Cheng Hui-Hsuan, Huang Zu-Han, Lin Wei-Hsiang, Chow Wei-Yuan, Chang Yen-Chung
Institute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
J Neurosci Res. 2009 Feb;87(2):460-9. doi: 10.1002/jnr.21852.
Dendritic spines are small protrusions on neuronal dendrites and the major target of the excitatory inputs in mammalian brains. Cultured neurons and brain slices are important tools in studying the biochemical and cellular properties of dendritic spines. During the processes of immunocytochemical studies of neurons and the preparation of brain slices, neurons were often kept at temperatures lower than 37 degrees C for varied lengths of time. This study sought to investigate whether and how cold treatment would affect the protein composition of dendritic spines. The results indicated that upon cold treatment four postsynaptic proteins, namely, alpha,beta-tubulins, calcium, calmodulin-dependent protein kinase IIalpha, and cytoplasmic dynein heavy chain and microtubule-associated protein 2, but not PSD-95 or AMPA receptors, exited from the majority of dendritic spines of cultured rat hippocampal neurons in a Gd(3+)-sensitive manner. The cold-induced exit of tubulins from dendritic spines was further found to be an energy-dependent process involving the activation of Gd(3+)-sensitive calcium channels and ryanodine receptors. The results thus indicate that changes in temperature, calcium concentration, and energy supply of the medium surrounding neurons would affect the protein composition of the dendritic spines and conceivably the protein composition of the subcellular organizations, such as the postsynaptic density, in the cytoplasm of dendritic spines.
树突棘是神经元树突上的小突起,是哺乳动物大脑中兴奋性输入的主要靶点。培养的神经元和脑片是研究树突棘生化和细胞特性的重要工具。在对神经元进行免疫细胞化学研究和制备脑片的过程中,神经元常常在低于37摄氏度的温度下保持不同时长。本研究旨在探究冷处理是否以及如何影响树突棘的蛋白质组成。结果表明,冷处理后,四种突触后蛋白,即α、β微管蛋白、钙/钙调蛋白依赖性蛋白激酶IIα、胞质动力蛋白重链和微管相关蛋白2,但不包括PSD - 95或AMPA受体,以对钆(Gd(3+))敏感的方式从培养的大鼠海马神经元的大多数树突棘中消失。进一步发现,微管蛋白从树突棘的冷诱导消失是一个能量依赖过程,涉及对钆(Gd(3+))敏感的钙通道和雷诺丁受体的激活。因此,结果表明神经元周围培养基的温度、钙浓度和能量供应的变化会影响树突棘的蛋白质组成,并可能影响树突棘细胞质中亚细胞结构(如突触后致密物)的蛋白质组成。