Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9409
Title: A Simple Immunofluorescence Method to Characterize Neurodegeneration and Tyrosine Hydroxylase Reduction in Whole Brain of a Drosophila Model of Parkinson’s Disease
Authors: Chaurasia, Rahul
Ayajuddin, Mohamad
RATNAPARKHI, GIRISH S.
Lingadahalli, Shashidhara S.
Yenisetti, Sarat C.
Dept. of Biology
Keywords: Drosophila
Dopaminergic neurodegeneration
Fluorescence intensity
Tyrosine hydroxylase
Tissue imaging
Fluorescence microscope
2024
Issue Date: Feb-2024
Publisher: Bio-protocol LLC
Citation: Bio-protocol, 14(04).
Abstract: Dopaminergic (DAergic) neurodegeneration in the substantia nigra pars compacta of the human brain is the pathological feature associated with Parkinson’s disease (PD). Drosophila also exhibits mobility defects and diminished levels of brain dopamine on exposure to neurotoxicants mimicking PD. Our laboratory demonstrated in a Drosophila model of sporadic PD that there is no decrease in DAergic neuronal number; instead, there is a significant reduction in tyrosine hydroxylase (TH) fluorescence intensity (FI). Here, we present a sensitive assay based on the quantification of FI of the secondary antibody (ab). As the FI is directly proportional to the amount of TH synthesis, its reduction under PD conditions denotes the decrease in the TH synthesis, suggesting DAergic neuronal dysfunction. Therefore, FI quantification is a refined and sensitive method to understand the early stages of DAergic neurodegeneration. FI quantification is performed using the ZEN 2012 SP2 single-user software; a license must be acquired to utilize the imaging system to interactively control image acquisition, image processing, and analysis. This method will be of good use to biologists, as it can also be used with little modification to characterize the extent of degeneration and changes in the level of degeneration in response to drugs in different cell types. Unlike the expensive and cumbersome confocal microscopy, the present method will be an affordable option for fund-constrained neurobiology laboratories.
URI: https://doi.org/10.21769/BioProtoc.4937
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9409
ISSN: 2331-8325
Appears in Collections:JOURNAL ARTICLES

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