The choroid plexus and the paradox of interferons in the aging brain

被引:3
作者
Dhib-Jalbut, Suhayl [1 ]
机构
[1] RUTGERS Robert Wood Johnson Med Sch, Dept Neurol, New Brunswick, NJ 08901 USA
关键词
Interferon; Choroid plexus; Aging; Neurogenesis; Neuroinflammation; MULTIPLE-SCLEROSIS;
D O I
10.1016/j.cyto.2014.11.021
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
The choroid plexus (CP) function is largely viewed as the source of cerebrospinal fluid (CSF) and as a barrier between the blood and the CSF. Other functions of the CP are becoming increasingly recognized as in the recent publication by Baruch et. al. who demonstrate increased expression of interferon type I mRNA signature (irf7, ifnss and ifit1) in CP of aged brains compared to younger brains, whereas interferon type II dependent genes (icam1, cxcl10, and ccl17) are reduced in the aging CP. The authors speculate an IFN-dependent mechanism that plays a role in the aging process and cognitive decline. This short communication summarizes the findings by the authors and highlights the seemingly paradoxical roles of IFN type I and type II in neuroinflammation. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:413 / 414
页数:2
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