丝素蛋白分泌缺陷蚕突变体的自噬缺陷。

Jianhua Xia, Haiqin Chen, Yuying Wang, Wenbo Hu, Kaiyu Guo, Qingqing Linghu, Pengchao Guo, Xin Wang, Qingyou Xia, Ioannis P Nezis, Ping Zhao, Zhaoming Dong, Yan Zhang
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引用次数: 0

摘要

家蚕是生产蚕丝的重要经济昆虫。它的丝腺负责丝蛋白的合成和分泌。蚕蛹裸蛹(Nd)是蚕丝蛋白重链突变株,出现严重的萎缩、后丝腺(PSG)变性和丝素蛋白分泌异常,从而产丝少或不产丝。本研究发现,自噬标志物Atg8-PE在Nd中通过雷帕霉素复合物1信号通路的靶点上调。然而,作为自噬底物,SQSTM1/p62和泛素化蛋白水平在Nd中升高。此外,BafA1处理对SQSTM1/p62蛋白水平没有影响,表明Nd的自噬通量受损。进一步检测到溶酶体异常酸化,导致成熟CtsL1(组织蛋白酶L1)比例下降。因此,自溶酶体中的底物不能在快速的时间框架内降解,导致蛋白质聚集体的积累,从而导致PSG萎缩和变性。我们还发现,酸性纳米颗粒挽救了溶酶体的酸化,缓解了Nd-PSG的退行性改变。本研究结果表明,Nd突变家蚕可作为研究蛋白质聚集性疾病的动物模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Defective autophagy in a fibroin secretion-deficient silkworm mutant.

The silkworm Bombyx mori is an economically important insect for silk production. Its silk glands are responsible for the synthesis and secretion of silk proteins. The naked pupa (Nd), a fibroin heavy chain mutant strain of silkworm, was found to exhibit severe atrophy, degeneration of the posterior silk gland (PSG), and abnormal secretion of fibroin proteins, thereby producing little or no silk. Here, we found that the autophagic marker Atg8-PE was upregulated through the target of rapamycin complex 1 signaling pathway in Nd. However, as autophagy substrates, SQSTM1/p62 and ubiquitinated protein levels increased in Nd. Furthermore, treatment with BafA1 showed no effect on the protein levels of SQSTM1/p62, indicating impaired autophagic flux in Nd. Abnormal acidification of lysosomes was further detected, which resulted in a decreased proportion of matured CtsL1 (cathepsin L1). Thus, the substrate in autolysosomes cannot be degraded within a rapid time frame, resulting in the accumulation of protein aggregates, which cause atrophy and degeneration of the PSG. We also found that acidic nanoparticles rescued lysosomal acidification and relieved the degenerative changes of Nd-PSG. The findings of this study suggest that the Nd mutant silkworm can be used as an animal model for studying protein aggregation diseases.Abbreviations: AD: Alzheimer disease; aNP: acidic nanoparticle; APP: amyloid beta precursor protein; Atg8: autophagy related 8; BACE1: beta-secretase 1; BafA1: bafilomycin A1; CtsL1: cathepsin L1; CRY: crystallin; ER: endoplasmic reticulum; FibH: fibroin heavy chain; FibL: fibroin light chain; FUS: FUS RNA binding protein; HD: Huntington disease; HRP: horseradish peroxidase; Nd: naked pupa; OSBPL2: oxysterol binding protein like 2; PD: Parkinson disease; PE: phosphatidylethanolamine; p-EIF4EBP: phosphorylated eukaryotic initiation factor 4E binding protein; PROM1: prominin 1; p-RPS6KB: phosphorylated ribosomal protein S6 kinase B; PSEN: presenilin; PSG: posterior silk gland; SDS-PAGE: sodium dodecyl sulfate-polyacrylamide gel electrophoresis; SEM: standard error of the mean; SOD1: superoxide dismutase 1; SQSTM1/p62: sequestosome 1; TARDBP: TAR DNA binding protein; TORC1: target of rapamycin complex 1; UBQLN2: ubiquilin 2; V-ATPase: vacuolar-type ATPase.

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