Blechschmidt Steve, Haufe Volker, Benndorf Klaus, Zimmer Thomas
Institute of Physiology II, Friedrich Schiller University, Kollegiengasse 9, 07743 Jena, Germany.
Prog Biophys Mol Biol. 2008 Oct-Nov;98(2-3):309-18. doi: 10.1016/j.pbiomolbio.2009.01.009. Epub 2009 Jan 29.
In the present study we investigated whether transcription, alternative splicing and developmental regulation of voltage-gated Na(+) channels occur in a species-dependent manner in the mammalian heart. The composition of the Na(+) channel transcript pool including Na(v)1.1-Na(v)1.5 was analysed by RT-PCR in mouse, rat, pig, and human hearts. We found that relative transcript levels of tetrodotoxin (TTX) sensitive channels (Na(v)1.1-Na(v)1.4) decreased with increasing heart size (30% for mouse, 8% for rat, and 4% for pig/human). Considering transcript levels of individual isoforms, human and pig hearts were nearly indistinguishable whereas large differences existed between human and mouse. We also noticed that alternative splicing and age-dependent Na(+) channel expression occurred in a species-dependent manner. Unexpectedly, we even observed gender differences in the cardiac levels of TTX sensitive Na(+) channels in humans. Our data suggest that species differences could underlie published discrepancies on the role of TTX sensitive Na(+) channels in the heart and that the functions of those minor cardiac isoforms in normal and diseased hearts are best studied in larger mammalian animals.
在本研究中,我们调查了电压门控钠通道的转录、可变剪接和发育调控在哺乳动物心脏中是否以物种依赖的方式发生。通过逆转录聚合酶链反应(RT-PCR)分析了小鼠、大鼠、猪和人类心脏中包括Na(v)1.1 - Na(v)1.5在内的钠通道转录本库的组成。我们发现,河豚毒素(TTX)敏感通道(Na(v)1.1 - Na(v)1.4)的相对转录水平随着心脏大小的增加而降低(小鼠为30%,大鼠为8%,猪/人类为4%)。考虑到各个亚型的转录水平,人类和猪的心脏几乎无法区分,而人类和小鼠之间则存在很大差异。我们还注意到可变剪接和年龄依赖性钠通道表达以物种依赖的方式发生。出乎意料的是,我们甚至在人类心脏中观察到了TTX敏感钠通道水平的性别差异。我们的数据表明,物种差异可能是已发表的关于TTX敏感钠通道在心脏中作用的差异的基础,并且那些心脏次要亚型在正常和患病心脏中的功能最好在较大的哺乳动物中进行研究。