Opitz-Araya Ximena, Barria Andres
Department of Physiology and Biophysics, University of Washington School of Medicine, USA.
J Vis Exp. 2011 Feb 3(48):2462. doi: 10.3791/2462.
The hippocampus, a component of the limbic system, plays important roles in long-term memory and spatial navigation. Hippocampal neurons can modify the strength of their connections after brief periods of strong activation. This phenomenon, known as long-term potentiation (LTP) can last for hours or days and has become the best candidate mechanism for learning and memory. In addition, the well defined anatomy and connectivity of the hippocampus has made it a classical model system to study synaptic transmission and synaptic plasticity. As our understanding of the physiology of hippocampal synapses grew and molecular players became identified, a need to manipulate synaptic proteins became imperative. Organotypic hippocampal cultures offer the possibility for easy gene manipulation and precise pharmacological intervention but maintain synaptic organization that is critical to understanding synapse function in a more naturalistic context than routine culture dissociated neurons methods. Here we present a method to prepare and culture hippocampal slices that can be easily adapted to other brain regions. This method allows easy access to the slices for genetic manipulation using different approaches like viral infection or biolistics. In addition, slices can be easily recovered for biochemical assays, or transferred to microscopes for imaging or electrophysiological experiments.
海马体是边缘系统的一个组成部分,在长期记忆和空间导航中发挥着重要作用。海马神经元在短暂的强烈激活后能够改变其连接强度。这种被称为长时程增强(LTP)的现象可以持续数小时或数天,并且已成为学习和记忆的最佳候选机制。此外,海马体明确的解剖结构和连接性使其成为研究突触传递和突触可塑性的经典模型系统。随着我们对海马突触生理学的理解不断深入以及分子作用者被确定,操纵突触蛋白变得势在必行。器官型海马培养物提供了易于进行基因操作和精确药理学干预的可能性,同时保持了突触组织,这对于在比常规培养解离神经元方法更自然的背景下理解突触功能至关重要。在这里,我们介绍一种制备和培养海马切片的方法,该方法可以很容易地应用于其他脑区。这种方法允许使用病毒感染或生物弹道学等不同方法轻松获取切片进行基因操作。此外,切片可以很容易地回收用于生化分析,或转移到显微镜下进行成像或电生理实验。