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

Yan Yang, Ming-Hui Cao, Qin Wang, Dong-Dong Yuan, Li Li, Liang Tao

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

Journal Article: Biological & Pharmaceutical Bulletin (impact factor: 1.81). 01/2011; 34(9):1390-7.

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.

Source: PubMed

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Keywords

2-Aminoethoxydiphenyl borate
 
analogues diphenylboronic anhydride
 
cell membrane
 
Cx43 mRNA expression
 
Cx43 phosphorylation state
 
Cx43 protein
 
Cx43 results
 
decreasing Cx43 expression
 
DPBA-enhanced degradation
 
dye coupling
 
dye-coupling
 
GJ coupling resumes
 
GJ induced
 
inhibitory effects
 
junctional channels
 
mouse TM₄ Sertoli cell
 
significant decrease
 
TM₄ cells
 
two compounds
 
underlying mechanisms