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Method Article

Calcium Imaging in Individual Neurons Regulating Egg-Laying Behavior in Caenorhabditis elegans

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July 8th, 2025

In This Article

Abstract

Source: Ravi, B. et al., Ratiometric Calcium Imaging of Individual Neurons in Behaving Caenorhabditis Elegans. J. Vis. Exp. (2018).

This video demonstrates a technique for calcium imaging in individual neurons of behaving Caenorhabditis elegans using genetically encoded fluorescent reporter proteins. It outlines the steps involved in imaging worm movement and measuring reporter fluorescence ratios from neurons to correlate intracellular calcium levels with neuronal activity and behavioral changes during egg-laying.

Protocol

1. Strains, Culture Media, and Mounting of Animals

  1. Grow C. elegans worms at 20 °C on standard 60-mm Nematode Growth Medium (NGM) agar plates seeded with OP50 E. coli bacterial food.
  2. Prepare two plasmids for each cell-specific promoter of interest: one, driving expression of GCaMP5 to record intracellular Ca2+, and the second, driving expression of mCherry to allow for ratiometric quantitation of GCaMP5 fluorescence changes and simplify object finding and measurement.
    NOTE: GCaMP5:mCherry ratiometric imaging corrects for fluctuations in GCaMP5 fluorescence that result from ....

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Results

C. elegans behavior assay setup diagram with OP50, plate, worms, and eggs for experimental study.
Figure 1. C. elegans mounting technique for high-resolution imaging of egg-laying circuit activity and behavior. Top, the final mount from the side. Bottom, the final mount as viewed through the bottom of the large coverslip. Arro.......

