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首页> 外文期刊>International Journal of Cardiology >Effect of bone morphogenetic protein-4 on cardiac differentiation from mouse embryonic stem cells in serum-free and low-serum media.
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Effect of bone morphogenetic protein-4 on cardiac differentiation from mouse embryonic stem cells in serum-free and low-serum media.

机译:骨形态发生蛋白4对无血清和低血清培养基中小鼠胚胎干细胞心脏分化的影响。

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摘要

In spite of previous reports, the precise role of bone morphogenetic proteins (BMPs) on cardiomyocyte differentiation, especially in the absence or presence of minimum amount of serum in culture medium is still unclear. So, the aim of the present study was to investigate the effect of BMP-4 on mouse embryonic stem cells (ESCs)-derived cardiomyocyte differentiation in serum-free and low-serum media. The mouse ESCs differentiation to cardiomyocytes was induced by embryoid bodies' (EBs') development through hanging drop, suspension and plating stages. Different models of differentiation were designed according to addition of fetal bovine serum (FBS) or knockout serum replacement (KoSR) to the medium of three stages. 10 ng/ml BMP-4 was added throughout the suspension period. Up to 30 days after plating, contraction and beating frequency were monitored and evaluated daily. The growth characteristics of cardiomyocytes were assessed by cardioactive drugs, immunocytochemistry, transmission electron microscopy (TEM) and reverse transcription-polymerase chain reaction (RT-PCR). In the complete absence of serum, neither control nor BMP-4 treated groups resulted in cardiac differentiation. Addition of FBS to hanging drop stage resulted in the appearance of beating cardiac clusters in some BMP-4 treated EBs. In the best designed differentiation model in which only hanging drop and the first 24 h of plating stage was carried out at the presence of FBS, the BMP-4 treatment resulted in cardiac differentiation in EBs characterized by positive immunostaining for the applied antibodies, chronotropic response to the cardioactive drugs and cardiac-specific genes expression at different developmental stages. These cardiomyocytes showed immature myofibrils and numerous intercellular junctions. In conclusion, BMP-4 is unable to induce cardiomyocyte differentiation from mouse ESCs in serum-free models, and at least small amount of FBS in hanging drop stage is necessary. Furthermore, serum factors are not strictly necessary after the initial activation, but they do favor a better differentiation of cardiomyocytes.
机译:尽管有先前的报道,但尚不清楚骨形态发生蛋白(BMP)在心肌细胞分化中的确切作用,尤其是在培养基中不存在或存在少量血清的情况下。因此,本研究的目的是研究BMP-4在无血清和低血清培养基中对小鼠胚胎干细胞(ESCs)衍生的心肌细胞分化的影响。小鼠胚胎干细胞向心肌细胞的分化是由类胚体(EBs)通过悬垂,悬浮和铺板阶段的发育诱导的。根据在三个阶段的培养基中添加胎牛血清(FBS)或敲除血清替代品(KoSR),设计了不同的分化模型。在整个悬浮过程中加入10 ng / ml BMP-4。电镀后长达30天,每天监测和评估其收缩和跳动频率。通过心脏活性药物,免疫细胞化学,透射电子显微镜(TEM)和逆转录聚合酶链反应(RT-PCR)评估心肌细胞的生长特征。在完全没有血清的情况下,对照组和BMP-4处理组均未导致心脏分化。在垂降阶段添加FBS会导致在某些BMP-4处理过的EB中出现跳动的心脏簇。在最佳设计的分化模型中,只有在FBS存在的情况下才进行悬滴和接种前24小时,BMP-4处理可导致EB的心脏分化,其特征在于所应用抗体的阳性免疫染色,变时反应在不同发育阶段对心脏活性药物和心脏特异性基因表达的影响。这些心肌细胞显示出未成熟的肌原纤维和许多细胞间连接。总之,在无血清模型中,BMP-4不能诱导小鼠ESC分化为心肌细胞,在垂降阶段至少需要少量FBS。此外,在初始激活后,血清因子并非绝对必要,但它们确实有助于更好地分化心肌细胞。

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