Dept. of Pharmacology, Univ. of Minnesota, 6-120 Jackson Hall, 321 Church St. SE, Minneapolis, MN 55455, USA.
J Neurophysiol. 2013 Mar;109(6):1494-504. doi: 10.1152/jn.00580.2012. Epub 2012 Dec 28.
Neurons adapt to seizure activity structurally and functionally to attenuate hyperactive neural circuits. Homer proteins provide a scaffold in the postsynaptic density (PSD) by binding to ligands through an EVH1 domain and to other Homer proteins by a coiled-coil domain. The short Homer isoform 1a (H1a) has a ligand-binding domain but lacks a coiled-coil domain and thus acts in a dominant-negative manner to uncouple Homer scaffolds. Here, we show that treating rat hippocampal cultures with bicuculline and 4-aminopyridine (Bic+4-AP) evoked epileptiform activity and synchronized Ca(2+) spiking, measured with whole cell current-clamp and fura-2-based digital imaging; Bic+4-AP increased H1a mRNA through the activation of metabotropic glutamate receptor 5 (mGluR5). Treatment with Bic+4-AP for 4 h attenuated burst firing and induced synapse loss. Synaptic changes were measured using a confocal imaging-based assay that quantified clusters of PSD-95 fused to green fluorescent protein. Treatment with an mGluR5 antagonist blocked H1a expression, synapse loss, and burst attenuation. Overexpression of H1a inhibited burst firing similar to Bic+4-AP treatment. Furthermore, knockdown of H1a using a short hairpin RNA (shRNA) strategy reduced synapse loss and burst attenuation induced by Bic+4-AP treatment. Thus an epileptiform stimulus applied to hippocampal neurons in culture induced burst firing and H1a expression through the activation of mGluR5; a 4-h exposure to this stimulus resulted in synapse loss and burst attenuation. These results suggest that H1a expression functions in a negative-feedback manner to reduce network excitability by regulating the number of synapses.
神经元通过结构和功能适应癫痫活动,从而减弱过度活跃的神经回路。 Homer 蛋白通过 EVH1 结构域与配体结合,并通过卷曲螺旋结构域与其他 Homer 蛋白结合,在突触后密度 (PSD) 中提供支架。短 Homer 同种型 1a (H1a) 具有配体结合结构域,但缺乏卷曲螺旋结构域,因此以显性负性方式发挥作用,使 Homer 支架解偶联。在这里,我们表明,用 Bicuculline 和 4-氨基吡啶 (Bic+4-AP) 处理大鼠海马培养物可引发癫痫样活动和同步 Ca(2+) 爆发,通过全细胞膜电流钳和基于 fura-2 的数字成像进行测量;Bic+4-AP 通过激活代谢型谷氨酸受体 5 (mGluR5) 增加 H1a mRNA。用 Bic+4-AP 处理 4 小时可减弱爆发性放电并诱导突触丢失。使用基于共聚焦成像的测定法测量突触变化,该测定法定量了融合 GFP 的 PSD-95 簇。用 mGluR5 拮抗剂处理可阻断 H1a 表达、突触丢失和爆发衰减。H1a 的过表达类似于 Bic+4-AP 处理抑制爆发性放电。此外,使用短发夹 RNA (shRNA) 策略敲低 H1a 可减少 Bic+4-AP 处理引起的突触丢失和爆发衰减。因此,培养的海马神经元中的癫痫样刺激通过激活 mGluR5 诱导爆发性放电和 H1a 表达;4 小时暴露于这种刺激会导致突触丢失和爆发衰减。这些结果表明,H1a 表达通过调节突触数量以负反馈方式发挥作用,从而降低网络兴奋性。