Cantarutti Kristyn C, Burgess Jason, Brill Julie A, Dason Jeffrey S
a Department of Biological Sciences , University of Windsor , Windsor , Canada.
b Program in Cell Biology , The Hospital for Sick Children , Toronto , Canada.
J Neurogenet. 2018 Sep;32(3):230-235. doi: 10.1080/01677063.2018.1502762. Epub 2018 Sep 3.
Type II phosphatidylinositol 4-kinase (PI4KII) is thought to be associated with synaptic vesicles (SVs) and to be responsible for the majority of PI4K activity in the nervous system. However, the function of PI4KII at the synapse is unknown. We characterized the synaptic phenotypes of a Drosophila melanogaster PI4KII null mutant. We found increased nerve terminal growth in PI4KII null mutants indicating that PI4KII restrains nerve terminal growth. Evoked neurotransmitter release elicited in response to low frequency stimulation and spontaneous neurotransmitter release were not altered in PI4KII null mutants. However, PI4KII null mutants displayed reduced FM1-43 uptake in response to stimulation by high K saline, indicating impaired SV endocytosis. PI4KII null mutants did not display any defects in FM1-43 unloading, consistent with normal SV exocytosis. Thus, PI4KII is required for SV endocytosis but dispensable for SV exocytosis. Overall, our data show that PI4KII regulates both nerve terminal growth and SV recycling.
II型磷脂酰肌醇4激酶(PI4KII)被认为与突触小泡(SVs)相关,并在神经系统中负责大部分PI4K活性。然而,PI4KII在突触处的功能尚不清楚。我们对果蝇PI4KII基因敲除突变体的突触表型进行了表征。我们发现PI4KII基因敲除突变体的神经末梢生长增加,这表明PI4KII抑制神经末梢生长。在PI4KII基因敲除突变体中,低频刺激引发的诱发神经递质释放和自发神经递质释放没有改变。然而,PI4KII基因敲除突变体在高钾盐刺激下的FM1-43摄取减少,表明突触小泡内吞作用受损。PI4KII基因敲除突变体在FM1-43卸载方面没有表现出任何缺陷,这与正常的突触小泡胞吐作用一致。因此,PI4KII是突触小泡内吞作用所必需的,但对突触小泡胞吐作用是可有可无的。总体而言,我们的数据表明PI4KII调节神经末梢生长和突触小泡循环。