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猪前体脂肪细胞与肌肉卫星细胞体外共培养的增殖与分化特性。

The proliferation and differentiation characteristics of co-cultured porcine preadipocytes and muscle satellite cells in vitro.

机构信息

College of Animal Science and Technology, Northwest A&F University, Yangling 712100, Shaanxi, China.

出版信息

Mol Biol Rep. 2013 Apr;40(4):3197-202. doi: 10.1007/s11033-012-2395-0. Epub 2012 Dec 29.

DOI:10.1007/s11033-012-2395-0
PMID:23271122
Abstract

To explore the proliferation and differentiation characteristics of co-cultured porcine preadipocytes and muscle satellite cells, preadipocytes and muscle satellite cells were isolated from the healthy nascent landrace. Oil Red O stain and desmin immunohistochemistry were used to identify the two solo-cultured cells. Methyl thiazolyl tetrazolium (MTT) colorimetric assay was used to detect the proliferation characteristic of co-cultured cells, and the expression level of differentiation marker genes lipoprotein lipase (LPL), peroxisome proliferator-activated receptors (PPARγ), myogenic factor 5 (Myf5), myogenin (MyoG) were analyzed with reverse transcription PCR (RT-PCR) and western blot. The success of co-culture system was proved. In the co-cultured cells, slight lipid droplets were observed and appeared more slowly. The polykaryocytes fused into myotubes in co-cultured cells were less and relatively slow than that in solo myocytes. After fusion, the proliferation rate of co-cultured cells was higher than that in the solo-cultured muscle satellite cells (P < 0.01), and the duration were also longer. On day 5 and 10, the expression of the marker genes in earlier stage of cell differentiation (LPL and Myf5) were lower than those in the solo-cultured cells (P < 0.01) (except LPL gene at day 5). Moreover, the expression of intermediate and advanced stages' maker genes (PPARγ2 and MyoG) were hardly detectable at day 5, but increased significantly on day 10 (P < 0.01). These results confirm that the co-culture system could facilitate the cells' growth and proliferation, meanwhile, inhibited the cell differentiation.

摘要

为了探索共培养猪前体脂肪细胞和肌肉卫星细胞的增殖和分化特性,从健康的新生长白猪中分离前体脂肪细胞和肌肉卫星细胞。油红 O 染色和结蛋白免疫组织化学用于鉴定两种单独培养的细胞。噻唑蓝(MTT)比色法检测共培养细胞的增殖特性,并用逆转录聚合酶链反应(RT-PCR)和蛋白质印迹法分析分化标记基因脂蛋白脂肪酶(LPL)、过氧化物酶体增殖物激活受体(PPARγ)、肌生成因子 5(Myf5)、肌细胞生成素(MyoG)的表达水平。证明了共培养系统的成功。在共培养细胞中,观察到少量脂滴,且出现较慢。与单独肌细胞相比,共培养细胞中的多核细胞融合形成肌管的数量较少且相对较慢。融合后,共培养细胞的增殖率高于单独培养的肌肉卫星细胞(P<0.01),且持续时间也更长。在第 5 天和第 10 天,细胞分化早期(LPL 和 Myf5)的标记基因表达低于单独培养细胞(P<0.01)(第 5 天除外 LPL 基因)。此外,中间和晚期标记基因(PPARγ2 和 MyoG)的表达在第 5 天几乎检测不到,但在第 10 天显著增加(P<0.01)。这些结果证实,共培养系统可以促进细胞的生长和增殖,同时抑制细胞分化。

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