Neurodegenerative disorders and sterile inflammation: lessons from a Drosophila model

J Biochem. 2019 Sep 1;166(3):213-221. doi: 10.1093/jb/mvz053.

Abstract

Central nervous system (CNS)-related disorders, including neurodegenerative diseases, are common but difficult to treat. As effective medical interventions are limited, those diseases will likely continue adversely affecting people's health. There is evidence that the hyperactivation of innate immunity is a hallmark of most neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis and polyglutamine diseases. In mammalian and fly CNS, the presence of noninfectious ligands, including danger-associated molecular patterns, is recognized by (micro)glial cells, inducing the expression of proinflammatory cytokines. Such inflammation may contribute to the onset and progression of neurodegenerative states. Studies using fruit flies have shed light on the types of signals, receptors and cells responsible for inducing the inflammation that leads to neurodegeneration. Researchers are using fly models to assess the mechanisms of sterile inflammation in the brain and its link to progressive neurodegeneration. Given the similarity of its physiological system and biochemical function to those of mammals, especially in activating and regulating innate immune signalling, Drosophila can be a versatile model system for studying the mechanisms and biological significance of sterile inflammatory responses in the pathogenesis of neurodegenerative diseases. Such knowledge would greatly facilitate the quest for a novel effective treatment for neurodegenerative diseases.

Keywords: Drosophila; CNS; innate immunity; neurodegenerative diseases; sterile inflammation.

Publication types

  • Review

MeSH terms

  • Animals
  • Disease Models, Animal*
  • Drosophila* / immunology
  • Inflammation / drug therapy
  • Inflammation / immunology
  • Inflammation / metabolism*
  • Neurodegenerative Diseases / drug therapy
  • Neurodegenerative Diseases / immunology
  • Neurodegenerative Diseases / metabolism*