Cold stress-induced autophagy and apoptosis disorders are mainly mediated by AMPK/PPAR/PI3K/AKT/mTOR pathways

自噬 PI3K/AKT/mTOR通路 生物 安普克 蛋白激酶B 细胞生物学 氧化应激 细胞凋亡 未折叠蛋白反应 信号转导 内质网 生物化学 蛋白激酶A 激酶
作者
Dongjie Wang,Yao Tian,Qiujie Wang,Yibo Zhang,Bin Ye,Zhiheng Zuo,Jiayang He,Zhengkun Pan,Di Sun,Jixing Zou,Shaolin Xie
出处
期刊:Aquaculture [Elsevier]
卷期号:583: 740574-740574 被引量:4
标识
DOI:10.1016/j.aquaculture.2024.740574
摘要

Under cold stress, the processes of autophagy, apoptosis and energy metabolism are pivotal for sustaining energy and tissue balance. However, the molecular regulatory mechanisms and interactions underlying these processes are still largely unknown. In this study, the molecular mechanisms underlying the regulation of energy homeostasis and tissue homeostasis of Cranoglanis bouderius (13 ± 0.5 g) under cold stress conditions were investigated using histological, metabolomic, and transcriptomic approaches after programmed cooling (25 °C, 20 °C, and 15 °C). Results revealed an uptick in the serum antioxidant activity of C. bouderius during cold stress, contrasted with a decrease in cholesterol levels. Histological assessments revealed extensive damage, marked by evident apoptotic signals, in the gills, liver, and muscles. Transmission electron microscopy and mitochondrial membrane potential analysis also indicated that cold stress induced mitochondrial damage in the liver of C. bouderius, resulting in decreased mitochondrial membrane potential and increased mitochondrial fusion and autophagy. The integrated analysis of metabolomics and transcriptomics suggests that under cold stress, energy homeostasis is primarily regulated by the coordinated action of the AMPK and PPAR signaling pathways, with potential modulation by metabolites like epinephrine. The obstruction of biosynthetic processes is primarily associated with the inhibition of signaling pathways such as PI3K/AKT/mTOR and protein processing in the endoplasmic reticulum. Sustained activation of AMPK alleviates the PI3K/AKT/mTOR-mediated inhibition of autophagy and apoptosis, potentially underpinning the transition from autophagy-mediated apoptosis suppression to apoptosis promotion during cold stress. In summary, these findings elucidate the consequences arising from the altered interactions within the AMPK/PPAR/PI3K/AKT/mTOR pathway under cold stress conditions and offer a theoretical basis for enhancing the ability of fish species to cope with cold stress.
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