Drosophila innate immune response pathways moonlight in neurodegeneration

被引:12
|
作者
Petersen, Andrew J. [1 ,2 ]
Wassarman, David A. [1 ,2 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Mol & Cellular Pharmacol Program, Madison, WI 53706 USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Dept Cell & Regenerat Biol, Madison, WI USA
关键词
antimicrobial peptide; ATM; glial cell; Imd; neuron; NF kappa B; Toll; BRAIN DEGENERATION; MELANOGASTER; PATHOGENESIS; EXPRESSION; RHODOPSIN; TOXICITY; ARRESTIN; MUTANTS; GENES; ATM;
D O I
10.4161/fly.20999
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this Extra View, we highlight recent Drosophila research that has uncovered a new role for the innate immune response. The research indicates that, in addition to combating infection, the innate immune response promotes neurodegeneration. Our publication (Petersen et al., 2012) reveals a correlative relationship between the innate immune response and neurodegeneration in a model of the human disease Ataxia-telangiectasia (A-T). We also found that glial cells are responsible for the innate immune response in the A-T model, and work by others implicates glial cells in neurodegeneration. Additionally, publications by Chinchore et al. (2012) and Tan et al. (2008) reveal a causative role for the innate immune response in models of human retinal degenerative disorders and Alzheimer disease, respectively. Collectively, these findings suggest that activation of the innate immune response is a shared cause of neurodegeneration in different human diseases.
引用
收藏
页码:169 / 172
页数:4
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