal fat and subcutaneous fat of two months and high-fat induced two months of mice were collected. To explore the effect of miR-378 KO on fat decomposition and fat synthesis under starvation, decomposition related genes were detected by qRT-PCR. The results suggested that the expression of Pparγ was decreased, the expression of hormone sensitive lipase (HSL), long-chain acyl-Coenzyme A dehydrogenase (Acsl1) and acyl-Col synthetase long-chain family member 1 (Acadl) were increased, and also the expression of miR-378 was increased in fat. The expression of fat decomposition maker genes in miR-378 KO were decreased compared with WT. In conclusion, the results demonstrated that miR-378 could promote the decomposition of fat and miR-378 KO inhibit the decomposition under starvation. This study suggests that miR-378 could be a regulatory factor on affecting the fat decomposition in mice, would provide an reference for studying human and other animals fat decomposition.
Key wordsFat Decomposition    miR-378    Starvation    Mice
收稿日期: 2017-07-24      出版日期: 2018-02-14
基金资助:国家自然科学基金;中国农业科学院科技创新工程
通讯作者: 唐中林     E-mail: tangzhonglin@caas.cn
引用本文:   
张园园 化朝举 侯欣华 钮广林 李奎 唐中林. miR-378基因敲除对小鼠脂肪分解的影响[J]. , 2018, 26(3): 374-382.
链接本文:  
http://journal05.magtech.org.cn/Jwk_ny/CN/     或     http://journal05.magtech.org.cn/Jwk_ny/CN/Y2018/V26/I3/374
 
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