Diabetes Influences the Fusion of Autophagosomes With Lysosomes in SH-SY5Y Cells and Induces Aβ Deposition and Cognitive Dysfunction in STZ-induced Diabetic Rats

التفاصيل البيبلوغرافية
العنوان: Diabetes Influences the Fusion of Autophagosomes With Lysosomes in SH-SY5Y Cells and Induces Aβ Deposition and Cognitive Dysfunction in STZ-induced Diabetic Rats
المؤلفون: Lou-Yan Ma, Song-fang Liu, Ya-gang Guo, Zheng-quan Ma, Ya Li, Shu-jin Wang, Yu Niu, Mo Li, Jia-jia Zhai, Su-hang Shang, Ya-Li Lv, Qiu-Min Qu
المصدر: Behavioural brain research.
سنة النشر: 2022
مصطلحات موضوعية: Behavioral Neuroscience, History, Polymers and Plastics, Business and International Management, Industrial and Manufacturing Engineering
الوصف: Diabetes has been regarded as an independent risk factor for Alzheimer's disease (AD). Our previous study found that diabetes activated autophagy, but lysosome function was impaired. Autophagy-lysosome dysfunction may be involved in Aβ deposition in diabetic cognitive impairment. In the present study, we used STZ-induced diabetic rats and SH-SY5Y cells to investigate whether diabetes inhibits autophagosome fusion with lysosomes. We found that in the in vivo study, STZ-induced diabetic rats exhibited cognitive dysfunction, and the lysosome function-related factors CTSL, CTSD, and Rab7 were decreased (P0.05). In an in vitro study, the mRFP-GFP-LC3 assay showed that the fusion of autophagosomes with lysosomes was partly blocked in SH-SY5Y cells. High glucose treatment downregulated the number of autophagolysosomes, downregulated CTSD, CTSL, and Rab7 expression (P0.05), and then influenced the function of ACP2 to partly block the fusion of autophagosomes and lysosomes to inhibit Aβ clearance. These findings indicate that high glucose treatment affected lysosome function, interfered with the fusion of autophagosomes with lysosomes, and partly blocked autophagic flux to influence Aβ clearance.
تدمد: 1872-7549
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b951cf84296c84ecb2e344bfda56f5f
https://pubmed.ncbi.nlm.nih.gov/36610548
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....3b951cf84296c84ecb2e344bfda56f5f
قاعدة البيانات: OpenAIRE