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Connecting Malfunctioning Glial Cells and Brain Degenerative Disorders
Author(s) -
Natalie Kaminsky,
Ofer Bihari,
Sivan Kanner,
Ari Barzilai
Publication year - 2016
Publication title -
genomics proteomics and bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.114
H-Index - 49
eISSN - 2210-3244
pISSN - 1672-0229
DOI - 10.1016/j.gpb.2016.04.003
Subject(s) - neuroscience , biology , medicine
The DNA damage response (DDR) is a complex biological system activated by different types of DNA damage. Mutations in certain components of the DDR machinery can lead to genomic instability disorders that culminate in tissue degeneration, premature aging, and various types of cancers. Intriguingly, malfunctioning DDR plays a role in the etiology of late onset brain degenerative disorders such as Parkinson's, Alzheimer's, and Huntington's diseases. For many years, brain degenerative disorders were thought to result from aberrant neural death. Here we discuss the evidence that supports our novel hypothesis that brain degenerative diseases involve dysfunction of glial cells (astrocytes, microglia, and oligodendrocytes). Impairment in the functionality of glial cells results in pathological neuro-glial interactions that, in turn, generate a "hostile" environment that impairs the functionality of neuronal cells. These events can lead to systematic neural demise on a scale that appears to be proportional to the severity of the neurological deficit.

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