Zahradka P, Harris K D, Triggs-Raine B, Lamontagne G, Leblanc N
Division of Cardiovascular Sciences, St. Boniface General Hospital Research Centre.
Mol Cell Biochem. 1995 Apr 12;145(1):39-44. doi: 10.1007/BF00925711.
Irregularities in K+ currents form the basis of several cardiovascular dysfunctions, among which are arrhythmias and vasospasms. The developmental regulation of voltage-gated K+ channels, however, has been difficult to study. A novel approach was therefore employed to examine these channels in muscle tissue. Primers for a PCR-based analysis were designed using published nucleic acid sequences for voltage-gated K+ channels. Final selection of the primer pairs was based on the homology present in the S4 and H5 transmembrane domains. A specific band was amplified with these primers using RNA isolated from both rat A10 vascular smooth muscle cells and rat heart tissue.
钾离子电流的异常是多种心血管功能障碍的基础,其中包括心律失常和血管痉挛。然而,电压门控钾通道的发育调控一直难以研究。因此,采用了一种新方法来检测肌肉组织中的这些通道。基于已发表的电压门控钾通道核酸序列设计了用于聚合酶链反应(PCR)分析的引物。引物对的最终选择基于S4和H5跨膜结构域中的同源性。使用从大鼠A10血管平滑肌细胞和大鼠心脏组织中分离的RNA,用这些引物扩增出了一条特异性条带。