Assessment of autophagic flux assay in the adult Drosophila brain

Mel Feany

Published: 2024-01-30 DOI: 10.17504/protocols.io.bp2l6x661lqe/v1

Abstract

Transgenic flies expressing GFP-mCherry-Atg8a (obtained from the Bloomington  Drosophila  Stock Center)  

under the control of the  neuronal nSyb-GAL4 driver are used for assaying autophagic flux.

Steps

1.

Transgenic flies expressing GFP-mCherry-Atg8a (obtained from the Bloomington  Drosophila  Stock Center)  under the control of the  neuronal nSyb-GAL4 driver are used for assaying autophagic flux

2.

Brains from 10-day-old animals are dissected in ice-cold 1X PBS

3.

The dissected brain are transferred to a glass slide

4.

The remaining 1X PBS is removed from the slide

5.

A drop of DAPI Fluoromount is added and the brain mounted with a coverslip

6.

The dissected brain is imaged immediately within 5 minutes using a Zeiss confocal microscope under a 63X objective lens, and a line scan performed

7.

For quantification, the intensity of GFP and mCherry is measured per puncta using ImageJ, and the ratio between GFP and mCherry calculated

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