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Method Article

TACI: An ImageJ Plugin for 3D Calcium Imaging Analysis

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DOI:

10.3791/64953

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December 16th, 2022

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In This Article

Summary

TrackMate Analysis of Calcium Imaging (TACI) is an open-source ImageJ plugin for 3D calcium imaging analysis that examines motion on the z-axis and identifies the maximum value of each z-stack to represent a cell's intensity at the corresponding time point. It can separate neurons overlapping in the lateral (x/y) direction but on different z-planes.

Abstract

Research in neuroscience has evolved to use complex imaging and computational tools to extract comprehensive information from data sets. Calcium imaging is a widely used technique that requires sophisticated software to obtain reliable results, but many laboratories struggle to adopt computational methods when updating protocols to meet modern standards. Difficulties arise due to a lack of programming knowledge and paywalls for software. In addition, cells of interest display movements in all directions during calcium imaging. Many approaches have been developed to correct the motion in the lateral (x/y) direction.

This paper describes a workflow using a new ImageJ plugin, TrackMate Analysis of Calcium Imaging (TACI), to examine motion on the z-axis in 3D calcium imaging. This software identifies the maximum fluorescence value from all the z-positions a neuron appears in and uses it to represent the neuron's intensity at the corresponding t-position. Therefore, this tool can separate neurons overlapping in the lateral (x/y) direction but appearing on distinct z-planes. As an ImageJ plugin, TACI is a user-friendly, open-source computational tool for 3D calcium imaging analysis. We validated this workflow using fly larval thermosensitive neurons that displayed movements in all directions during temperature fluctuation and a 3D calcium imaging dataset acquired from the fly brain.

Introduction

The level of intracellular calcium is a precise marker of neuronal excitability. Calcium imaging measures the changes in intracellular calcium to understand neuronal activity1. Studies in neuroscience have increasingly used this method due to the development of techniques for measuring intracellular calcium concentration, including genetically encoded calcium indicators (GECIs), such as GCaMP2,3, which can be noninvasively expressed in specific sets of neurons through genetic approaches. The lower costs of lasers and microscope components have also increased the use of calcium imaging

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Protocol

1. Calcium imaging

  1. Fly larvae preparation
    NOTE: Flies and larvae are maintained at 25 °C under a 12 h:12 h light:dark cycle.
    1. Anesthetize the flies with CO2. Sort 20-45 males and 20-45 females into each fly vial, and give them at least 24 h to 48 h to recover from the CO2 exposure.
      NOTE: Fly exposure to CO2 should last for the shortest amount of time possible.
    2. To synchronize the larvae age, tap over the flies into new vials containing yeast granules, and allow them 4-8 h to lay eggs. Remove the flies by flipping them into new vials.
    3. Collect the larvae at 72 h usin....

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Results

Workflow of 3D calcium imaging analysis
In this study, we developed a new ImageJ plugin, TACI, and described a workflow to track z-drift and analyze 3D calcium imaging that pinpoints the responses of individual cells appearing in multiple z-positions (Figure 1). This tool has four functions: RENAME, ORGANIZE, EXTRACT, and MERGE. First, if the image names are not compatible with the ORGANIZE

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Discussion

This study developed a new ImageJ plugin, TACI, and described a workflow analyzing 3D calcium imaging. Many currently available tools focus on correcting the x/y motion, although motion on the z-axis also needs to be explicitly diagnosed or corrected6. During image acquisition in a live organism, movement on the z-axis is unavoidable even when the organism is immobilized, and some stimuli, such as temperature change, often cause significant z-drift. Increasing the height of the z-stacks will allow.......

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Disclosures

The authors have no conflicts of interest to disclose.

Acknowledgements

A Zeiss LSM 880 in the Fralin Imaging Center was used to collect the calcium imaging data. We acknowledge Dr. Michelle L Olsen and Yuhang Pan for their assistance with the IMARIS software. We acknowledge Dr. Lenwood S. Heath for constructive comments on the manuscript and Steven Giavasis for comments on the GitHub README file. This work was supported by NIH R21MH122987 (https://www.nimh.nih.gov/index.shtml) and NIH R01GM140130 (https://www.nigms.nih.gov/) to L.N. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Blunt Fill NeedelBD303129
Calcium chloride dihydrateFisher Scientific 10035-04-8Fly food ingredient
Carbon dioxideAirgasUN1013Size 200 High Pressure Steel Cylinder
CO2 bubbler kitGenesee59-180
Confocal microscope LSM880Zeiss4109002107876000An inverted Axio Observer Z1, equipped with 5 lasers, 2 standard PMT detectors, 32-channel GaAsP dectectors, an Airyscan detector, and Definite Focus.2.
DAQami softwareMeasurement Computing
DextroseGenesee62-113Fly food ingredient
Drosophila AgarGenesee66-111Fly food ingredient
EthanolDecon Labs, Inc.64-17-5Fly food ingredient
Fly line: Ir21a-Gal4Dr. Paul Garrity labA kind gift
Fly line: Ir21a-Gal80Dr. Lina Ni lab
Fly line: Ir68a-Gal4Dr. Aravinthan DT Samuel labA kind gift
Fly line: Ir93a-Gal4Dr. Paul Garrity labA kind gift
Fly line: UAS-GCaMP6Bloomington Drosophila Stock Center42750
FlypadGenesee59-114
General purpose forged brass regulatorGentecG152
Gibco PBS pH 7.4 (1x)Thermo Fisher Scientific10010-031
Green Drosophila tubingGenesee59-124
Heat transfer compoundMG Chemicals860-60G
HeatsinkDigi-Key ElectronicsATS2193-NDResize to 12.9 x 5.5 cm
IlluminatorAmScopeLED-6W
Inactive Dry YeastGenesee62-108Fly food ingredient
IncubatorPervicalDR-41VLLight: dark cycle: 12h:12h; temperature: 25 °C; humidity: 40-50% RH.
Methyl-4-hydroxybenzoateThermo Scientific126965000Fly food ingrediete
Micro cover glassVWR 48382-12622 x 40 mm
Microscope slidesFisher Scientific 12-544-225 x 75 x 1.0 mm
Nail polishKleancolor
Narrow Drosophila vialsGenesee32-113RL
Objective Zeiss420852-9871-000LD LCI Plan-Apochromat 25x/0.8 Imm Corr DIC M27
Peltier cooling moduleTE TechnologyTE-127-1.0-0.830 x 30 mm
PlugsGenesee49-102
Power SupplyCircuit SpecialistsCSI1802X10 volt DC 2.0 amp linear bench power supply
Princeton Artist Brush NepturePrinceton Artist Brush Co.Series 4750, size 2
Sodium potassium L-tartrate tetrahydrateThermo Scientific033241-36Fly food ingredient
Stage insert Wienecke and Sinske432339-9030-000
Stereo MicroscopeOlympusSZ61Any stereo microscope works
T-FittingGenesee59-123
Thermocouple data acquisition deviceMeasurement ComputingUSB-2001-TCSingle channel
Thermocouple microprobePhysitempIT-24P 
Yellow CornmealGenesee62-101Fly food ingredient
Z-axis piezo stageWienecke and Sinske432339-9000-000

References

  1. Grienberger, C., Konnerth, A. Imaging calcium in neurons. Neuron. 73 (5), 862-885 (2012).
  2. Nakai, J., Ohkura, M., Imoto, K. A high signal-to-noise Ca(2+) probe composed of a single green fluorescent protein. Nature Biotechnology. 19 (2), 137-141 (2001).
  3. Zhang, Y.....

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