Departamento de Fisiología, Pontificia Universidad Católica de Chile, Santiago, Chile.
Biochem Biophys Res Commun. 2011 Jun 17;409(4):603-9. doi: 10.1016/j.bbrc.2011.05.031. Epub 2011 May 12.
Kinetics of permeation through connexin 43-EGFP hemichannels (Cx43-EGFP HCs) were evaluated in divalent cation-free solutions, which enhance HC open probability and thus, allow measurements during initial velocity. Three cations that become fluorescent upon binding to intracellular nucleic acids [ethidium (Etd), propidium (Prd) and 4',6-diamidino-2-phenylindole (DAPI)] and Cx43-EGFP or Cx43 wild type HeLa cell transfectants (Cx43-EGFP- and Cx43-WT-HeLa cells, respectively) were used. Levels of Cx43-EGFP at the cell periphery and rate of dye uptake were directly related. The rate of uptake of each dye reached saturation consistent with a facilitated transport mechanism. Before saturation, the relation between rate of uptake and concentration of each dye was sigmoidal with Hill coefficients >1, indicating positive cooperativity of transport at low concentrations. The maximal rate of Etd uptake was not affected by the presence of DAPI and vice versa, but under each condition the apparent affinity constant of the main permeant molecule increased significantly consistent with competitive inhibition or competition for binding sites within the channel. Moreover, Cx43-EGFP and Cx43-WT HCs had similar permeability properties, indicating that EGFP bound to the C-terminal of Cx43 does not significantly alter the permeability of Cx43 HCs to positively charged molecules. Thus, competitive inhibition of permeation through hemichannels might contribute to cellular retention of essential molecules and/or uptake inhibition of toxic compounds.
在缺乏二价阳离子的溶液中评估了连接蛋白 43-EGFP 半通道(Cx43-EGFP HCs)的渗透动力学,这会增强 HC 开放概率,从而允许在初始速度期间进行测量。使用了三种与细胞内核酸结合后会发荧光的阳离子[乙锭(Etd)、吖啶橙(Prd)和 4',6-二脒基-2-苯基吲哚(DAPI)]以及 Cx43-EGFP 或 Cx43 野生型 HeLa 细胞转染子(Cx43-EGFP-和 Cx43-WT-HeLa 细胞,分别)。细胞边缘的 Cx43-EGFP 水平与染料摄取率直接相关。每种染料的摄取率都达到了饱和,符合易化运输机制。在达到饱和之前,摄取率与每种染料浓度之间的关系呈 S 形,Hill 系数>1,表明在低浓度下运输存在正协同作用。Etd 摄取的最大速率不受 DAPI 的存在影响,反之亦然,但在每种情况下,主要渗透分子的表观亲和力常数都显著增加,这与通道内结合位点的竞争抑制或竞争一致。此外,Cx43-EGFP 和 Cx43-WT HCs 具有相似的通透性特性,表明与 C 末端结合的 EGFP 不会显著改变 Cx43 HCs 对带正电荷分子的通透性。因此,通过半通道渗透的竞争性抑制可能有助于细胞保留必需分子和/或抑制有毒化合物的摄取。