Institute of Biochemical Sciences, College of Life Science, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei, 10617, Taiwan.
Graduate Institute of Anatomy and Cell Biology, National Taiwan University, Taipei, Taiwan.
Sci Rep. 2020 Jul 2;10(1):10857. doi: 10.1038/s41598-020-67675-2.
PHRF1 is involved in transforming growth factor β (TGF-β) signaling to constrain the formation of acute promyelocytic leukemia (APL) in mouse APL models. PHRF1 also participates in modulating non-homologous end-joining. However, the role of PHRF1 in mammalian dendrite architecture and synaptic plasticity is unclear. Here, we investigated the role of PHRF1 in dendritic formation in the murine hippocampus using Camk2a promoter driven-iCre recombinase to conduct a PHRF1 conditional knockout, namely PHRF1, in the forebrain region. PHRF1 mice developed normally, but exhibited anxiety-like behaviors and displayed defective spatial memory. Alterations of dendritic complexity in apical and basal dendrites of pyramidal neurons were noticed in PHRF1 mutants. Furthermore, electrical stimulation in the hippocampal CA1 region after the TGF-β1 treatment showed a reduced synaptic plasticity in PHRF1 mice. Immunoblotting analysis indicated that PHRF1 ablation affected the TGF-β signaling. Collectively, our results demonstrate that PHRF1 is important for the dendritic architecture and required for spatial memory formation in the hippocampus.
PHRF1 参与转化生长因子 β(TGF-β)信号转导,以限制急性早幼粒细胞白血病(APL)在小鼠 APL 模型中的形成。PHRF1 还参与调节非同源末端连接。然而,PHRF1 在哺乳动物树突结构和突触可塑性中的作用尚不清楚。在这里,我们使用 Camk2a 启动子驱动的-iCre 重组酶研究了 PHRF1 在小鼠海马体树突形成中的作用,以在前脑区域进行 PHRF1 的条件性敲除,即 PHRF1。PHRF1 小鼠正常发育,但表现出焦虑样行为,并表现出空间记忆缺陷。在 PHRF1 突变体中注意到锥体神经元的顶树突和基底树突的复杂性发生改变。此外,在 TGF-β1 处理后海马 CA1 区进行电刺激显示 PHRF1 小鼠的突触可塑性降低。免疫印迹分析表明,PHRF1 缺失会影响 TGF-β 信号。总之,我们的结果表明 PHRF1 对于树突结构很重要,并且对于海马体中的空间记忆形成是必需的。