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猿猴免疫缺陷病毒脑炎中周围苯二氮䓬受体表达升高

Elevated peripheral benzodiazepine receptor expression in simian immunodeficiency virus encephalitis.

作者信息

Mankowski Joseph L, Queen Suzanne E, Tarwater Patrick J, Adams Robert J, