14-3-3 protein in CSF: An early predictor of SIVCNS disease

被引:16
作者
Helke, KL
Queen, SE
Tarwater, PM
Turchan-Cholewo, J
Nath, A
Zink, MC
Irani, DN
Mankowski, JL
机构
[1] Johns Hopkins Univ, Sch Med, Dept Comparat Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[3] Univ Texas, Hlth Sci Ctr, Sch Publ Hlth, Houston, TX USA
[4] Johns Hopkins Univ, Dept Neurol, Baltimore, MD 21218 USA
关键词
14-3-3; protein; CSF; HIV; marker; neurodegeneration; SIV;
D O I
10.1093/jnen/64.3.202
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
in neurons, 14-3-3 proteins regulate diverse processes, including signal transduction, neurotransmitter production, and apoptosis by binding to target proteins, but the role 14-3-3 proteins play in the pathogenesis of central nervous system (CNS) disease remains unclear. To examine the relationship between presence of 14-3-3 protein in cerebrospinal fluid (CSF) and encephalitis in the SIV/macaque model of HIV CNS disease, CSF levels of 14-3-3 protein were measured by quantitative immunoblotting throughout infection in 6 SIV-infected pigtailed macaques. Beginning during asymptomatic infection and continuing until death, CSF levels of 14-3-3 were elevated in 4 of 6 SIV-infected animals. Animals with 14-3-3 protein in CSF had the highest viral loads in the CSF after acute infection and the highest levels of both viral RNA and protein in brain (p < 0.001). In contrast, the presence of 14-3-3 protein in CSF was not associated with CNS microglial/macrophage activation measured by quantitative immunohistochemical staining for CD68 (p = 0.13). CSF levels of 14-3-3 protein may be a valuable marker of early neuronal damage, CNS viral replication, and CNS disease progression in HIV-infected individuals.
引用
收藏
页码:202 / 208
页数:7
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