2013
DOI: 10.1016/j.bbagen.2012.11.003
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Optical control of calcium-regulated exocytosis

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Cited by 15 publications
(19 citation statements)
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“…However, the large, step-function photocurrents provided by MAG and the calcium permeability of GluK2 40 make LiGluR-MAG more attractive to trigger calcium-regulated processes 39,41 including astrocyte activation 38 (see also Figure S7 in the Supporting Information). In cultured astrocytes expressing LiGluR-MAG (Figures 8), two-photon excitation at 820 nm triggered bistable currents (Figure 8c).…”
Section: Resultsmentioning
confidence: 99%
“…However, the large, step-function photocurrents provided by MAG and the calcium permeability of GluK2 40 make LiGluR-MAG more attractive to trigger calcium-regulated processes 39,41 including astrocyte activation 38 (see also Figure S7 in the Supporting Information). In cultured astrocytes expressing LiGluR-MAG (Figures 8), two-photon excitation at 820 nm triggered bistable currents (Figure 8c).…”
Section: Resultsmentioning
confidence: 99%
“…11 Even in cases where labeling, photoswitching, or the ligand efficacy remain submaximal, LiGluR constitutes a powerful tool for in vivo studies, as low-affinity kainate receptors like GluK2 are not fully activated in many physiological conditions either (see SI). LiGluR has been used to evoke patterns of action potentials in neurons, 12 reproducibly inject calcium into glial cells and chromaffin cells to evoke transmitter release, 13,14 excite specific cells for neural circuit analysis in vivo , 15 and restore a retinal light response and visual behavior to mice blinded by photoreceptor cell degeneration. 16 …”
mentioning
confidence: 99%
“…Another example is the exclusive activation of postsynaptic receptors, which allowed Kauwe et al to discover a novel plasticity mechanism that is induced post-synaptically and expressed pre-synaptically via a retrograde signal at the fly neuromuscular junction (Figure 4d) [37]. LiGluR has also been used to control Ca 2+ -influx into astrocytes to trigger gliotransmission (Figure 4c) [38], or to trigger exocytosis from neuroendocrine cells [39]. In addition, spatially-targeted 2-photon uncaging of glutamate has been applied at synapses in vivo in mice demonstrating the applicability of chemical based approaches in the mammalian brain (Figure 4e) [7].…”
Section: Optical Control Of Glutamate Receptors With Temporal Resolutmentioning
confidence: 99%