Department of Anatomy and Cell Biology, University of Kansas Medical School Kansas City, KS, USA.
Front Mol Neurosci. 2012 Feb 15;5:12. doi: 10.3389/fnmol.2012.00012. eCollection 2012.
Neural circuits transmit information through synapses, and the efficiency of synaptic transmission is closely related to the density of presynaptic active zones, where synaptic vesicles are released. The goal of this review is to highlight recent insights into the molecular mechanisms that control the number of active zones per presynaptic terminal (active zone density) during developmental and stimulus-dependent changes in synaptic efficacy. At the neuromuscular junctions (NMJs), the active zone density is preserved across species, remains constant during development, and is the same between synapses with different activities. However, the NMJ active zones are not always stable, as exemplified by the change in active zone density during acute experimental manipulation or as a result of aging. Therefore, a mechanism must exist to maintain its density. In the central nervous system (CNS), active zones have restricted maximal size, exist in multiple numbers in larger presynaptic terminals, and maintain a constant density during development. These findings suggest that active zone density in the CNS is also controlled. However, in contrast to the NMJ, active zone density in the CNS can also be increased, as observed in hippocampal synapses in response to synaptic plasticity. Although the numbers of known active zone proteins and protein interactions have increased, less is known about the mechanism that controls the number or spacing of active zones. The following molecules are known to control active zone density and will be discussed herein: extracellular matrix laminins and voltage-dependent calcium channels, amyloid precursor proteins, the small GTPase Rab3, an endocytosis mechanism including synaptojanin, cytoskeleton protein spectrins and β-adducin, and a presynaptic web including spectrins. The molecular mechanisms that organize the active zone density are just beginning to be elucidated.
神经回路通过突触传递信息,突触传递的效率与突触前活跃区(即突触小泡释放的部位)的密度密切相关。本综述的目的是强调最近在控制突触效能发育和刺激依赖性变化过程中每个突触前末梢(活跃区密度)的活跃区数量的分子机制方面的新见解。在神经肌肉接头(NMJs)中,活跃区密度在不同物种间保持不变,在发育过程中保持不变,并且在具有不同活性的突触之间保持不变。然而,NMJ 的活跃区并不总是稳定的,例如在急性实验操作过程中或随着年龄的增长,活跃区密度会发生变化。因此,必须存在一种机制来维持其密度。在中枢神经系统(CNS)中,活跃区的大小受到限制,在较大的突触前末梢中存在多个活跃区,并且在发育过程中保持密度不变。这些发现表明,CNS 中的活跃区密度也受到控制。然而,与 NMJ 不同的是,CNS 中的活跃区密度也可以增加,如在海马突触中观察到的对突触可塑性的反应。尽管已知的活跃区蛋白和蛋白相互作用的数量有所增加,但对于控制活跃区数量或间隔的机制知之甚少。以下分子被认为可以控制活跃区的密度,将在本文中进行讨论:细胞外基质层粘连蛋白和电压依赖性钙通道、淀粉样前体蛋白、小 GTP 酶 Rab3、包括突触结合蛋白在内的内吞作用机制、细胞骨架蛋白 spectrins 和 β-辅肌动蛋白以及包括 spectrins 在内的突触前网。组织活跃区密度的分子机制才刚刚开始被阐明。