Department of Pediatrics, University of Chicago Chicago, IL, USA.
Front Pharmacol. 2013 May 21;4:67. doi: 10.3389/fphar.2013.00067. eCollection 2013.
Connexin43 (Cx43) is widely expressed in many different tissues of the human body. In cells of some organs, Cx43 is co-expressed with other connexins (Cx), including Cx46 and Cx50 in lens, Cx40 in atrium, Purkinje fibers, and the blood vessel wall, Cx45 in heart, and Cx37 in the ovary. Interactions with the co-expressed connexins may have profound functional implications. The abilities of Cx37, Cx45, Cx46, and Cx50 to function in heteromeric gap junction combinations with Cx43 are well documented. Different studies disagree regarding the ability of Cx43 and Cx40 to produce functional heteromeric gap junctions with each other. We review previous studies regarding the heteromeric interactions of Cx43. The possibility of negative functional interactions between the cytoplasmic pore-forming amino-terminal (NT) domains of these connexins was assessed using pentameric connexin sequence-specific NT domain [interfering NT (iNT)] peptides applied to cells expressing homomeric Cx40, Cx37, Cx45, Cx46, and Cx50 gap junctions. A Cx43 iNT peptide corresponding to amino acids 9-13 (Ac-KLLDK-NH2) specifically inhibited the electrical coupling of Cx40 gap junctions in a transjunctional voltage (V j)-dependent manner without affecting the function of homologous Cx37, Cx46, Cx50, and Cx45 gap junctions. A Cx40 iNT (Ac-EFLEE-OH) peptide counteracted the V j-dependent block of Cx40 gap junctions, whereas a similarly charged Cx50 iNT (Ac-EEVNE-OH) peptide did not, suggesting that these NT domain interactions are not solely based on electrostatics. These data are consistent with functional Cx43 heteromeric gap junction formation with Cx37, Cx45, Cx46, and Cx50 and suggest that Cx40 uniquely experiences functional suppressive interactions with a Cx43 NT domain sequence. These findings present unique functional implications about the heteromeric interactions between Cx43 and Cx40 that may influence cardiac conduction in atrial myocardium and the specialized conduction system.
间隙连接蛋白 43(Cx43)广泛表达于人体多种不同组织中。在某些器官的细胞中,Cx43 与其他间隙连接蛋白(Cx)共同表达,包括晶状体中的 Cx46 和 Cx50、心房、浦肯野纤维和血管壁中的 Cx40、心脏中的 Cx45 和卵巢中的 Cx37。与共表达的连接蛋白相互作用可能具有深远的功能意义。Cx37、Cx45、Cx46 和 Cx50 与 Cx43 形成异源间隙连接的能力已有充分的文献记载。不同的研究对于 Cx43 和 Cx40 彼此形成功能性异源间隙连接的能力存在分歧。我们回顾了之前关于 Cx43 异源相互作用的研究。使用五聚体连接蛋白序列特异性氨基末端(NT)结构域 [干扰 NT(iNT)] 肽评估了这些连接蛋白的细胞质孔形成氨基末端(NT)结构域之间可能存在的负性功能相互作用,这些肽应用于表达同源 Cx40、Cx37、Cx45、Cx46 和 Cx50 间隙连接的细胞。与氨基酸 9-13 对应的 Cx43 iNT 肽(Ac-KLLDK-NH2)特异性地以跨连接电压(V j)依赖性方式抑制 Cx40 间隙连接的电偶联,而不影响同源 Cx37、Cx46、Cx50 和 Cx45 间隙连接的功能。Cx40 iNT(Ac-EFLEE-OH)肽拮抗 Cx40 间隙连接的 V j 依赖性阻断,而类似电荷的 Cx50 iNT(Ac-EEVNE-OH)肽则没有,这表明这些 NT 结构域相互作用不仅仅基于静电作用。这些数据与 Cx43 与 Cx37、Cx45、Cx46 和 Cx50 形成功能性异源间隙连接一致,并表明 Cx40 与 Cx43 NT 结构域序列独特地经历功能性抑制相互作用。这些发现提供了关于 Cx43 与 Cx40 之间异源相互作用的独特功能意义,这可能影响心房心肌和特殊传导系统中的心脏传导。