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Tas2R143 regulates the expression of the Blood-Testis Barrier tight junction protein in TM4 cells through the NF-κB signaling pathway.

Authors :
Wang, Xue
Wang, Jin dan
Li, Xin
Wang, Tianrun
Yao, Jiaqi
Deng, Ruxue
Ma, Wenchang
Liu, Shengjun
Zhu, Zhanbo
Source :
Theriogenology. Oct2024, Vol. 227, p120-127. 8p.
Publication Year :
2024

Abstract

Although bitter receptors, known as Tas2Rs, have been identified in the testes and mature sperm, their expression in testicular Sertoli cells (SCs) and their role in recognizing harmful substances to maintain the immune microenvironment remain unknown. To explore their potential function in spermatogenesis, this study utilized TM4 cells and discovered the high expression of the bitter receptor Tas2R143 in the cells. Interestingly, when the Tas2R143 gene was knocked down for 24 and 48 h, there was a significant downregulation (P < 0.05) in the expression of tight junction proteins (occludin and ZO-1) and NF-κB. Additionally, Western blot results demonstrated that the siRNA-133+NF-κB co-treatment group displayed a significant downregulation (P < 0.05) in the expression of occludin and ZO-1 compared to both the siRNA-133 transfection group and the NF-κB inhibitors treatment group. These findings suggest that Tas2R143 likely regulates the expression of occludin and ZO-1 through the NF-κB signaling pathway and provides a theoretical basis for studying the regulatory mechanism of bitter receptors in the reproductive system, aiming to attract attention to the chemical perception mechanism of spermatogenesis. • Tas2R143 affected to varying degrees the expression of BTB tight junction proteins (occludin, ZO-1) and NF-κB. • Tas2R143 likely regulates the expression of occludin and ZO-1 through the NF-κB signaling pathway in vitro. • This study proposes for the first time that the bitter receptor Tas2R143 is expressed in mouse Sertoli cells (TM4). • This study provides a theoretical basis for studying the regulatory mechanism of bitter receptors in the reproductive system. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0093691X
Volume :
227
Database :
Academic Search Index
Journal :
Theriogenology
Publication Type :
Academic Journal
Accession number :
178810054
Full Text :
https://doi.org/10.1016/j.theriogenology.2024.07.005