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2-氨乙氧基二苯硼酸盐和二苯硼酸酐对 TM₄ 支持细胞间隙连接蛋白 43 组成的缝隙连接的影响。

The effects of 2-aminoethoxydiphenyl borate and diphenylboronic anhydride on gap junctions composed of Connexin43 in TM₄ sertoli cells.

机构信息

Department of Pharmacology, Zhongshan School of Medicine, Sun Yat-Sen University, China.

出版信息

Biol Pharm Bull. 2011;34(9):1390-7. doi: 10.1248/bpb.34.1390.

DOI:10.1248/bpb.34.1390
PMID:21881223
Abstract

2-Aminoethoxydiphenyl borate (2-APB) has recently been demonstrated to inhibit gap junction (GJ) channels, whereas the underlying mechanisms are still unknown. Using mouse TM₄ Sertoli cell which expresses connexin43 (Cx43), we explored the effects of 2-APB and its analogues on dye-coupling through junctional channels formed by Cx43 and on expression of Cx43. Exposure of the cells to 2-APB (1-50 µM) and one of its analogues diphenylboronic anhydride (DPBA) (1-30 µM) for 4 h leads to a significant decrease in dye coupling of GJ in a concentration-dependent manner. The inhibitory effects of 2-APB and DPBA are reversible since decreased GJ coupling resumes after the two compounds are washed out. The disfunction of GJ induced by 2-APB and DPBA is associated with a decrease in total amount of Cx43 protein and number of GJs on the cell membrane. 2-APB and DPBA do not alter Cx43 phosphorylation state and the level of Cx43 mRNA expression. The loss of Cx43 protein is prevented by either lysosomal or proteasomal inhibitor, suggesting that the decrease in Cx43 results from a 2-APB or DPBA-enhanced degradation of Cx43. The present results indicate that 2-APB and DPBA inhibit GJ communication through decreasing Cx43 expression in TM₄ cells.

摘要

2-氨乙基二苯硼酸盐(2-APB)最近被证明可以抑制间隙连接(GJ)通道,但其潜在机制尚不清楚。使用表达连接蛋白 43(Cx43)的小鼠 TM₄ 支持细胞,我们探讨了 2-APB 及其类似物对由 Cx43 形成的缝隙连接通道的染料偶联以及 Cx43 表达的影响。将细胞暴露于 2-APB(1-50 μM)和其类似物二苯硼酐(DPBA)(1-30 μM)4 h 会导致 GJ 染料偶联以浓度依赖性方式显著降低。2-APB 和 DPBA 的抑制作用是可逆的,因为两种化合物被冲洗掉后 GJ 偶联恢复。2-APB 和 DPBA 诱导的 GJ 功能障碍与细胞膜上 Cx43 蛋白总量和 GJ 数量减少有关。2-APB 和 DPBA 不会改变 Cx43 的磷酸化状态和 Cx43 mRNA 表达水平。溶酶体或蛋白酶体抑制剂可防止 Cx43 蛋白丢失,表明 Cx43 的减少是由于 2-APB 或 DPBA 增强了 Cx43 的降解。本研究结果表明,2-APB 和 DPBA 通过降低 TM₄ 细胞中 Cx43 的表达来抑制 GJ 通讯。

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