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- W2005037250 abstract "As one of the most important second messengers, calcium in nerve cells plays a critical role in neuronal processes,including excitability, neurotransmitter release, synaptic plasticity. Modulation of the calcium concentration is animportant means of regulating diverse neuronal functions. To evaluate the role of calcium, quantitative measurement ofcytosolic free calcium concentrations is necessary. There are several optical techniques that are available formeasurement of calcium in live cells. Laser scanning confocal microscopy and two-photon microscopy are two prevalenttechniques for their advantage in spatial resolution. In this paper, calcium in dorsal root ganglion neurons was imaged bylaser scanning confocal microscopy and two-photon microscopy with Fluo-3, a calcium specific fluorescence probe.Both of spatial resolution and photobleaching, two common limitations of optical image modality, were comparedbetween laser scanning confocal microscopy and two-photon microscopy, respectively. Three dimension images showedthat laser scanning confocal microscopy and two-photon microscopy had not only similar lateral resolution but alsoparallel vertical resolution. However, Laser scanning confocal microscopy had an advantage over the two-photonmicrocopy in photobleaching. These results indicated that laser scanning confocal microscopy was more suitable thantwo-photon microscopy to be applied in imaging calcium in dorsal root ganglion neurons with Fluo-3." @default.
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- W2005037250 date "2012-02-09" @default.
- W2005037250 modified "2023-09-22" @default.
- W2005037250 title "Comparison of calcium imaging in dorsal root ganglion neurons by using laser scanning confocal and two-photon microscopy" @default.
- W2005037250 doi "https://doi.org/10.1117/12.908220" @default.
- W2005037250 hasPublicationYear "2012" @default.
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