Functional expression of gap junction gene Cx43 and the myogenic differentiation of rhabdomyosarcoma cells.

Z. Lin, Z. Zhang, Y. Han, C. Naus, K. Yu, H. Holtzer
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引用次数: 3

Abstract

Rhabdomyosarcoma (RD) cells express low levels of the gap junction protein connexin 43 (Cx43), and its mRNA, and display very weak gap junctional intercellular communication (GJIC) as detected by Cx43 immunofluorescence, slot-blot and dye-transfer methods. These cells grow rapidly and show aberrant and incomplete myogenic differentiation. To investigate the role of gap junctions in these cells, the expression of Cx43 with relation to cell growth and myogenic differentiation in RD single-cell subclones-RDL3 and RDL6 is studied. The subclone RDL3 grows slowly and displays better myogenic differentiation. The expression of Cx43, its mRNA and the GJIC in RDL3 is comparable to that in normal myoblasts. Another subclone RDL6 which grows rapidly, but is poorly differentiated, expresses very low levels of Cx43 and its mRNA, and very weak GJIC. By using the calcium phosphate precipitate transfection technique, a full-length cDNA-encoding Cx43 and a pSV2neo have been introduced into the RDL6 cells. Several stably transfected clones have been obtained. A stable Cx43-transfectant clone RDL6/C-4 expresses high level of Cx43 and its mRNA, and results in dramatic increase of GJIC. These cells grow slowly but display the enhanced myogenic differentiation. A correlation between the down-regulation of Cx43 gene expression and a reduced expression of myogenic differentiation in RD cells is is demonstrated. Forced expression of Cx43 not only inhibits cell growth but also correlates with the improved myogenic differentiation of RD cells.
间隙连接基因Cx43的功能表达与横纹肌肉瘤细胞成肌分化。
横纹肌肉瘤(Rhabdomyosarcoma, RD)细胞表达低水平的间隙连接蛋白连接蛋白43 (Cx43)及其mRNA,并表现出非常弱的间隙连接细胞间通讯(GJIC)。这些细胞生长迅速,表现出异常和不完全的成肌分化。为了研究缝隙连接在这些细胞中的作用,我们研究了Cx43在RD单细胞亚克隆- rdl3和RDL6中表达与细胞生长和成肌分化的关系。亚克隆RDL3生长缓慢,表现出较好的成肌分化。Cx43及其mRNA和GJIC在RDL3中的表达与正常成肌细胞相当。另一个亚克隆RDL6生长迅速,但分化较差,表达极低水平的Cx43及其mRNA, GJIC非常弱。利用磷酸钙沉淀转染技术,将编码Cx43和pSV2neo的全长cdna导入RDL6细胞。已经获得了几个稳定转染的克隆。一个稳定的Cx43-转染克隆RDL6/C-4表达高水平的Cx43及其mRNA,导致GJIC急剧增加。这些细胞生长缓慢,但表现出增强的成肌分化。研究证实,在RD细胞中,Cx43基因表达下调与肌源性分化表达减少之间存在相关性。强迫表达Cx43不仅抑制细胞生长,而且与RD细胞肌源性分化的改善有关。
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