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An interplay between immune response and neurodegenerative disease progression: An assessment using Drosophila as a model
- Source :
- Journal of neuroimmunology. 346
- Publication Year :
- 2020
-
Abstract
- Neurodegeneration, the slow and progressive loss of neurons in the central nervous system has become a major challenge to public health worldwide particularly with elderly people. Until recently, the brain and immune system were studied exclusively, independent of each other representing two distinct systems. Recent studies ensue crosstalk between these two systems to maintain homeostasis. Though the progressive loss of specific neuronal subsets is a hallmark of neurodegenerative disease, emerging evidences indicate that immune response also plays a critical role in disease progression. Due to conservation of mechanisms that govern neural development and innate immune activation in flies and humans, and availability of powerful genetic tools, the fruit fly Drosophila melanogaster is one of the best model organisms to investigate the immune response in neurodegenerative disease. Owing to significant homology between human and Drosophila immune system and recent reports on interplay between immune system and neurodegenerative disease progression, the main focus of the review is to develop a comprehensive understanding of how neuro-immune interactions contribute to neurodegeneration using Drosophila as a model system.
- Subjects :
- Innate immune system
biology
ved/biology
Immunology
Neurodegeneration
ved/biology.organism_classification_rank.species
Disease
biology.organism_classification
medicine.disease
03 medical and health sciences
0302 clinical medicine
Immune system
Neurology
medicine
Immunology and Allergy
Neurology (clinical)
Drosophila melanogaster
Model organism
Neural development
Neuroscience
030217 neurology & neurosurgery
Neuroinflammation
030215 immunology
Subjects
Details
- ISSN :
- 18728421
- Volume :
- 346
- Database :
- OpenAIRE
- Journal :
- Journal of neuroimmunology
- Accession number :
- edsair.doi.dedup.....4614c5e10c604804540ef884d7101cf5