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作 者:袁方 巫祖君 龙振宇 毕丹蕾 申勇 YUAN Fang;WU Zu-Jun;LONG Zhen-Yu;BI Dan-Lei;SHEN Yong(Institute on Aging and Brain Disorders,The First Affiliated Hospital of USTC,School of Life Science,Division of Life Science and Medicine,University of Science and Technology of China,Hefei 230026,China;Neurodegenerative Disorder Research Center,CAS Key Laboratory of Brain Function and Disease,University of Science and Technology of China,Hefei 230026,China;Center for Excellence in Brain Science and Intelligence Technology,Chinese Academy of Sciences,Shanghai 200031,China)
机构地区:[1]中国科学技术大学生命科学与医学部生命科学学院,中国科学技术大学第一附属医院脑衰老与脑疾病研究中心,合肥230026 [2]中国科学技术大学中国科学院脑功能与脑疾病重点实验室,中国科学技术大学神经退行性疾病研究中心,合肥230026 [3]中国科学院脑科学与智能技术卓越创新中心,上海200031
出 处:《生物化学与生物物理进展》2023年第1期135-144,共10页Progress In Biochemistry and Biophysics
基 金:国家自然科学基金(32100796,91749209),中央高校基本科研业务费专项资金(WK9100000011)和国家科技攻关计划(2021YFA0804900,2016YFC1300500-3)资助项目。
摘 要:目的β分泌酶1(BACE1)是阿尔茨海默病患者脑中淀粉样蛋白(Aβ)产生的关键酶。肌养蛋白聚糖(dystroglycan,DG)帮助星形胶质细胞的终足锚定在脑血管上,形成一道支持血脑屏障的胶质界限。一项无靶标蛋白质组学研究指出BACE1可能会下调DG的表达水平。本文旨在研究BACE1能否调控DG的蛋白质水平及其可能的调控机制。方法利用瞬时转染法在HEK-293T细胞系和原代培养的小鼠星形胶质细胞中表达目的蛋白。通过蛋白质免疫印迹分析目标蛋白质的相对水平。利用基因荧光定量和免疫共沉淀技术探索BACE1调控DG的潜在机制。结果在HEK-293T和原代小鼠星形胶质细胞中引入BACE1会使DGβ亚基(β-DG)的蛋白质水平显著降低。在HEK-293T细胞中,β-DG蛋白水平的下降依赖于BACE1的酶活性。结论在HEK-293T细胞和小鼠星形胶质细胞中,BACE1使β-DG的蛋白质水平下降。Objective Beta-secretase 1(BACE1) is the key enzyme for amyloid β(Aβ) production in the Alzheimer’ s disease(AD) brain. The dystroglycan(DG) protein anchors astroglial endfeet onto cerebral blood vessels forming glia limitans, a supportive element in the blood-brain barrier. An untargeted proteomics study predicted that BACE1 downregulates DG expression. Here, this study investigated whether BACE1 modulates the protein levels of DG and its hypothetic mechanism. Methods Transient transfection technique was used to express target protein in HEK-293T cells and in primary mouse astrocytes. And the protein levels of targets were analyzed by Western blot. Quantitative polymerase chain reaction and co-immunoprecipitation were used to explore the potential mechanisms of BACE1-dependent regulation of DG. Results This study found that addition of BACE1 resulted in significantly lower levels of β subunit DG(β-DG) protein, both in HEK-293T cells and in primary mouse astrocytes. And in HEK-293T cells, this down-regulation of β-DG protein dependent on the enzyme activity of BACE1. Conclusion BACE1 lowers β-DG protein levels in HEK-293T cells and in mouse astrocytes.
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