Cousin Michael A, Malladi Chandra S, Tan Timothy C, Raymond Clarke R, Smillie Karen J, Robinson Phillip J
Cell Signalling Unit, Children's Medical Research Institute, Locked Bag 23, Wentworthville 2145, NSW, Australia.
J Biol Chem. 2003 Aug 1;278(31):29065-71. doi: 10.1074/jbc.M302386200. Epub 2003 May 16.
Maintaining synaptic transmission requires replenishment of docked synaptic vesicles within the readily releasable pool (RRP) from synaptic vesicle clusters in the synapsin-bound reserve pool. We show that synapsin forms a complex with phosphatidylinositol 3-kinase (PI 3-kinase) in intact nerve terminals and that synapsin-associated kinase activity increases on depolarization. Disruption of either PI 3-kinase activity or its interaction with synapsin inhibited replenishment of the RRP, but did not affect exocytosis from the RRP. Thus we conclude that a synapsin-associated PI 3-kinase activity plays a role in synaptic vesicle delivery to the RRP. This also suggests that PI 3-kinase contributes to the maintenance of synaptic transmission during periods of high activity, indicating a possible role in synaptic plasticity.
维持突触传递需要从突触结合蛋白结合的储备池中补充易释放池(RRP)内停靠的突触小泡。我们发现,在完整的神经末梢中,突触结合蛋白与磷脂酰肌醇3激酶(PI 3激酶)形成复合物,并且突触结合蛋白相关激酶活性在去极化时增加。PI 3激酶活性的破坏或其与突触结合蛋白的相互作用的破坏均抑制了RRP的补充,但不影响RRP的胞吐作用。因此,我们得出结论,突触结合蛋白相关的PI 3激酶活性在突触小泡向RRP的递送中起作用。这也表明PI 3激酶在高活性期间有助于维持突触传递,表明其在突触可塑性中可能发挥作用。