Method Article

Dissection of the Eye-Brain Complex from Fly Pupae: A Method to Isolate Retinal Tissue

April 30th, 2023

In This Article

Abstract

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Source: DeAngelis, M. W., Johnson, R. I. Dissection of the Drosophila Pupal Retina for Immunohistochemistry, Western Analysis, and RNA Isolation. J. Vis. Exp. (2019).

This video describes how to dissect and isolate the eye-brain complex from Drosophila pupae. The featured protocol demonstrates the procedure yielding high-quality tissue, compatible with, for example, immunostaining, as well as, other gene expression experiments.

Protocol

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This protocol is an excerpt from DeAngelis and Johnson, Dissection of the Drosophila Pupal Retina for Immunohistochemistry, Western Analysis, and RNA Isolation, J. Vis. Exp. (2019).

1. Tissue Preparation

  1. Set up Drosophila crosses (as described previously in Greenspan, Cold Spring Harbor Laboratory Press, (2004)) or culture specific Drosophila strains to obtain pupae of the desired genotype. To ensure that a large number of pupae emerge coincidently, establish these fly cultures in duplicate on nutrient-rich food media or standard food media generously supplemented wit....

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Results

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Drosophila pupae collection setup, pre-pupae on stick, larvae in vials, microcentrifuge tubes labeled.
Figure 1: Selection and culture of pupae for dissection. (A) Wandering third larval instar (L3) larvae and pupae locate along the sides of healthy Drosophila cultures. (B) Pre-pupae can be identified by their translucent white co.......

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Bamboo splints, 6"Ted Pella Inc116
Black dissecting dishGlass petri dish filled to rim with SYLG170 or SYLG184 (colored black with finely ground charcoal powder). <br/>Leave at room temperature for 24-48 h to polymerize.
Blade holderFine Science Tools10053
Bovine serum albuminSigma-AldrichA7906
Double-sided tape3M665
Drosophila&amp; food media, nutrient-rich7.5% sucrose, 15% glucose, 2.5% agar, 20% brewers yeast, 5% peptone, 0.125% MgSO4.7H2O, 0.125% CaCl2.2H20
Drosophila&amp; food media, standardBloomington Drosophila Stock center cornmeal recipe.<br/> (<a href="https://bdsc.indiana.edu/information/recipes/bloomfood.html" target="_blank">https://bdsc.indiana.edu/information/recipes/bloomfood.html</a>)
Fixative solution4% formadehyde in PBS, pH 7.4.
ForcepsFine Science Tools91150-20Forceps should be sharpened frequently.
FormaldehydeThermo Scientific28908
Glass 9-well dishesCorning7220-85Also known as 9-well dishes
Glass coverslips (22 x 22 mm)Fisher Scientific12-542-B
Glass microscope slides (25 x 75 x 1 mm)Fisher Scientific12-550-413
Glass petri dishCorning3160-100BO
GlycerolSigma-AldrichG5516
Microcentrigure tubesAxygenMCT-175-C
Microdissection scissorsFine Science Tools15000-03
Microwell trays (72 x 10 &micro;L wells)Nunc438733
Mounting media0.5% N-propylgallate and 80% glycerol in PBS
N-propylgallateSigma-AldrichP3130
PBS (phosphate buffered saline pH 7.4)Sigma-AldrichP5368Prepare according to manufacturer's instructions
PBT0.15% TritonX and 0.5% bovine serum albumin in PBS, pH 7.4
Pin holderFine Science Tools26016-12
Primary antibody: goat anti-GAPDHImgenexIMG-3073For Western blotting. Used at 1:3000
Primary antibody: rabbit anti-cleaved Dcp-1Cell signaling9578SFor immunofluorescence. Used at 1:100
Primary antibody: rat anti-DEcadDevelopmental Studies Hybridoma BankDCAD2For immunofluorescence. Used at 1:20
Primary antibody: rat anti-DEcadDOI: 10.1006/dbio.1994.1287DCAD1Gift from Tadashi Uemura. Used at 1:100.
Scalpel bladesFine Science Tools10050Break off small piece of scapel blade and secure in blade holder.
Secondary antibody: 488-conjugated donkey anti-rat IgG (H+L)Jackson ImmunoResearch712-545-153For immunofluorescence. Used at 1:200
Secondary antibody: cy3-conjugated goat anti-rabbit IgG (H+L)Jackson ImmunoResearch111-165-144For immunofluorescence. Used at 1:100
Secondary antibody: HRP-conjugated goat anti-rat IgG (H+L)Cell Signaling Technology7077For Western blotting. Used at 1:3000
Secondary antibody: HRP-conjugated rabbit anti-goat IgG (H+L)Jackson ImmunoResearch305-035-003For Western blotting. Used at 1:3000
Stereo dissecting microscope (M60 or M80)Leica Microsystemsor similar microscope
Sylgard (black)Dow CorningSYLG170
Sylgard (transparent)Dow CorningSYLG184Color black with finely ground charcol powder
Tissue: KimwipesKIMTECH34120
TritonXSigma-AldrichT8787
Tungsten needle, fineFine Science Tools10130-10Insert into pin holder
Tungsten needle, sturdyFine Science Tools10130-20Insert into pin holder
Yeast paste(local supermarket)Approximately 2 tablespoons Fleischmann's ActiveDry Yeast (or similar) dissolved in ~20 mL distilled H2O

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Tags

Drosophila Pupae DissectionEye Brain Complex IsolationRetinal Tissue ExtractionPupal Retina DissectionMicrodissection ScissorsStereo MicroscopeForceps TechniquePBS BufferThorax IncisionHead Capsule Removal

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