Department of Human Anatomy, Institute of Medicine and Health, Hebei Medical University, Shijiazhuang, 050017, Hebei, China.
The Key Laboratory of Neural and Vascular Biology, Ministry of Education, Hebei Medical University, Shijiazhuang, 050017, Hebei, China.
Mol Neurobiol. 2024 Nov;61(11):8575-8589. doi: 10.1007/s12035-024-04066-y. Epub 2024 Mar 25.
Alzheimer's disease (AD) is a common age-associated progressive neurodegenerative disorder that is implicated in the aberrant regulation of numerous circular RNAs (circRNAs). Here, we reported that circ-Bptf, a conserved circRNA derived from the Bptf gene, showed an age-dependent decrease in the hippocampus of APP/PS1 mice. Overexpression of circ-Bptf significantly reversed dendritic spine loss and learning and memory impairment in APP/PS1 mice. Moreover, we found that circ-Bptf was predominantly localized to the cytoplasm and upregulated p62 expression by binding to miR-138-5p. Furthermore, the miR-138-5p mimics reversed the decreased expression of p62 induced by the silencing of circ-Bptf. Together, our findings suggested that circ-Bptf ameliorated learning and memory impairments via the miR-138-5p/p62 axis in APP/PS1 mice. It may act as a potential player in AD pathogenesis and therapy.
阿尔茨海默病(AD)是一种常见的与年龄相关的进行性神经退行性疾病,涉及许多环状 RNA(circRNAs)的异常调节。在这里,我们报道了 circ-Bptf,一种源自 Bptf 基因的保守 circRNA,在 APP/PS1 小鼠的海马体中表现出与年龄相关的减少。circ-Bptf 的过表达显著逆转了 APP/PS1 小鼠的树突棘丢失和学习记忆损伤。此外,我们发现 circ-Bptf 主要定位于细胞质,并通过结合 miR-138-5p 上调 p62 的表达。此外,miR-138-5p 模拟物逆转了 circ-Bptf 沉默诱导的 p62 表达降低。总之,我们的研究结果表明,circ-Bptf 通过 APP/PS1 小鼠中的 miR-138-5p/p62 轴改善了学习记忆损伤。它可能是 AD 发病机制和治疗的潜在参与者。