首页> 外文会议>ICoMST 2011;International conference of meat science and technology >Fatty acids modulate adipocyte growth and development in pig: An approach from cell culture study
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Fatty acids modulate adipocyte growth and development in pig: An approach from cell culture study

机译:脂肪酸调节猪脂肪细胞的生长和发育:细胞培养研究的一种方法

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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:我们先前已经证明辛酸对于诱导猪前脂肪细胞的终末分化是必需的(Nakajima,I。等人(2003)Biochem.Biophys.Res.Commun.309:702-708)。这项研究的目的是进一步研究不同类型的脂肪酸(FA)对猪脂肪细胞分化的影响。为了评估单个FA在脂肪转化中的作用,在以下一种FA的存在下,将从西方杂交猪皮下组织分离的前脂肪细胞(PSPA)培养10天。辛酸酯(C8:0,1μM〜5 mM),油酸酯(C18:l,1μM〜0.2 mM)或花生四烯酸酯(C20:4,1μM〜0.1 mM)。我们观察到,当用C8:0或C18:1处理时,脂质在PSPA细胞中累积剂量依赖性。在0.1 mM浓度的FA中,用C18:1处理的PSPA细胞显示出最高的TG含量和较大的细胞内脂质滴。 RT-PCR分析显示,成脂标记物(例如PPAR p / 8,PPARy和CD36)的表达水平在C20:4处理的细胞中最低。与C8:0和C18:1处理的这些结果相反,C20:4的处理增加了细胞周期的S和G2 / M期的总细胞数以及细胞比例,表明C20:4诱导了细胞增殖而不是脂肪细胞分化。两者合计,我们的结果是通过向培养基中添加C8:0或C18:1而不是通过添加C20:4来促进脂肪转化,这揭示了各个FA对猪脂肪发育的显着影响。

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