He D S, Jiang J X, Taffet S M, Burt J M
Department of Physiology, Arizona Health Sciences Center, University of Arizona, Tucson, AZ, 85724, USA.
Proc Natl Acad Sci U S A. 1999 May 25;96(11):6495-500. doi: 10.1073/pnas.96.11.6495.
Connexin (Cx) 43 and Cx40 are coexpressed in several tissues, including cardiac atrial and ventricular myocytes and vascular smooth muscle. It has been shown that these Cxs form homomeric/homotypic channels with distinct permeability and gating properties but do not form functional homomeric/heterotypic channels. If these Cxs were to form heteromeric channels, they could display functional properties not well predicted by the homomeric forms. We assessed this possibility by using A7r5 cells, an embryonic rat aortic smooth muscle cell line that coexpresses Cxs 43 and 40. Connexons (hemichannels), which were isolated from these cells by density centrifugation and immunoprecipitated with antibody against Cx43, contained Cx40. Similarly, antibody against Cx40 coimmunoprecipitated Cx43 from the same connexon fraction but only Cx40 from Cx (monomer) fractions. These results indicate that heteromeric connexons are formed by these Cxs in the A7r5 cells. The gap junction channels formed in the A7r5 cells display many unitary conductances distinct from homomeric/homotypic Cx43 or Cx40 channels. Voltage-dependent gating parameters in the A7r5 cells are also quite variable compared with cells that express only Cx40 or Cx43. These data indicate that Cxs 43 and 40 form functional heteromeric channels with unique gating and conductance properties.
连接蛋白(Cx)43和Cx40在包括心脏心房和心室肌细胞以及血管平滑肌在内的多种组织中共同表达。研究表明,这些连接蛋白形成具有不同通透性和门控特性的同聚体/同型通道,但不形成功能性的同聚体/异型通道。如果这些连接蛋白要形成异型通道,它们可能会表现出同聚体形式无法很好预测的功能特性。我们通过使用A7r5细胞(一种同时表达Cx43和Cx40的胚胎大鼠主动脉平滑肌细胞系)来评估这种可能性。通过密度离心从这些细胞中分离并使用抗Cx43抗体进行免疫沉淀的连接子(半通道)含有Cx40。同样,抗Cx40抗体从相同的连接子组分中共免疫沉淀出Cx43,但从Cx(单体)组分中仅共免疫沉淀出Cx40。这些结果表明,在A7r5细胞中这些连接蛋白形成了异型连接子。在A7r5细胞中形成的间隙连接通道表现出许多与同聚体/同型Cx43或Cx40通道不同的单位电导。与仅表达Cx40或Cx43的细胞相比,A7r5细胞中的电压依赖性门控参数也有很大差异。这些数据表明,Cx43和Cx40形成了具有独特门控和电导特性的功能性异型通道。