Clinic for Paediatric Cardiology, Heart Centre, University of Leipzig, Strümpellstraße. 39, 04289, Leipzig, Germany.
Naunyn Schmiedebergs Arch Pharmacol. 2011 Apr;383(4):331-46. doi: 10.1007/s00210-011-0603-4. Epub 2011 Feb 12.
Electrical intercellular communication in the heart allows the propagation of an action potential from cell to cell. This is realized by low-ohmic cell-to-cell channels, the gap junction channels, which are dodecameric proteins consisting of two hexameric hemichannels. Each of the neighbouring cell provides one hemichannel, which consists of six connexins. In the heart, the connexin isoforms Cx43, Cx40 and Cx45 are present with Cx43 being the most abundant isoform. This intercellular communication is regulated acutely by control of the gap junction conductance and chronically by control of the connexin expression. The short half-life time of Cx43 indicates the permanent adaptation of cell communication to the actual requirements. β-Adrenoceptor stimulation enhances Cx40- but reduces Cx45-conductance, while Cx43 channels in most species do not seem to be acutely affected by β-adrenoceptor signalling. In contrast, chronic exposure to β-adrenergic stimulants activates protein kinase A and the mitogenic-activated protein kinase cascade (including protein 38 (p38), mitogenic-activated protein kinase kinase 1, extracellular signal-regulated kinase (ERK)1/2 and c-JUN NH(2) terminal kinase (JNK)), the calcineurin pathway, translocation of activator protein 1 (AP1), CRE-binding protein and nuclear factor of activated T cells, finally leading to enhanced Cx43-mRNA and Cx43-protein expression together with Cx43 phosphorylation, but does not affect Cx40. α-Adrenoceptors also play a role in controlling cardiac intercellular communication: α-adrenergic stimulation acutely uncouples the cells, while a chronic stimulation enhances Cx43 expression via protein kinase C, p38, ERK1/2, JNK, c-fos and AP1, but does not alter Cx40 expression. While general cardiac protein synthesis, e.g. of β-actin, is controlled via α(1A)-adrenoceptors, Cx43 expression is regulated via α(1D)-adrenoceptors. However, α-adrenoceptor density in the heart varies among species, with high abundance in rat heart and low in human heart. Acute α-adrenergic stimulation, e.g. during ischemia, can lead to uncoupling and facilitates re-entrant arrhythmia. Chronic adrenergic upregulation of Cx43 expression seems to be involved in cardiac hypertrophy. In maladaptive hypertrophy, the enhanced Cx43 is increasingly incorporated in the lateral membrane of the cells rather at the cell poles, which may mean a gap junction disarray. This could-together with a mismatch in cell size and coupling-contribute to arrhythmogenesis. Thus, cardiac adrenoceptors are directly involved in the control of intercellular electrical communication and thus probably are a critical factor in the maintenance of regular cell-to-cell conduction and of the cardiac electrical networking. They probably are involved in the formation of an arrhythmogenic substrate in certain heart diseases.
心脏中的电细胞间通讯允许动作电位从一个细胞传播到另一个细胞。这是通过低欧姆细胞间通道,缝隙连接通道来实现的,缝隙连接通道由两个六聚体半通道组成的十二聚体蛋白。每个相邻的细胞提供一个半通道,由六个连接蛋白组成。在心脏中,存在连接蛋白亚型 Cx43、Cx40 和 Cx45,其中 Cx43 是最丰富的亚型。这种细胞间通讯被缝隙连接电导的急性控制和连接蛋白表达的慢性控制所调节。Cx43 的半衰期短表明细胞通讯的永久适应实际需要。β-肾上腺素能受体刺激增强 Cx40-但降低 Cx45-电导,而大多数物种中的 Cx43 通道似乎不受 β-肾上腺素能受体信号的急性影响。相比之下,慢性暴露于β-肾上腺素能刺激物激活蛋白激酶 A 和有丝分裂原激活的蛋白激酶级联(包括蛋白 38(p38)、有丝分裂原激活的蛋白激酶激酶 1、细胞外信号调节激酶 (ERK)1/2 和 c-JUN NH2 末端激酶 (JNK))、钙调神经磷酸酶途径、激活蛋白 1 (AP1)的易位、CRE 结合蛋白和激活 T 细胞的核因子,最终导致 Cx43-mRNA 和 Cx43-蛋白表达增强,同时 Cx43 磷酸化,但不影响 Cx40。α-肾上腺素能受体也在控制心脏细胞间通讯中发挥作用:α-肾上腺素能刺激急性解偶联细胞,而慢性刺激通过蛋白激酶 C、p38、ERK1/2、JNK、c-fos 和 AP1 增强 Cx43 表达,但不改变 Cx40 表达。虽然一般的心脏蛋白合成,如 β-肌动蛋白,是通过 α(1A)-肾上腺素受体控制的,但 Cx43 表达是通过 α(1D)-肾上腺素受体调节的。然而,心脏中的 α-肾上腺素能受体密度在物种间存在差异,在大鼠心脏中丰富,在人类心脏中较低。急性 α-肾上腺素能刺激,如在缺血期间,可导致解偶联并促进折返性心律失常。Cx43 表达的慢性肾上腺素能上调似乎与心脏肥大有关。在适应性肥大中,增强的 Cx43 越来越多地整合到细胞的侧膜中,而不是在细胞极,这可能意味着缝隙连接排列紊乱。这可能与细胞大小和偶联的不匹配一起导致心律失常的发生。因此,心脏肾上腺素能受体直接参与细胞间电通讯的控制,因此可能是维持细胞间正常传导和心脏电网络的关键因素。它们可能参与了某些心脏病中致心律失常基质的形成。