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Disclosures

No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
C. elegans growth, cultivation, and mounting
Escherichia coli bacterial strain, OP50Caenorhabditis Genetic CenterOP50Food for C. elegans. Uracil auxotroph. E. coli B. Biosafety Level 1
HSN GCaMP5+mCherry worm strainCaenorhabditis Genetic CenterLX2004Integrated transgene using nlp-3 promoter to drive GCaMP5 and mCherry expression in HSN. Full genotype:
vsIs183 [nlp-3p::GCaMP5::nlp-3 3'UTR + nlp-3p::mCherry::nlp-3 3'UTR + lin-15(+)], lite-1(ce314), lin-15(n765ts) X
lite-1(ce314), lin-15(n765ts) mutant strain for transgene preparationauthorLX1832Strain for recovery of high-copy transgenes after microinjection with pL15EK lin-15(n765ts) rescue plasmid. Also bears the linked lite-1(ce314) mutation which reduces blue-light sensitivity. Available from author by request
pL15EK lin-15a/b genomic rescue plasmidauthorpL15EKRescue plasmid for recovery of transgenic animals after injection into LX1832
lite-1(ce314), lin-15(n765ts) X strain. Available from author by request
pKMC299 plasmidauthorpKMC299Plasmid for expression of mCherry in the HSNs from the nlp-3 promoter. Has nlp-3 3' untranslated region
pKMC300 plasmidauthorpKMC300Plasmid for expression of GCaMP5 in the HSNs from the nlp-3 promoter. Has nlp-3 3' untranslated region
Potassium Phosphate MonobasicSigmaP8281For preparation of NGM plates
Potassium Phosphate DibasicSigmaP5655For preparation of NGM plates
Magnesium Sulfate HeptahydrateAmresco662For preparation of NGM plates
Calcium Chloride DihydrateAlfa Aesar12312For preparation of NGM plates
PeptoneBecton Dickinson211820For preparation of NGM plates
Sodium ChlorideAmresco241For preparation of NGM plates
CholesterolAlfa AesarA11470For preparation of NGM plates
Agar, Bacteriological Type A, UltrapureAffymetrix10906For preparation of NGM plates
60 mm Petri dishesVWR25384-164 For preparation of NGM plates
24 x 60 mm micro cover glasses, #1.5VWR48393-251Cover glass through which worms are imaged
22 x 22 mm micro cover glasses, #1VWR48366-067Cover glass that covers the top of the agar chunk
Stereomicroscope with transmitted light baseLeicaM50Dissecting microscope for worm strain maintenance, staging, and mounting
Platinum iridium wire, (80:20), 0.2mmALFA AESARAA39526-BWFor worm transfer
Calcium imaging microscope
Anti-vibration air tableTMC63-544Micro-g' Lab Table 30" x 48" anti-vibration table with 4" CleanTop M6 on 25mm top
Inverted compound microscopeZeiss431007-9902-000Axio Observer.Z1 inverted microscope
Sideport L80/R100 (3 position)Zeiss425165-0000-000To divert 20% of output to brightfield (CMOS) camera, 80% to fluorescence (sCMOS) camera
Tilt Back Illumination CarrierZeiss423920-0000-000For infrared/behavior imaging
Lamphousing 12V/100W w/ CollectorZeiss423000-9901-000For infrared/behavior imaging
Halogen lamp 12V/100WZeiss380059-1660-000For infrared/behavior imaging. White-light LEDs do not emit significant infrared light, so they will not allow brightfield imaging after the infrared bandpass filter
32 mm Infrared bandpass filter (750-790 nm) for Halogen lampZeiss447958-9000-000BP 750-790; DMR 32mm, for infrared illumination for brightfield and behavior
6-filter Condenser Turret (LD 0.55 H/DIC/Ph), MotorizedZeiss424244-0000-000For infrared/behavior imaging
Condenser & ShutterZeiss423921-0000-000For infrared/behavior imaging
Binocular eyepiece with phototube for infrared CMOS cameraZeiss425536-0000-000For infrared/behavior imaging
Eyepiece 10x, 23mmZeiss444036-9000-000For worm localization on the agar chunk
C-Mount Adapter 2/3" 0.63x demagnifierZeiss426113-0000-000Mount for infrared CMOS camera
CMOS camera for infrared brightfield and behavior (1" sensor)FLIR (formerly Point Grey Research)GS3-U3-41C6NIR-CCamera for brightfield imaging
USB 3.0 Host Controller CardFLIR (formerly Point Grey Research)ACC-01-1202Fresco FL1100, 4 Ports
8 pins, 1m GPIO Cable, Hirose HR25 Circular Connector FLIR (formerly Point Grey Research)ACC-01-3000Cable for TTL triggering. The green wire connects to GPIO3 / Pin 4 and the brown wire connects to Ground / Pin 5
Plan-Apochromat 20x/0.8 WD=0.55 M27Zeiss420650-9901-000Best combination of magnification, numerical aperture, and working distance
6-cube Reflector Turret, MotorizedZeiss424947-0000-000For fluorescence imaging
Fluorescence Light Train, MotorizedZeiss423607-0000-000For fluorescence imaging
Fluorescence ShutterZeiss423625-0000-000For fluorescence imaging
GFP and mCherry dual excitation and emission filter cube (for microscope)Zeiss489062-9901-000FL Filter Set 62 HE BFP+GFP+HcRed for fluorescence imaging
LED illumination systemZeiss423052-9501-000Triggerable Colibri.2 LED system for fluorescent illumination
GFP LED module (470 nm)Zeiss423052-9052-000Colibri.2 LED for GFP fluorescence excitation
mCherry LED module (590 nm)Zeiss423052-9082-000Colibri.2 LED for mCherry fluorescence excitation
Iris stop slider for incident-light equipmentZeiss000000-1062-360Field aperture iris to limit LED illumination to the camera field of view
