2016
DOI: 10.1038/srep20619
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Gold nanoparticle-assisted all optical localized stimulation and monitoring of Ca2+ signaling in neurons

Abstract: Light-assisted manipulation of cells to control membrane activity or intracellular signaling has become a major avenue in life sciences. However, the ability to perform subcellular light stimulation to investigate localized signaling has been limited. Here, we introduce an all optical method for the stimulation and the monitoring of localized Ca2+ signaling in neurons that takes advantage of plasmonic excitation of gold nanoparticles (AuNPs). We show with confocal microscopy that 800 nm laser pulse application… Show more

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Cited by 57 publications
(47 citation statements)
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“…This magnetothermal approach to temporally and spatially control release of compounds in the brain may perhaps be compatible with other neuromodulation techniques that rely upon light in the visible (optogenetics) or possibly near infrared (direct or with plasmonic nanostructures) spectral range. The option of using such a tool alongside other stimuli could ultimately enable neuroscientists to design experiments that probe functional connectivity between distinct brain structures.…”
Section: Resultsmentioning
confidence: 95%
“…This magnetothermal approach to temporally and spatially control release of compounds in the brain may perhaps be compatible with other neuromodulation techniques that rely upon light in the visible (optogenetics) or possibly near infrared (direct or with plasmonic nanostructures) spectral range. The option of using such a tool alongside other stimuli could ultimately enable neuroscientists to design experiments that probe functional connectivity between distinct brain structures.…”
Section: Resultsmentioning
confidence: 95%
“…Media was replaced 1:1 every three days and cells were used at 7 DIV unless stated otherwise. For live STED recordings, rat hippocampal neurons were prepared as described previously 33 .…”
Section: Primary Neuronal Culturesmentioning
confidence: 99%
“…Both spontaneous and stimulated spiking activities provide unique information on the interactions of ion channels and synapses from single neurons to complex networks 5,6 . For decades, a number of techniques have been developed to record action potentials, including patch-clamps 7,8 , optical-probes 3,9,10 , multi-electrode arrays 6,11,12 , and several types of optical imaging modalities 4,5,10,11 . In particular, single/two-photon fluorescence microscopy has become one of the most powerful and popular approaches to monitoring ion dynamics of neuronal activities in large networks.…”
Section: Introductionmentioning
confidence: 99%