摘要
以HSPA1L基因敲除(HSPA1L^(-/-))雄性小鼠为研究对象,观察甲状腺组织形态和细胞凋亡情况,分析Caspase-3蛋白表达,探讨叔丁醇(TBA)的毒性以及HSPA1L在此过程中的作用机制.结果表明,HSPA1L^(-/-)小鼠甲状腺的重量随TBA剂量增加而显著降低(P<0.05);甲状腺上皮滤泡细胞随TBA剂量增加而增大,高剂量组甲状腺滤泡甚至发生融合现象;甲状腺细胞凋亡增强,甲状腺组织Caspase-3表达量极显著增加(P<0.01).HSPA1L^(-/-)小鼠对TBA暴露更为敏感,TBA造成的伤害显著增强,提示HSPA1L可能通过负调控Caspase-3表达,抑制细胞凋亡,维持细胞稳态.
In this study,male mice with HSPA1L gene deletion were studied tOobserve the thyroid tissue morphology and cell apoptosis,analyze the expression of Caspase-3 protein,and explore the toxicity of TBA and the potential mechanism of HSPA1L.The results showed that the thyroid weight of HSPA1L^(-/-)mice decrease significantly with the increase of TBA dose(P<0.05).Thyroid epithelial follicular cells enlarged with the increase of TBA dose,and follicular fusion even occured in the high dose group.Cell apoptos of thyroid tissue were significantly enhanced.The expression of Caspase-3 in thyroid tissue was very significantly increased(P<0.01).This study showed that HSPA1L^(-/-)mice were more sensitive to TBA exposure,and the damage caused by TBA was significantly enhanced,suggesting that HSPA1L had strong protective effects on inhibiting apoptosis and maintaining cell homeostasis.
作者
董思林
赵振军
石慧
DONG Si-lin;ZHAO Zhen-jun;SHI Hui(College of Life Sciences,Yantai University,Yantai 264005,Shandong,China)
出处
《西北师范大学学报(自然科学版)》
CAS
2024年第3期48-54,共7页
Journal of Northwest Normal University(Natural Science)
基金
国家重点研发计划项目(2018YFC1003600)。