Bellani Serena, Sousa Vitor L, Ronzitti Giuseppe, Valtorta Flavia, Meldolesi Jacopo, Chieregatti Evelina
Commun Integr Biol. 2010 Mar;3(2):106-9. doi: 10.4161/cib.3.2.10964.
The cytosolic protein alpha-synuclein is enriched at the pre-synaptic terminals of almost all types of neurons in the central nervous system. alpha-Synuclein overexpression and the expression of three different mutants have been shown to sustain the pathogenesis of selected forms of Parkinson's disease. The localization of the protein and the defects found in knocked out or transgenic animals suggest a role of alpha-synuclein in the regulation of synaptic efficiency. However, the precise function of the protein and the molecular mechanisms of its action are still unclear. At synapses the synaptic vesicle release cycle is a finely tuned process composed of sequential steps that require the interconnected participation of several proteins and cytoskeletal elements. Actin microfilaments are required for the regulation of synaptic vesicle mobilization between different functional pools, for their organization at the active zone and influence the exocytotic process. We recently identified actin as a possible target of alpha-synuclein function. Through its binding to actin and the regulation of actin dynamics, alpha-synuclein could participate in the tuning of the vesicle release process, thereby modulating synaptic function and plasticity.
胞质蛋白α-突触核蛋白在中枢神经系统几乎所有类型神经元的突触前终末中含量丰富。α-突触核蛋白的过表达以及三种不同突变体的表达已被证明与某些形式帕金森病的发病机制有关。该蛋白的定位以及在基因敲除或转基因动物中发现的缺陷表明α-突触核蛋白在调节突触效率中发挥作用。然而,该蛋白的确切功能及其作用的分子机制仍不清楚。在突触处,突触小泡释放周期是一个精细调节的过程,由一系列步骤组成,这些步骤需要多种蛋白质和细胞骨架成分的相互参与。肌动蛋白微丝对于调节突触小泡在不同功能池之间的移动、在活性区的组织以及影响胞吐过程是必需的。我们最近确定肌动蛋白是α-突触核蛋白功能的一个可能靶点。通过与肌动蛋白结合并调节肌动蛋白动力学,α-突触核蛋白可能参与小泡释放过程的调节,从而调节突触功能和可塑性。