中国畜牧兽医 ›› 2021, Vol. 48 ›› Issue (7): 2349-2357.doi: 10.16431/j.cnki.1671-7236.2021.07.009

• 生理生化 • 上一篇    下一篇

1,25(OH)2D3以双向方式影响猪前体脂肪细胞增殖分化的研究

岳小婧, 张晶, 马姝雯, 曹忻, 卢建雄, 张国华   

  1. 西北民族大学生命科学与工程学院, 兰州 730030
  • 收稿日期:2020-12-14 出版日期:2021-07-20 发布日期:2021-07-15
  • 通讯作者: 张国华 E-mail:381284797@qq.com
  • 作者简介:岳小婧(1989-),女,河北邯郸人,硕士,研究方向:动物脂肪沉积的营养调控机制,E-mail:254907263@qq.com;张晶(1995-),女,甘肃天水人,硕士生,研究方向:动物脂肪沉积的营养调控机制,E-mail:1508783471@qq.com
  • 基金资助:
    国家自然科学基金项目(31860633);国家民委中青年英才计划([2018]98);甘肃省自然科学基金项目(20JR5RA504);西北民族大学中央高校基本科研业务费创新团队项目(31920190001);西北民族大学研究生科研创新项目(Yxm2020129)

1,25(OH)2D3 Affects Proliferation and Differentiation of Porcine Preadipocytes in a Biphasic Manner

YUE Xiaojing, ZHANG Jing, MA Shuwen, CAO Xin, LU Jianxiong, ZHANG Guohua   

  1. College of Life Science and Engineering, Northwest Minzu University, Lanzhou 730030, China
  • Received:2020-12-14 Online:2021-07-20 Published:2021-07-15

摘要: 1,25(OH)2D3是维生素D的主要活性形式,影响人和动物脂肪形成,为探究其在猪脂肪细胞增殖分化中的作用,试验从3~5日龄仔猪皮下脂肪组织分离培养前体脂肪细胞,并以浓度为0、0.1、1、10、100和1 000 nmol/L的1,25(OH)2D3分别处理,在培养的0、1、2、4、6、8和10 d采用MTT比色法检测细胞增殖活性;在诱导分化后0、1、2、4、6、8和10 d,以油红O染色提取法和实时荧光定量PCR检测细胞成脂分化及分化标志基因过氧化物酶体增殖物激活受体γ(PPARγ)和脂肪酸合成酶(FAS)表达。结果显示,0.1和1 nmol/L 1,25(OH)2D3显著促进猪前体脂肪细胞增殖(P<0.05),而浓度为10~100 nmol/L时则抑制细胞增殖(P<0.05);0.1和1 nmol/L 1,25(OH)2D3显著抑制猪前体脂肪细胞分化(P<0.05),降低PPARγ和FAS mRNA表达水平(P<0.05),但在浓度为10和100 nmol/L时,显著促进猪前体脂肪细胞分化(P<0.05),上调PPARγ和FAS mRNA表达(P<0.05);浓度达1 000 nmol/L时,可能对细胞有毒性作用。综合以上结果,低浓度1,25(OH)2D3促进猪前体脂肪细胞增殖,而通过下调PPARγ表达抑制分化;高浓度1,25(OH)2D3抑制猪前体脂肪细胞增殖,通过上调PPARγ表达促进分化。1,25(OH)2D3对猪前体脂肪细胞增殖和分化具有双向作用。

关键词: 1,25(OH)2D3; 猪; 前体脂肪细胞; 增殖; 分化

Abstract: As the main active form of vitamin D,1,25(OH)2D3 affects adipogenesis of humans and animals,but its role in proliferation and differentiation of porcine adipocytes is unclear.To explore the effects of 1,25(OH)2D3 on proliferation and differentiation of porcine preadipocytes,the cells isolated from subcutaneous adipose tissue of 3-5 days piglets were cultured and treated with 0,0.1,1,10,100 and 1 000 nmol/L concentration of 1,25(OH)2D3,respectively.The proliferation of preadipocytes cultured for 0,1,2,4,6,8 and 10 d was detected by MTT method.The differentiation and expression levels of PPARγ and FAS mRNA for the preadipocytes at 0,1,2,4,6,8 and 10 d after inducing-differentiation were determined by oil red O staining and Real-time quantitative PCR,respectively.The results showed that 0.1 and 1 nmol/L 1,25(OH)2D3 significantly promoted proliferation of porcine preadipocytes (P<0.05),but the concentration of 10-100 nmol/L inhibited the cell proliferation (P<0.05).At the concentration of 0.1 and 1 nmol/L,1,25(OH)2D3 markedly inhibited the differentiation of porcine preadipocytes and reduced mRNA expression of PPARγ and FAS (P<0.05).On the contrary,10 and 100 nmol/L 1,25(OH)2D3 significantly enhanced differentiation of porcine preadipocytes and increased mRNA expression of PPARγ and FAS (P<0.05).When the concentration was 1 000 nmol/L,it might be toxic to the cells.These results suggested that low concentration of 1,25(OH)2D3 could promote the proliferation of porcine preadipocytes,but inhibit differentiation through down-regulating PPARγ expression.High concentration of 1,25(OH)2D3 could inhibit the proliferation of the preadipocytes and promote differentiation by up-regulating PPARγ expression.And so,1,25(OH)2D3 affected proliferation and differentiation of porcine preadipocytes in a biphasic manner.

Key words: 1,25(OH)2D3; pig; preadipocyte; proliferation; differentiation

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