Quantitative and Systems Biology Graduate Program, University of California, Merced, CA 95343, USA.
Molecular Cell Biology, School of Natural Sciences, University of California, Merced, CA 95343, USA.
Cell Rep. 2018 Feb 13;22(7):1647-1656. doi: 10.1016/j.celrep.2018.01.049.
Ethanol is the most common drug of abuse. It exerts its behavioral effects by acting on widespread neural circuits; however, its impact on glial cells is less understood. We show that Drosophila perineurial glia are critical for ethanol tolerance, a simple form of behavioral plasticity. The perineurial glia form the continuous outer cellular layer of the blood-brain barrier and are the interface between the brain and the circulation. Ethanol tolerance development requires the A kinase anchoring protein Akap200 specifically in perineurial glia. Akap200 tightly coordinates protein kinase A, actin, and calcium signaling at the membrane to control tolerance. Furthermore, ethanol causes a structural remodeling of the actin cytoskeleton and perineurial membrane topology in an Akap200-dependent manner, without disrupting classical barrier functions. Our findings reveal an active molecular signaling process in the cells at the blood-brain interface that permits a form of behavioral plasticity induced by ethanol.
乙醇是最常见的滥用药物。它通过作用于广泛的神经回路来发挥其行为效应;然而,其对神经胶质细胞的影响还不太清楚。我们表明,果蝇周细胞神经胶质细胞对乙醇耐受至关重要,这是一种简单的行为可塑性形式。周细胞神经胶质细胞形成血脑屏障的连续外细胞层,是大脑和循环之间的界面。乙醇耐受的发展需要 A 激酶锚定蛋白 Akap200 专门在周细胞神经胶质细胞中。Akap200 紧密协调蛋白激酶 A、肌动蛋白和钙信号在膜上,以控制耐受。此外,乙醇以依赖于 Akap200 的方式引起肌动蛋白细胞骨架和周细胞膜拓扑结构的结构重塑,而不会破坏经典的屏障功能。我们的发现揭示了血脑界面细胞中的一个活跃的分子信号过程,该过程允许乙醇诱导的行为可塑性形式。