Engelmann G L, Worrell R A, Duff R A, Grutkoski P S, Chien K R, Harvey R P
Department of Medicine, Loyola University, Maywood, IL 60153, USA.
Mol Cell Biochem. 1996;157(1-2):87-91. doi: 10.1007/BF00227884.
Recently developed rat heart myocyte cell lines have afforded us the opportunity to evaluate the expression of several transcription factors associated with early cardiac development. These factors include, but are not limited to, Nkx-2.5/Csx, MEF-2C and MLP (Muscle LIM Protein). These factors have been shown to be temporally expressed in pre-cardiac mesenchyme coincident with the earliest stages of heart development. Using the BWEM and CLEM myocyte cell lines as models of the embryonic, committed cardiomyocyte, we have evaluated the basal expression levels of these three genes over multiple passages. Both cell lines express these genes, with MEF-2C being the most abundant based on Northern blot hybridization analyses. Interestingly, as these cells increased their passage number, there was a corresponding increase in their basal expression levels. To evaluate potential 'downstream' effectors of these genes, we examined the basal expression levels of two cardiac-specific genes cTNC and MLC-2v. Transcript levels for both of these contractile filament genes were elevated with passage, suggestive of a inductive process mediated by one or all these three transcription factors. Promoter analysis of MLC-2v expression in the CLEM line shows that this increase is transcriptionally-mediated and the lines retain the necessary regulatory factors to maintain and control the transcription of this gene. Analysis of the dynamics of the regulatory role(s) that these three transcription factors play in cardiac development can now be evaluated in a homogeneous, cell culture system.
最近开发的大鼠心肌细胞系为我们提供了评估几种与心脏早期发育相关的转录因子表达的机会。这些因子包括但不限于Nkx-2.5/Csx、MEF-2C和MLP(肌肉LIM蛋白)。这些因子已被证明在心脏前间充质中与心脏发育的最早阶段同时期表达。利用BWEM和CLEM心肌细胞系作为胚胎期定向心肌细胞的模型,我们评估了这三个基因在多次传代过程中的基础表达水平。两个细胞系都表达这些基因,基于Northern印迹杂交分析,MEF-2C表达量最高。有趣的是,随着这些细胞传代次数的增加,它们的基础表达水平也相应增加。为了评估这些基因潜在的“下游”效应器,我们检测了两个心脏特异性基因cTNC和MLC-2v的基础表达水平。这两个收缩细丝基因的转录水平随着传代而升高,提示这一诱导过程是由这三个转录因子中的一个或全部介导的。对CLEM细胞系中MLC-2v表达的启动子分析表明,这种增加是由转录介导的,并且该细胞系保留了维持和控制该基因转录所需的调节因子。现在可以在一个同质的细胞培养系统中评估这三个转录因子在心脏发育中所起调节作用的动态变化。