自溶(生物学)
蛋白激酶B
信号转导
PI3K/AKT/mTOR通路
日本使徒
激活剂(遗传学)
生物
细胞生物学
细胞凋亡
化学
生物化学
海参
酶
受体
生态学
作者
Jinghe Sun,Tingting Yan,Xiaoyan Wang,Yimeng Li,Jingfeng Yang
标识
DOI:10.1021/acs.jafc.4c10292
摘要
This study aims to reveal the transduction signaling network that triggers sea cucumber ( Apostichopus japonicus ) autolysis. The tandem mass tag (TMT) proteomics and transcriptomic techniques were used to analyze expression differences between inhibited and activated sea cucumber autolysis. Flow cytometry was used to identify apoptosis. Western blotting and RT-PCR verified the signaling pathway. The results showed that the angiotensin-converting enzyme 2 (ACE 2) activator (diminazene, DIZE) maintained the health of A. japonicus . The ACE 2 inhibitor (captopril, Capt) accelerated the autolysis. Based on the multiomics analysis, the ACE 2 activator activated the downstream NF-κB pathway to prevent the sea cucumber apoptosis. The Capt activated apoptosis initiation. Apoptosis occurred through the regulation of TNF and PI3K-Akt signaling pathways, which downregulate NF-κB. Akt was identified as an intermediate signaling protein downstream of ACE 2 that regulates autolysis in A. japonicus . Compared to A. japonicus in the ultraviolet-irradiated and Capt groups, the Akt inhibitor (perifosine, KRX) significantly reduced the expression of the PI3K-Akt and NF-κB pathways, thereby inhibiting the autolysis process. Additionally, DIZE attenuated ROS levels, thereby inhibiting the autolysis of A. japonicus . This study provides better insight into the autolysis mechanism of A. japonicus .
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