Zhong Guoqiang, Akoum Nazem, Appadurai Daniel A, Hayrapetyan Volodya, Ahmed Osman, Martinez Agustin D, Beyer Eric C, Moreno Alonso P
Department of Cardiology, First Affiliated Hospital of Guangxi Medical UniversityGuangxi, China.
University Medical Center, University of WashingtonSeattle, WA, United States.
Front Physiol. 2017 May 29;8:346. doi: 10.3389/fphys.2017.00346. eCollection 2017.
In cardiac tissues, the expression of multiple connexins (Cx40, Cx43, Cx45, and Cx30.2) is a requirement for proper development and function. Gap junctions formed by these connexins have distinct permeability and gating mechanisms. Since a single cell can express more than one connexin isoform, the formation of hetero-multimeric gap junction channels provides a tissue with an enormous repertoire of combinations to modulate intercellular communication. To study further the perm-selectivity and gating properties of channels containing Cx43 and Cx45, we studied two monoheteromeric combinations in which a HeLa cell co-transfected with Cx43 and Cx45 was paired with a cell expressing only one of these connexins. Macroscopic measurements of total conductance between cell pairs indicated a drastic reduction in total conductance for mono-heteromeric channels. In terms of Vj dependent gating, Cx43 homomeric connexons facing heteromeric connexons only responded weakly to voltage negativity. Cx45 homomeric connexons exhibited no change in Vj gating when facing heteromeric connexons. The distributions of unitary conductances (γj) for both mono-heteromeric channels were smaller than predicted, and both showed low permeability to the fluorescent dyes Lucifer yellow and Rhodamine123. For both mono-heteromeric channels, we observed flux asymmetry regardless of dye charge: flux was higher in the direction of the heteromeric connexon for MhetCx45 and in the direction of the homomeric Cx43 connexon for MhetCx43. Thus, our data suggest that co-expression of Cx45 and Cx43 induces the formation of heteromeric connexons with greatly reduced permeability and unitary conductance. Furthermore, it increases the asymmetry for voltage gating for opposing connexons, and it favors asymmetric flux of molecules across the junction that depends primarily on the size (not the charge) of the crossing molecules.
在心脏组织中,多种连接蛋白(Cx40、Cx43、Cx45和Cx30.2)的表达是正常发育和功能所必需的。这些连接蛋白形成的间隙连接具有不同的通透性和门控机制。由于单个细胞可以表达不止一种连接蛋白异构体,异源多聚体间隙连接通道的形成使组织拥有大量组合方式来调节细胞间通讯。为了进一步研究包含Cx43和Cx45的通道的通透选择性和门控特性,我们研究了两种单异源组合,即将同时转染了Cx43和Cx45的HeLa细胞与仅表达其中一种连接蛋白的细胞配对。对细胞对之间总电导的宏观测量表明,单异源通道的总电导急剧降低。就电压依赖性门控而言,面对异源连接子的Cx43同源连接子仅对电压负值有微弱反应。当面对异源连接子时,Cx45同源连接子在电压门控方面没有变化。两种单异源通道的单位电导(γj)分布均小于预期,并且对荧光染料路西法黄和罗丹明123的通透性都很低。对于两种单异源通道,无论染料电荷如何,我们都观察到通量不对称:对于MhetCx45,通量在异源连接子方向上更高,而对于MhetCx43,通量在同源Cx43连接子方向上更高。因此,我们的数据表明,Cx45和Cx43的共表达诱导了通透性和单位电导大大降低的异源连接子的形成。此外,它增加了相对连接子电压门控的不对称性,并且有利于分子跨连接的不对称通量,这主要取决于穿越分子的大小(而非电荷)。