Division of Neonatology, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.
Physiol Genomics. 2010 Oct;42A(2):131-40. doi: 10.1152/physiolgenomics.00049.2010. Epub 2010 Aug 3.
Spontaneous diastolic depolarization in the sinoatrial (SA) node enables it to serve as pacemaker of the heart. The variable cell morphology within the SA node predicts that ion channel expression would be heterogeneous and different from that in the atrium. To evaluate ion channel heterogeneity within the SA node, we used fluorescent in situ hybridization to examine ion channel expression in the ferret SA node region and atrial appendage. SA nodal cells were distinguished from surrounding cardiac myocytes by expression of the slow (SA node) and cardiac (surrounding tissue) forms of troponin I. Nerve cells in the sections were identified by detection of GAP-43 and cytoskeletal middle neurofilament. Transcript expression was characterized for the 4 hyperpolarization-activated cation channels, 6 voltage-gated Na(+) channels, 3 voltage-gated Ca(2+) channels, 24 voltage-gated K(+) channel α-subunits, and 3 ancillary subunits. To ensure that transcript expression was representative of protein expression, immunofluorescence was used to verify localization patterns of voltage-dependent K(+) channels. Colocalizations were performed to observe any preferential patterns. Some overlapping and nonoverlapping binding patterns were observed. Measurement of different cation channel transcripts showed heterogeneous expression with many different patterns of expression, attesting to the complexity of electrical activity in the SA node. This study provides insight into the possible role ion channel heterogeneity plays in SA node pacemaker activity.
窦房结中的自发性舒张去极化使它能够充当心脏的起搏器。窦房结内可变的细胞形态表明,离子通道的表达将是异质的,与心房不同。为了评估窦房结内的离子通道异质性,我们使用荧光原位杂交技术检查了雪貂窦房结区域和心房附件中的离子通道表达。通过慢(窦房结)和心脏(周围组织)形式的肌钙蛋白 I 的表达,将窦房结细胞与周围的心肌细胞区分开来。通过检测 GAP-43 和细胞骨架中间神经丝来识别切片中的神经细胞。对 4 种超极化激活阳离子通道、6 种电压门控 Na+通道、3 种电压门控 Ca2+通道、24 种电压门控 K+通道α亚基和 3 种辅助亚基的转录表达进行了特征描述。为了确保转录表达代表蛋白质表达,我们使用免疫荧光来验证电压依赖性 K+通道的定位模式。进行共定位以观察任何优先模式。观察到一些重叠和不重叠的结合模式。对不同阳离子通道转录本的测量显示出异质表达,具有许多不同的表达模式,证明了窦房结电活动的复杂性。这项研究为离子通道异质性在窦房结起搏活动中的可能作用提供了深入了解。