Distinct Functions of Endophilin Isoforms in Synaptic Vesicle Endocytosis. (22nd November 2015)

• Record Type: Journal Article
• Authors: Zhang, Jifeng; Tan, Minghui; Yin, Yichen; Ren, Bingyu; Jiang, Nannan; Guo, Guoqing; Chen, Yuan
• Other Names: Munoz Pablo Academic Editor.
• Is Part Of: Neural plasticity. Volume 2015(2015)
• Publication Date: 2015-11-22
• Subjects: Neuroplasticity -- Periodicals; 612.82
• DOI: 10.1155/2015/371496
• Languages: English
• ISSNs: 2090-5904

Abstract

Abstract : Endophilin isoforms perform distinct characteristics in their interactions with N-type Ca 2+ channels and dynamin. However, precise functional differences for the endophilin isoforms on synaptic vesicle (SV) endocytosis remain unknown. By coupling RNA interference and electrophysiological recording techniques in cultured rat hippocampal neurons, we investigated the functional differences of three isoforms of endophilin in SV endocytosis. The results showed that the amplitude of normalized evoked excitatory postsynaptic currents in endophilin1 knockdown neurons decreased significantly for both single train and multiple train stimulations. Similar results were found using endophilin2 knockdown neurons, whereas endophilin3 siRNA exhibited no change compared with control neurons. Endophilin1 and endophilin2 affected SV endocytosis, but the effect of endophilin1 and endophilin2 double knockdown was not different from that of either knockdown alone. This result suggested that endophilin1 and endophilin2 functioned together but not independently during SV endocytosis. Taken together, our results indicate that SV endocytosis is sustained by endophilin1 and endophilin2 isoforms, but not by endophilin3, in primary cultured hippocampal neurons.