Fifková E
Cell Mol Neurobiol. 1985 Jun;5(1-2):47-63. doi: 10.1007/BF00711085.
A number of experimental procedures which induce increased electrical activity (including long-term potentiation) were shown to be accompanied by morphometric changes in dendritic spines. These changes include an enlargement of the spine head, shortening and widening of the spine stalk, and an increase in the length of synaptic apposition. A possible mechanism is suggested which takes into account specific cytological features of the spine and the existence of contractile proteins in neurons. Dendritic spines are defined as special domains of the neuron which have a unique organization of the cytoplasm. Actin filaments form a very dense network in the spine head, and they are longitudinally organized within the spine stalk. Spines were also shown to contain myosin and other actin-regulatory proteins. The high density of the actin network could explain the characteristic absence of the cytoplasmic organelles from dendritic spines. In analogy with other cells, such an actin organization indicates low levels of free cytosolic calcium. Even in the resting state, calcium levels may be unevenly distributed through the neuron, being lowest within the subplasmalemmal region. Due to the high surface-to-volume ratio in spines, the cytoplasm is formed mostly by the subplasmalemmal region. The spine apparatus or the smooth endoplasmic reticulum, which is recognized as a calcium-sequestering site in spines, may also contribute to the low calcium levels there. However, when in the stimulated spine the voltage-dependent calcium channels open, then, given the spine's high surface-to-volume ratio, the concentration of calcium may very quickly attain levels that will activate the actin-regulatory proteins and myosin and thus trigger the chain of events leading to the enlargement of the spine head and to the contraction (i.e., widening and shortening) of the spine stalk. The increased free cytosolic calcium may also activate the protein-producing system localized at the base of the spine, which, under certain conditions, could stabilize the morphometric changes of the spine.
许多能诱导电活动增强(包括长时程增强)的实验程序都显示伴随着树突棘的形态计量学变化。这些变化包括棘头增大、棘柄缩短变宽以及突触附着长度增加。文中提出了一种可能的机制,该机制考虑到了棘的特定细胞学特征以及神经元中收缩蛋白的存在。树突棘被定义为神经元具有独特细胞质组织的特殊区域。肌动蛋白丝在棘头中形成非常密集的网络,并且它们在棘柄内纵向排列。研究还表明棘中含有肌球蛋白和其他肌动蛋白调节蛋白。肌动蛋白网络的高密度可以解释树突棘中细胞质细胞器缺失的特征。与其他细胞类似,这种肌动蛋白组织表明游离胞质钙水平较低。即使在静息状态下,钙水平在神经元内的分布也可能不均匀,在质膜下区域最低。由于棘中高的表面积与体积比,细胞质主要由质膜下区域形成。棘器或光滑内质网,被认为是棘中钙的储存位点,也可能导致那里的低钙水平。然而,当受刺激的棘中电压依赖性钙通道打开时,鉴于棘的高表面积与体积比,钙浓度可能很快达到激活肌动蛋白调节蛋白和肌球蛋白的水平,从而触发导致棘头增大和棘柄收缩(即变宽和缩短)的一系列事件。增加的游离胞质钙也可能激活位于棘基部的蛋白质产生系统,在某些条件下,该系统可以稳定棘的形态计量学变化。