ATF6
未折叠蛋白反应
细胞凋亡
p38丝裂原活化蛋白激酶
镉
下调和上调
细胞生物学
内质网
MAPK/ERK通路
毒性
化学
生物
磷酸化
癌症研究
生物化学
有机化学
基因
作者
Sung Woo Lee,Bokyung Kim,Jung Bae Seong,Young-Ho Park,Hong Jun Lee,Dong‐Seok Lee
标识
DOI:10.1093/toxsci/kfad055
摘要
In this study, we examined the mechanisms of cadmium exposure-induced endoplasmic reticulum (ER) stress response and apoptosis in spermatocytes. Responses to cadmium toxicity were investigated using spermatocytes overexpressing p50ATF6, ATF4, and spliced XBP1s, belonging to the 3 unfolded protein response pathways. The ER stress and apoptosis response to cadmium were most strongly stimulated through the activating transcription factor 6 (ATF6) pathway; in contrast, siRNA-induced inhibition of protein expression could reduce apoptosis under stressful conditions. An in vivo experiment using mice confirmed that upregulation of p50ATF6 in the testis increased apoptosis in response to cadmium exposure. Further, when confirming the correlation between ER stress and MAPK in cadmium toxicity, p38 MAPK phosphorylation was strongly regulated by p50ATF6; p-p38 also mediated the activity of p50ATF6. Overall, these findings suggest that modulating the activity of p38 MAPK and p50ATF6 in cadmium exposure-induced toxicity can be considered a potential strategy to treat infertility.
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