Schnell E, Nicoll R A
Department of Cellular and Molecular Pharmacology, University of California, San Francisco, California 94143, USA.
J Neurophysiol. 2001 Apr;85(4):1498-501. doi: 10.1152/jn.2001.85.4.1498.
Recent studies have identified myosin Va as an organelle motor that may have important functions in neurons. Abundantly expressed at the hippocampal postsynaptic density, it interacts with protein complexes involved in synaptic plasticity. It is also located in presynaptic terminals and may function to recruit vesicles in the reserve pool to the active zone. Dilute-lethal mice are spontaneous myosin Va mutants and have severe neurological symptoms. We studied hippocampal physiology at CA3-CA1 excitatory synapses in dilute-lethal mutant mice to test the hypothesis that myosin Va plays a role in pre- or postsynaptic elements of synaptic transmission. In all assays performed, the mutant synapses appeared to be functioning normally, both pre- and postsynaptically. These data suggest that myosin Va is not essential for the synaptic release machinery, postsynaptic receptor composition, or plasticity at this synapse, but does not exclude significant roles for myosin Va in other cell types nor potential compensation by other myosin V isoforms.
最近的研究已确定肌球蛋白Va是一种细胞器马达,可能在神经元中具有重要功能。它在海马突触后致密区大量表达,与参与突触可塑性的蛋白质复合物相互作用。它也位于突触前终末,可能起到将储备池中的囊泡募集到活性区的作用。稀释致死小鼠是自发的肌球蛋白Va突变体,具有严重的神经症状。我们研究了稀释致死突变小鼠CA3-CA1兴奋性突触处的海马生理学,以检验肌球蛋白Va在突触传递的突触前或突触后元件中发挥作用的假设。在所有进行的实验中,突变突触在突触前和突触后似乎都正常发挥功能。这些数据表明,肌球蛋白Va对于该突触的突触释放机制、突触后受体组成或可塑性并非必不可少,但并不排除肌球蛋白Va在其他细胞类型中发挥重要作用,也不排除其他肌球蛋白V亚型的潜在补偿作用。