中国农业科技导报 ›› 2024, Vol. 26 ›› Issue (2): 100-108.DOI: 10.13304/j.nykjdb.2022.0930

• 生物技术 生命科学 • 上一篇    

绵羊前体脂肪细胞分化过程中关键基因时序表达特征研究

杨广军1,2(), 廖媛3, 张志超2, 钟荣珍4, 段子渊2()   

  1. 1.宁夏大学农学院,银川 750021
    2.中国科学院遗传与发育生物学研究所,北京 100101
    3.西南大学家蚕基因组生物学国家重点实验室,重庆 400715
    4.中国科学院东北地理与农业生态研究所,长春 130062
  • 收稿日期:2022-10-29 接受日期:2023-01-12 出版日期:2024-02-15 发布日期:2024-02-04
  • 通讯作者: 段子渊
  • 作者简介:杨广军 E-mail:guangjuny1011@163.com
  • 基金资助:
    中国科学院战略性先导科技专项(A类)(XDA260040305)

Characteristics of Temporal Expression of Key Genes During Differentiation from Sheep Preadipocyte

Guangjun YANG1,2(), Yuan LIAO3, Zhichao ZHANG2, Rongzhen ZHONG4, Ziyuan DUAN2()   

  1. 1.School of Agriculture,Ningxia University,Yinchuan 750021,China
    2.Institute of Genetics and Developmental Biology,Chinese Academy of Sciences,Beijing 100101,China
    3.State Key Laboratory of Silkworm Genome Biology,Southwest University,Chongqing 400715,China
    4.Northeast Institute of Geography and Agroecology,Chinese Academy of Sciences,Changchun 130062,China
  • Received:2022-10-29 Accepted:2023-01-12 Online:2024-02-15 Published:2024-02-04
  • Contact: Ziyuan DUAN

摘要:

为分析绵羊前体脂肪细胞在成脂分化过程中关键基因的表达规律及特点,以3T3-L1细胞系为参照,选取出生20 d的呼伦贝尔羊母羔羊,利用组织块消化法从其尾部脂肪组织中分离前体脂肪细胞,建立原代细胞系。利用鸡尾酒法分别对3T3-L1细胞系和绵羊前体脂肪细胞系进行诱导分化,采用实时荧光定量PCR检测诱导分化过程中关键基因的时序表达。结果显示,绵羊前体脂肪细胞成脂分化用时更长,诱导分化16 d后依然有部分细胞具有分化能力。基因时序表达分析表明,DLK1SREBP1ACC1FASN基因的时序表达趋势在2类细胞中基本一致;ZFP423ADIPOQC/EBPα基因的表达时序在2类细胞系中高度相似;而PPARγFABP4LPLHSL基因在2类细胞系中的时序表达趋势差异较大。相比3T3-L1细胞系,绵羊前体脂肪细胞中ZFP423ADIPOQC/EBPαFABP4的相对表达量在诱导分化中、后期仍然处于较高水平,PPARγLPLHSL的相对表达量呈现持续增长趋势,表明绵羊前体脂肪细胞的成脂分化具有自身特点。根据基因表达情况推测,绵羊前体脂肪细胞诱导分化16 d后通过外界环境摄取脂肪酸合成甘油三酯并沉积于细胞,这种较强的吸收外界环境脂肪酸的能力可能是本土绵羊皮下脂肪过度沉积的原因之一。综上所述,对绵羊脂肪代谢的相关研究以绵羊脂肪细胞为模型更加合理,为绵羊脂肪代谢研究提供了可靠的试验模型。

关键词: 绵羊, 前体脂肪细胞, 成脂分化, 基因时序表达

Abstract:

To analyze the expression pattern and characteristics of key genes in sheep preadipocytes during adipogenic differentiation, 3T3-L1 cell line was selected as reference, the preadipocytes were isolate from the tail adipose tissue of female lambs from Hulun Buir sheep 20-day after birth using tissue digestion method and prepared into primary cell line. The 3T3-L1 cell line and sheep preadipocyte cells were induced to differentiate into mature adipocyte by cocktail method, and the temporal expressions of key genes during differentiation were detected by real-time fluorescence quantitative PCR. The results showed that the adipogenic differentiation of sheep precursor adipocytes took longer, and some cells still had differentiation ability after 16 d of induction. The patterns of temporal expression indicate that the expressions of DLK1SREBP1ACC1 and FASN were basically consistence both in the sheep preadipocytes and 3T3-L1 cell lines, the expression trends of ZFP423ADIPOQ and C/EBPα were highly similar, however, the genes of PPARγFABP4LPL and HSL were different. Compared with 3T3-L1 cell line, the relative expression levels of ZFP423ADIPOQC/EBPα and FABP4 in sheep preadipocytes still remained at a high level in the middle and late stages of induced differentiation, and the relative expressions of PPARγLPL and HSL showed a continuous increase trend, which illustrated that sheep preadipocytes had its own characteristics in adipogenic differentiation. It was speculated that the cells from the sheep adipocytes synthesized triglycerides and then deposited in mature adipocytes through ingesting fatty acids from the external environment after 16 d of induction according to the expression of related genes. It indicated that sheep adipose cells had strong ability to absorb external fatty acids, which might be one of reasons for the excessive deposition of subcutaneous fat in native sheep. So the sheep adipocyte was more suitable as a cell model in research of sheep fat metabolism, which provided reliable experimental model for research of sheep fat metabolism.

Key words: sheep, preadipocytes, adipogenic differentiation, gene temporal expression

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