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Fatty acids modulate adipocyte growth and development in pig: An approach from cell culture study

机译:脂肪酸调节脂肪细胞生长和猪的发育:来自细胞培养研究的方法

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We have previously demonstrated that octanoate is necessary for inducing terminal differentiation of pig preadipocytes (Nakajima, I. et al. (2003) Biochem. Biophys. Res. Commun. 309:702-708). The aim of this study is to further investigate the effect of different types of fatty acids (FA) on pig adipocyte differentiation. To assess the role of individual FAs on adipose conversion, preadipocytes (PSPA) which were isolated from subcutaneous tissue of Western crossbred pig were cultured for 10 days in the presence of one of the following FAs; octanoate (C8:0, 1 μM ~ 5 mM), oleate (C18:l, 1 μM ~ 0.2 mM), or arachidonate (C20:4, 1 μM ~ 0.1 mM). We observed that lipid accumulated dose dependently in PSPA cells when treated with either C8:0 or C18:l. PSPA cells treated with C18:l showed the highest TG content with large intracellular lipid droplets among FA at 0.1 mM concentration. RT-PCR analyses revealed that the expression levels of adipogenic markers, such as PPAR p/8, PPARy and CD36, were the lowest in C20:4 treated cells. In contrast to these results of C8:0 and C18:1 treatment, treatment of C20:4 increased the total cell number as well as the proportion of cells in S and G2/M phases of the cell cycle, indicating C20:4 induced cell proliferation rather than adipocyte differentiation. Taken together, our results that the adipose conversion was promoted by the addition of either C8:0 or C18:l to the culture media but not by the addition of C20:4 revealed distinct effects of individual FAs on adipose development in pigs.
机译:我们之前已经证明,辛酸酸盐是诱导猪普雷脂肪细胞的末端分化所必需的(Nakajima,I.等人。(2003)Biochem。生物糖。Res。res.309:702-708)。本研究的目的是进一步研究不同类型脂肪酸(FA)对猪脂肪细胞分化的影响。为了评估单个Fas对脂肪转化的作用,在以下Fas之一存在下,从西杂交猪的皮下组织中分离的前脂肪细胞(PSPA)培养10天;辛酸(C8:0,1μm〜5mm),油脂(C18:L,1μm〜0.2 mm),或腓酮(C20:4,1μm〜0.1mm)。我们观察到用C8:0或C18:L处理时,脂质在PSPA细胞中依赖于PSPA细胞累积剂量。用C18处理的PSPA细胞:L在0.1mm浓度下表现出具有大的细胞内脂质液滴的最高Tg含量。 RT-PCR分析显示,脂肪生成标记物的表达水平,例如PPAR P / 8,PPARAR和CD36,在C20:4处理细胞中最低。与C8:0和C18:1治疗的这些结果相反,C20:4的治疗增加了总细胞数以及细胞周期的S和G2 / M阶段的细胞比例,表明C20:4诱导细胞增殖而不是脂肪细胞分化。我们的结果是通过添加C8:0或C18:L来促进脂肪转化培养培养基,而不是通过添加C20:4揭示了个体Fas对猪脂肪发育的不同影响。

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