Simultaneous monitoring of three key neuronal functions in primary neuronal cultures.

Abstract:

:The coupling of Ca(2+) influx to synaptic vesicle (SV) recycling in nerve terminals is essential for neurotransmitter release and thus neuronal communication. Both of these parameters have been monitored using fluorescent reporter dyes such as fura-2 and FM1-43 in single central nerve terminals. However, their simultaneous monitoring has been hampered by the proximity of their fluorescence spectra, resulting in significant contamination of their signals by bleedthrough. We have developed an assay that simultaneously monitors both SV recycling and changes in intracellular free Ca(2+) ([Ca(2+)](i)) in cultured neurons using the reporter dyes FM4-64 and fura-2AM. By monitoring both fura-2 and FM4-64 emission in the far red range, we were able to visualize functionally independent readouts of both SV recycling and [Ca(2+)](i) independent of fluorescence bleedthrough. We were also able to incorporate an assay of cell viability without any fluorescence bleedthrough from either fura-2 or FM4-64 signals, using the dye SYTOX Green. We propose that this assay of three key neuronal functions could be simply translated into a high content screening format for studies investigating small molecule inhibitors of these processes.

journal_name

J Neurosci Methods

authors

Evans GJ,Cousin MA

doi

10.1016/j.jneumeth.2006.09.012

subject

Has Abstract

pub_date

2007-03-15 00:00:00

pages

197-205

issue

2

eissn

0165-0270

issn

1872-678X

pii

S0165-0270(06)00454-7

journal_volume

160

pub_type

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