Choi Jun-Hyeok, Park Pojeong, Baek Gi-Chul, Sim Su-Eon, Kang SukJae Joshua, Lee Yeseul, Ahn Seo-Hee, Lim Chae-Seok, Lee Yong-Seok, Collingridge Graham L, Kaang Bong-Kiun
Mol Brain. 2014 Nov 6;7:78. doi: 10.1186/s13041-014-0078-6.
Previous studies have shown that a family of phosphoinositide 3-kinases (PI3Ks) plays pivotal roles in the brain; in particular, we previously reported that knockout of the γ isoform of PI3K (PI3Kγ) in mice impaired synaptic plasticity and reduced behavioral flexibility. To further examine the role of PI3Kγ in synaptic plasticity and hippocampus-dependent behavioral tasks we overexpressed p110γ, the catalytic subunit of PI3Kγ, in the hippocampal CA1 region. We found that the overexpression of p110γ impairs NMDA receptor-dependent long-term depression (LTD) and hippocampus-dependent spatial learning in the Morris water maze (MWM) task. In contrast, long-term potentiation (LTP) and contextual fear memory were not affected by p110γ overexpression. These results, together with the previous knockout study, suggest that a critical level of PI3Kγ in the hippocampus is required for successful induction of LTD and normal learning.
先前的研究表明,磷酸肌醇3激酶(PI3K)家族在大脑中发挥着关键作用;特别是,我们之前报道过,小鼠中PI3K的γ亚型(PI3Kγ)敲除会损害突触可塑性并降低行为灵活性。为了进一步研究PI3Kγ在突触可塑性和海马体依赖性行为任务中的作用,我们在海马体CA1区过表达了PI3Kγ的催化亚基p110γ。我们发现,p110γ的过表达会损害NMDA受体依赖性长时程抑制(LTD)以及在莫里斯水迷宫(MWM)任务中与海马体相关的空间学习能力。相比之下,长时程增强(LTP)和情境恐惧记忆不受p110γ过表达的影响。这些结果,连同之前的敲除研究,表明海马体中PI3Kγ的关键水平对于成功诱导LTD和正常学习是必需的。