Calcium imaging was performed as described elsewhere [37 (link),41 (link)]. Briefly, a single adult animal that expressed genetically encoded calcium indicator GCaMP3 [59 (link)] and/or XCaMP-R [60 (link)] was placed on a 10% agar pad on a cover slip with 0.1 μm polystyrene beads (Polysciences, Warrington, PA, USA) and covered by another cover slip for immobilization [92 (link)]. The immobilized animals were placed on a Peltier-based temperature controller (Tokai Hit, Fujinomiya, Japan) on a stage of BX61WI microscope (Olympus, Tokyo, Japan). The red and green fluorescence was separated by the Dual-View optics system (Molecular Devices, Sunnyvale, CA, USA), and the images were captured by an EM-CCD camera C9100-13 ImageEM (Hamamatsu Photonics, Japan) at 1 frame per second. Excitation pulses were generated by SPECTRA light engine (Lumencor, Beaverton, OR, USA). The fluorescence intensities were measured by the MetaMorph imaging system (Molecular Devices).
Imaging Expression and Calcium Dynamics
Calcium imaging was performed as described elsewhere [37 (link),41 (link)]. Briefly, a single adult animal that expressed genetically encoded calcium indicator GCaMP3 [59 (link)] and/or XCaMP-R [60 (link)] was placed on a 10% agar pad on a cover slip with 0.1 μm polystyrene beads (Polysciences, Warrington, PA, USA) and covered by another cover slip for immobilization [92 (link)]. The immobilized animals were placed on a Peltier-based temperature controller (Tokai Hit, Fujinomiya, Japan) on a stage of BX61WI microscope (Olympus, Tokyo, Japan). The red and green fluorescence was separated by the Dual-View optics system (Molecular Devices, Sunnyvale, CA, USA), and the images were captured by an EM-CCD camera C9100-13 ImageEM (Hamamatsu Photonics, Japan) at 1 frame per second. Excitation pulses were generated by SPECTRA light engine (Lumencor, Beaverton, OR, USA). The fluorescence intensities were measured by the MetaMorph imaging system (Molecular Devices).
Corresponding Organization : Institut d'Investigació Biomédica de Bellvitge
Variable analysis
- Expression of OLA-1::GFP and ZYG-8::GFP in head region
- Expression of OLA-1::GFP in the whole body
- Temperature of the Peltier-based temperature controller
- Fluorescence intensities of OLA-1::GFP and ZYG-8::GFP
- Calcium dynamics (measured by GCaMP3 and/or XCaMP-R fluorescence)
- Microscopes used (BX53 upright microscope and LSM880 confocal microscope)
- Immobilization of the animals on a 10% agar pad with 0.1 μm polystyrene beads
- Excitation pulses generated by SPECTRA light engine
- Fluorescence intensity measurements using the MetaMorph imaging system
- Positive control: None explicitly mentioned
- Negative control: None explicitly mentioned
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