| Literature DB >> 32939758 |
Falguni Baidya1, Mariya Bohra1, Aishika Datta1, Deepaneeta Sarmah1, Birva Shah1, Priya Jagtap1, Swapnil Raut1, Ankan Sarkar1, Upasna Singh1, Kiran Kalia1, Anupom Borah2, Xin Wang3, Kunjan R Dave4, Dileep R Yavagal5, Pallab Bhattacharya1.
Abstract
Neurodegeneration is characterized by gradual onset and limited availability of specific biomarkers. Apart from various aetiologies such as infection, trauma, genetic mutation, the interaction between the immune system and CNS is widely associated with neuronal damage in neurodegenerative diseases. The immune system plays a distinct role in disease progression and cellular homeostasis. It induces cellular and humoral responses, and enables tissue repair, cellular healing and clearance of cellular detritus. Aberrant and chronic activation of the immune system can damage healthy neurons. The pro-inflammatory mediators secreted by chief innate immune components, the complement system, microglia and inflammasome can augment cytotoxicity. Furthermore, these inflammatory mediators accelerate microglial activation resulting in progressive neuronal loss. Various animal studies have been carried out to unravel the complex pathology and ascertain biomarkers for these harmful diseases, but have had limited success. The present review will provide a thorough understanding of microglial activation, complement system and inflammasome generation, which lead the healthy brain towards neurodegeneration. In addition to this, possible targets of immune components to confer a strategic treatment regime for the alleviation of neuronal damage are also summarized.Entities:
Keywords: complement system; immune system; inflammasome; microglia; neurodegenerative disease
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Year: 2020 PMID: 32939758 PMCID: PMC7808166 DOI: 10.1111/imm.13264
Source DB: PubMed Journal: Immunology ISSN: 0019-2805 Impact factor: 7.397