Fibroinase plays a vital role in silk gland degeneration by regulating autophagy and apoptosis in the silkworm, Bombyx mori

被引:1
作者
Wang, Zhan
Guo, Pengchao
Hu, Lan
Hua, Guosheng
Yang, Yuanyuan
Zheng, Haogang
Fang, Huan
Xia, Qingyou
Zhao, Ping [1 ]
机构
[1] Southwest Univ, Integrat Sci Ctr Germplasm Creat Western China CHO, Biol Sci Res Ctr, Chongqing 400716, Peoples R China
基金
中国国家自然科学基金;
关键词
Transgenic silkworms; Silk gland; Degeneration; Autophagy; Apoptosis; BOMBYX-MORI; V-ATPASE; CATHEPSIN-B; CELL-DEATH; EXPRESSION; CASPASE; METAMORPHOSIS; PROTEINASE; PROTEASES; GENES;
D O I
10.1016/j.ijbiomac.2024.134312
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The silkworm is an incredibly valuable insect that produces silk through its silk gland. Within this organ, Fibroinase has been identified and named due to its ability to fibroin degradation. The expression of Fibroinase in the silk gland significantly increases during the larval-pupal stage, which might be associated with the degeneration of the silk gland. In this study, Fibroinase was overexpressed and knocked down specifically both in the middle and posterior silk glands, respectively, using transgenic technology. The investigation of silk gland development in these transgenic silkworms showed that Fibroinase plays a direct role in accelerating silk gland degeneration. The staining analyses performed in the silk glands of transgenic silkworms suggest that Fibroinase is involved in the processes of autophagy and apoptosis during silk gland degeneration. Further experiments demonstrated that Fibroinase, acting as a lysosomal regulator, negatively regulates autophagy via the mTOR (mechanistic target of rapamycin) pathway. Moreover, during apoptosis, Fibroinase could activate Caspase3 by increasing the activity of BmCaspase1, ultimately accelerating the apoptosis process. These findings enhance our understanding of the physiological role of Fibroinase in promoting silk gland degeneration, which plays a role in breaking down proteins in the silk gland and coordinating the regulation of autophagy and apoptosis.
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页数:12
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