Paradoxical roles for programmed cell death signaling during viral infection of the central nervous system

被引:5
作者
Angel, Juan P. [1 ]
Daniels, Brian P. [1 ]
机构
[1] Rutgers State Univ, Dept Cell Biol & Neurosci, Piscataway, NJ 08854 USA
基金
美国国家卫生研究院;
关键词
PATHOGENESIS; APOPTOSIS; RIPK3; IL-1R1;
D O I
10.1016/j.conb.2022.102629
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Programmed cell death (PCD) is an essential mechanism of antimicrobial defense. Recent work has revealed an unexpected diversity in the types of PCD elicited during infection, as well as defined unique roles for different PCD modalities in shaping the immune response. Here, we review recent work describing unique ways in which PCD signaling operates within the infected central nervous system (CNS). These studies reveal striking complexity in the regulation of PCD signaling by CNS cells, including both protective and pathological outcomes in the control of infection. Studies defining the specialized molecular mechanisms shaping PCD responses in the CNS promise to yield much needed new insights into the pathogenesis of neuroinvasive viral infection, informing future therapeutic development.
引用
收藏
页数:7
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