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* These authors contributed equally
We describe here methods for inducing and analyzing olfactory experience-dependent remodeling of antennal lobe synaptic glomeruli in the Drosophila juvenile brain.
Early-life olfactory sensory experience induces dramatic synaptic glomeruli remodeling in the Drosophila juvenile brain, which is experientially dose-dependent, temporally restricted, and transiently reversible only in a short, well-defined critical period. The directionality of brain circuit synaptic connectivity remodeling is determined by the specific odorant acting on the respondent receptor class of olfactory sensory neurons. In general, each neuron class expresses only a single odorant receptor and innervates a single olfactory synaptic glomerulus. In the Drosophila genetic model, the full array of olfactory glomeruli has been precisely mapped by odorant responsiveness and behavioral output. Ethyl butyrate (EB) odorant activates Or42a receptor neurons innervating the VM7 glomerulus. During the early-life critical period, EB experience drives dose-dependent synapse elimination in the Or42a olfactory sensory neurons. Timed periods of dosed EB odorant exposure allow investigation of experience-dependent circuit connectivity pruning in juvenile brain. Confocal microscopy imaging of antennal lobe synaptic glomeruli is done with Or42a receptor-driven transgenic markers that provide quantification of synapse number and innervation volume. The sophisticated Drosophila genetic toolkit enables the systematic dissection of the cellular and molecular mechanisms mediating brain circuit remodeling.
The remodeling of juvenile brain circuits during early life represents the last chance for large-scale synaptic connectivity changes to match the highly variable, unpredictable environment into which an animal is born. As the most abundant group of animals, insects share this evolutionarily conserved, foundational critical period remodeling mechanism1. Critical periods open with the onset of sensory input, exhibit reversible circuit changes to optimize connectivity, and then close when stabilization forces resist further remodeling2. Insects are particularly reliant on olfactory sensory information and show a well-define....
1. Odorant exposure
Figure 1 shows the workflow for the olfactory experience-dependent critical period odorant exposure and brain imaging methods. The protocol starts with the age-matching of pharate dark pupae immediately prior to eclosion (Figure 1A). The pupae are placed into odorant chambers for 4 h, and then newly-eclosed adults are flipped into fresh vials in either the vehicle control or dosed EB odorant chambers (Figure 1B). We typically expose.......
The odorant exposure and brain imaging protocol presented here can be used to reliably induce and quantify experience-dependent olfactory sensory neuron synaptic glomeruli pruning during an early-life critical period. Earlier studies utilizing this treatment paradigm to explore olfactory circuit remodeling began odorant exposure on the 2nd day after eclosion3,4,5. In contrast, we begin odorant exposure in pharate pupa.......
We thank the other Broadie Lab members for their valuable input. Figures were created using BioRender.com. This work was supported by National Institute of Health grants MH084989 and NS131557 to K.B.
....Name | Company | Catalog Number | Comments |
For Odor Exposure | |||
Drosophila vials | Genesee Scientific | 32-110 | |
Ethyl butyrate | Sigma Aldrich | E15701 | |
Microcentrifuge tubes | Fisher Scientific | 05-408-129 | |
Mineral oil | Sigma Aldrich | M3516 | |
Odor chambers | Glasslock | ||
Paint brushes | Winsor & Newton | Series 233 | |
Parafilm | Thermofisher | S37440 | |
Wire mesh | Scienceware | 378460000 | |
Brain Dissection | |||
Ethanol, 190 proof | Decon Labs | 2801 | Diluted to 70% |
Forceps | Fine Science Tools | 11251-30 | Dumont #5 |
Paraformaldehyde | Electron Microscope Sciences | 157-8 | Diluted to 4% |
Petri dishes | Fisher Scientific | 08-757-100B | |
Phosphate-buffered saline | Thermo Fisher Scientific | 70011-044 | Diluted to 1x |
Sucrose | Fisher Scientific | BP220-1 | |
Sylgard | Electron Microscope Sciences | 24236-10 | |
Triton-X 100 | Fisher Scientific | BP151-100 | |
Brain Immunocytochemistry | |||
488 goat anti-chicken | Invitrogen | A11039 | |
546 goat anti-rat | Invitrogen | A11081 | |
Bovine serum albumin | Sigma Aldrich | A9647 | |
Chicken anti-GFP | Abcam | 13970 | |
Coverslips | Avantor | 48366-067 | 25 x 25 mm |
Double-sided tape | Scotch | 34-8724-5228-8 | |
Fluoromount-G | Electron Microscope Sciences | 17984-25 | |
Microscope slides | Fisher Scientific | 12-544-2 | 75 x 25 mm |
Nail polish | Sally Hansen | 109 | Xtreme Wear, Invisible |
Normal goat serum | Sigma Aldrich | G9023 | |
Rat anti-CadN | Developmental Studies Hybridoma Bank | AB_528121 | |
Confocal/Analysis | |||
Any computer/laptop | |||
Confocal microscope | Carl Zeiss | Zeiss 510 META | |
Fiji software | Fiji | Version 2.14.0/1.54f |
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