Department of Neurobiology, George S. Wise Faculty of Life Sciences, Tel-Aviv University, Tel-Aviv, Israel.
PLoS One. 2011 Apr 12;6(4):e18579. doi: 10.1371/journal.pone.0018579.
The three neurexins genes (NRXN1/2/3) encode polymorphic synaptic membrane proteins that are involved in cognitive functioning. Neurexins' selectivity of function is presumably conferred through differential use of 2 promoters and 5 alternative splicing sites (SS#1/2/3/4/5). In day-old rat brain neurons grown in culture, activation (depolarization) induces reversible, calcium dependent, repression of NRXN2α SS#3 insert. The effects of depolarization on NRXN1/2/3α splicing and biochemical pathways mediating them were further studied in these neurons. NRXN1/2/3α splicing in the course of memory formation in vivo was also explored, using fear conditioning paradigm in rats in which the animals were trained to associate an aversive stimulus (electrical shock) with a neutral context (a tone), resulting in the expression of fear responses to the neutral context.In the cultured neurons depolarization induced, beside NRXN2α SS#3, repression of SS#3 and SS#4 exons in NRXN3α but not NRXN1α. The repressions were mediated by the calcium/protein kinase C/Rho-associated protein kinase (ROCK) pathway. Fear conditioning induced significant and transient repressions of the NRXN1/2/3α SS#4 exons in the rat hippocampus. ROCK inhibition prior to training attenuated the behavioral fear response, the NRXN1/2/3α splicing repressions and subsequent recovery and the levels of excitatory (PSD95) and inhibitory (gephyrin) synaptic proteins in the hippocampus. No such effects were observed in the prefrontal cortex. Significant correlations existed between the fear response and hippocampal NRXN3α and NRXN2α SS#4 inserts as well as PSD95 protein levels. Hippocampal NRXN1α SS#4 insert and gephyrin levels did not correlate with the behavioral response but were negatively correlated with each other.These results show for the first time dynamic, experience related changes in NRXN1/2/3α alternative splicing in the rat brain and a role for ROCK in them. Specific neurexins' transcripts may be involved in synaptic remodeling occurring at an intermediate (hours) time scale in the course of memory formation.
三个神经连接蛋白基因(NRXN1/2/3)编码多态性突触膜蛋白,参与认知功能。神经连接蛋白的功能选择性可能是通过差异使用 2 个启动子和 5 个选择性剪接位点(SS#1/2/3/4/5)实现的。在培养的新生大鼠脑神经元中,激活(去极化)诱导 NRXN2α SS#3 插入的可逆、钙依赖性抑制。进一步研究了这些神经元中去极化对 NRXN1/2/3α 剪接和介导它们的生化途径的影响。还使用大鼠恐惧条件反射范式探索了体内记忆形成过程中 NRXN1/2/3α 的剪接,其中动物被训练将厌恶刺激(电击)与中性环境(音调)联系起来,导致对中性环境的恐惧反应。在培养的神经元中,去极化诱导了除 NRXN2α SS#3 之外,NRXN3α 的 SS#3 和 SS#4 外显子的抑制,但 NRXN1α 没有。这些抑制是由钙/蛋白激酶 C/ Rho 相关蛋白激酶(ROCK)途径介导的。恐惧条件反射诱导大鼠海马 NRXN1/2/3α SS#4 外显子的显著和短暂抑制。训练前抑制 ROCK 减弱了行为恐惧反应、NRXN1/2/3α 剪接抑制以及随后的恢复以及海马中的兴奋性(PSD95)和抑制性(gephyrin)突触蛋白的水平。在前额叶皮层中没有观察到这种效应。恐惧反应与海马 NRXN3α 和 NRXN2α SS#4 插入物以及 PSD95 蛋白水平之间存在显著相关性。海马 NRXN1α SS#4 插入物和 gephyrin 水平与行为反应无关,但彼此呈负相关。这些结果首次显示了大鼠大脑中 NRXN1/2/3α 选择性剪接的动态、与经验相关的变化,以及 ROCK 在其中的作用。特定的神经连接蛋白转录本可能参与记忆形成过程中中间(小时)时间尺度上发生的突触重塑。