Chronic dietary exposure to glyphosate-induced connexin 43 autophagic degradation contributes to blood-testis barrier disruption in roosters.

Sci Total Environ

College of Veterinary Medicine, Shandong Provincial Key Laboratory of Zoonoses, Shandong Agricultural University, 7 Panhe Street, Tai'an City, Shandong Province 271017, China. Electronic address:

Published: November 2024

AI Article Synopsis

  • Glyphosate (GLY) is the most widely used herbicide, but its chronic exposure leads to significant ecological pollution and male reproductive toxicity in roosters remains unclear.
  • In studies, chronic GLY exposure was found to cause testicular damage and down-regulation of the gap junction gene Connexin 43 (Cx43), essential for the blood-testis barrier (BTB).
  • The degradation of Cx43 was linked to autophagy activation triggered by GLY's interaction with estrogen receptor alpha (ER-α), demonstrating a mechanism for reproductive toxicity in avian species.

Article Abstract

Glyphosate (GLY) is the most universally used herbicide worldwide and its application has caused extensive pollution to the ecological environment. Increasing evidence has revealed the multi-organ toxicity of GLY in different species, but its male reproductive toxicity in avian species remains unknown. Thus, in vivo and in vitro studies were conducted to clarify this issue. Data firstly showed that chronic GLY exposure caused testicular pathological damage. Intriguingly, we identified and verified a marked down-regulation gap junction gene Connexin 43 (Cx43) in GLY-exposed rooster testis by transcriptome analysis. Cx43 generated by Sertoli cells acts as a key component of blood-testis barrier (BTB). To further investigate the cause of GLY-induced downregulation of Cx43 to disrupt BTB, we found that autophagy activation is revealed in GLY-exposed rooster testis and primary avian Sertoli cells. Moreover, GLY-induced Cx43 downregulation was significantly alleviated by ATG5 knockdown or CQ administration, respectively, demonstrating that GLY-induced autophagy activation contributed to Cx43 degradation. Mechanistically, GLY-induced autophagy activation and resultant Cx43 degradation was due to its direct interaction with ER-α. In summary, these findings demonstrate that chronic GLY exposure activates autophagy to induce Cx43 degradation, which causes BTB damage and resultant reproductive toxicity in roosters.

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http://dx.doi.org/10.1016/j.scitotenv.2024.175606DOI Listing

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