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蛋白磷酸酶 2A 亚基 PPP2R2C 在阿尔茨海默病转基因小鼠的大脑中下调。

PP2A subunit PPP2R2C is downregulated in the brains of Alzheimer's transgenic mice.

机构信息

Shanghai Ruijin Hospital, Shanghai Ruijin Hospital North, Affiliated to Shanghai Jiaotong University School of Medicine, International Laboratory in Hematology, Aging and Cancer, State Key Laboratory of Medical Genomics, Pôle Sino-Français de Recherche en Sciences du Vivant et Génomique, Shanghai, P.R. China.

Shanghai Ruijin Hospital North, Shanghai Jiaotong University School of Medicine, Shanghai, P.R. China.

出版信息

Aging (Albany NY). 2020 Apr 14;12(8):6880-6890. doi: 10.18632/aging.103048.

Abstract

Targeting of PP2A suggests a close link to tau-related cognitive and functional declines. However, little is known about how the expression of PP2A subunits and PP2A activity are dysregulated in the course of AD, precluding any specific targeting strategy for restoring PP2A in AD patients. Although the PP2A heterotrimer containing the regulatory subunit PR55/Bα (encoded by the gene) is the major tau phosphatase, the involvement of other brain-specific PP2A regulatory subunits in tau dephosphorylation remains unknown. PR55/Bγ (encoded by the gene) is a pivotal phosphatase in the brain, and single-nucleotide polymorphisms (SNPs) of are involved in several mental disorders. By measuring the differential spatiotemporal expression patterns of PPP2R2C in Wt and transgenic AD mice, we revealed that PPP2R2C expression is downregulated in the aged AD mouse brain as compared to the Wt mouse brain. In cultured cells, expression regulates PP2A activity and tau dephosphorylation. These results suggest that dysregulation of PPP2R2C expression may be involved in the onset of AD and that specifically targeting PPP2R2C expression or activity is a promising strategy against brain dementia disorders, including AD and other tauopathies.

摘要

靶向 PP2A 提示其与与 Tau 相关的认知和功能下降密切相关。然而,目前对于 AD 进程中 PP2A 亚基的表达和 PP2A 活性如何失调知之甚少,这使得针对 AD 患者恢复 PP2A 活性的靶向治疗策略难以实现。尽管含有调节亚基 PR55/Bα(由 基因编码)的 PP2A 异三聚体是 Tau 的主要磷酸酶,但其他脑特异性 PP2A 调节亚基在 Tau 去磷酸化中的参与情况尚不清楚。PR55/Bγ(由 基因编码)是大脑中的关键磷酸酶, 基因的单核苷酸多态性(SNP)与多种精神障碍有关。通过测量野生型和转基因 AD 小鼠中 PPP2R2C 的差异时空表达模式,我们发现与野生型小鼠大脑相比,PPP2R2C 在老年 AD 小鼠大脑中的表达下调。在培养的细胞中, 表达调节 PP2A 活性和 Tau 去磷酸化。这些结果表明,PPP2R2C 表达的失调可能与 AD 的发病有关,而针对 PPP2R2C 表达或活性的靶向治疗可能是预防包括 AD 和其他 Tau 病在内的脑痴呆疾病的有前途的策略。

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