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The effect of BACE1-AS on β-amyloid generation by regulating BACE1 mRNA expression

BACKGROUND: The BACE1 antisense transcript (BACE1-AS) is a conserved long noncoding RNA (lncRNA). The level of BACE1-AS is significantly increased and the level of the BACE1 mRNA is slightly increased in subjects with AD. BACE1-AS exerts a significant moderating effect on the expression of the BACE1...

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Detalles Bibliográficos
Autores principales: Li, Fan, Wang, Yun, Yang, Hui, Xu, Yingying, Zhou, Xiaoyan, Zhang, Xiao, Xie, Zhaohong, Bi, Jianzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771094/
https://www.ncbi.nlm.nih.gov/pubmed/31570097
http://dx.doi.org/10.1186/s12867-019-0140-0
Descripción
Sumario:BACKGROUND: The BACE1 antisense transcript (BACE1-AS) is a conserved long noncoding RNA (lncRNA). The level of BACE1-AS is significantly increased and the level of the BACE1 mRNA is slightly increased in subjects with AD. BACE1-AS exerts a significant moderating effect on the expression of the BACE1 mRNA and promotes the formation of Aβ. After the administration of Aβ(1-42) to SH-SY5Y cells and C57/BL6J mice, we detected the expression of BACE1-AS, BACE1 mRNA, and BACE1 protein, as well as the concentration of Aβ(1-40). Then, we silenced the expression of BACE1-AS in SH-SY5Y and 20E2 cells using siRNAs targeting BACE1-AS and detected its effects on the levels of the BACE1 mRNA and BACE1 protein and Aβ(1-40) generation. RESULTS: The administration of Aβ(1-42) increased the expression of BACE1-AS, BACE1 mRNA and protein, as well as the concentration of Aβ(1-40) in SH-SY5Y cells and the brains of C57BL/6J mice. Pretreatment with the BACE1-AS siRNA inhibited the effect of Aβ(1-42) on increasing the expression of BACE1-AS and BACE1, as well as the generation of Aβ. CONCLUSIONS: The mechanism by which exogenous Aβ(1-42) induces BACE1 expression and Aβ generation is mediated by BACE1-AS. BACE1-AS is involved in the mechanism regulating BACE1 expression and Aβ generation in APPsw transgenic cells.