C-Mount Adapter 1" 1.0xZeiss426114-0000-000Adapter for image-splitter and sCMOS fluorescence camera
Image splitterHamamatsuA12801-01Gemini W-View, other image splitters may be used, but they may not be optimized for the large sensor size of the sCMOS cameras
GFP / mCherry dichroic mirror (image splitter)SemrockDi02-R594-25x36Splitting GCaMP5 from mCherry and infrared signals
GFP emission filter (image splitter)SemrockFF01-525/30-25Capturing GCaMP5 fluorescence
mCherry/ emission filter (image splitter)SemrockFF01-647/57-25This filter is necessary to exclude the infrared light used for brightfield imaging
sCMOS camera for fluorescence (1" sensor)HamamatsuA12802-01 / C11440-22CUOrca FLASH 4.0 V2. Newer models allow for separate image acquisition settings on separate halves of the sensor, allowing acquisition of two-channel images in combination with an image splitter
Motorized XY StageMärzhäuserSCAN IM 130 x 100Stage movement; the XY resolution of this stage is 0.2µm per step
XY Stage controller with joystickLUDLMAC6000, XY joystickManual tracking of worms. MAC6000 controller should be connected to the PC through the serial (RS-232) port configured to 115200 baud
Digital Acquisition board (DAQ)ArduinoUnoReceiving TTL triggers from sCMOS camera. The Uno should be loaded with the standard Firmata package, and the computer USB port configured to 57600 baud
BNC Male to BNC Male Cable - 6 ftHosa TechnologyHOBB6BNC connectors for TTL triggering
Gold-Plated BNC Male to SMA male coaxial cable (8.8")uxcell6.08642E+11To connect the fluorescence camera trigger outputs
BNC turn head adapterHantekRRBNCTH21BNC to Banana Plug Adapter (4mm)
BNC female to female connectorDiageng20130530009Female to female BNC adapter to connect the BNC output from the camera to the Banana Plug
Solderless flexible breadboard jumper wiresZ&TGK1212827To connect the BNC trigger outputs to the Arduiono DAQ. Male to male.
High performace workstationHPZ820Windows 7, 64GB RAM, Dual Xeon processor, solid state C: drive, serial (RS-232) port, multiple PCIe3 slots for ethernet connectivity, USB 3.0 cards, and additional solid state drives
M.2 Solid state driveSamsungMZ-V5P512BWHigh-speed streaming and analysis of image data
M.2 Solid state drive adapter for workstationsLycomDT-120M.2 to PCIe 3.0 4-lane adapter
Network attached storageSynologyDS-2415+Imaging data storage and analysis
Hard disk drivesWestern DigitalWD80EFZXRED 8 TB, 5400 RPM Class SATA 6 Gb/s 128MB Cache 3.5 Inch. Storage of imaging data (10 drives + 2 drive redundancy)
Software
Fluorescence AcquisitionHamamatsuHCImage DIARecording of two channel (GCaMP5 and mCherry) fluorescence image sequences at 20 fps
Brightfield AcquisitionFLIR (formerly Point Grey Research)FlycaptureRecording of brightfield JPEG image sequences
Stage Serial Port ReaderBonsaihttps://bitbucket.org/horizongir/bonsaiFacilitates tracking of worms during behavior
LED controller softwareZeissMicro Toolbox Test 2011To set up the intensity and trigger inputs for the different LEDs in the Colibri.2 unit
ImageJ NIHhttps://imagej.net/Fiji/DownloadsSimple review of image sequences and formatting changes for import into Ratiometric Quantitation software
ExcelMicrosoft 2002984-001-000001For generating subsets of comma-separated value data from Volocity for MATLAB analysis
Peak FindingMATLABR2017aScript used for Ratio peak feature calculations
Ratiometric QuantitationPerkin ElmerVolocity 6.3Facilitates calculation of ratiometric image channels, image segmentation for object finding, and ratio measurement of found objects
Scripts
AnalyzeGCaMP_2017.mMATLABMean Ratio and XY centroid scriptAnalyzes a ratiometric output in .csv format, consolidating objects and centroid positions, calculating ratio changes (ΔR/R), identifying peaks and peak features, and writing plots (with and without annotated peaks) in postscript format. For matrix file import, the script will output data into three folders: analyzed, peaks, and traces. 'Analyzed' output is a matrix file of the consolidated objects with six columns (units): time (s), area (square microns), ratio, X centroid (microns), Y centroid (microns), and ΔR/R. 'Peaks' output is a matrix file of the timepoints of found peaks, the amplitude (in ΔR/R), the peak width (s), and the prominance of the peak. 'Traces' output are postscript files of calcium traces.
XY-stage-final.bonsaiBonsaiTTL-triggered DAQ and stage position serial port readerRecords X and Y stage position (in microns) when the attached Arduino receives a positive TTL signal from sCMOS camera during frame exposure. Script writes a .csv file with four columns: frame number, X position (microns), Y position (microns), and the time elapsed between frames (typically ~50 msec when recording at 20 fps). X and Y stage position from this output (columns 2 and 3, respectively) are added to the X and Y centroid positions from the AnalyzeGCaM

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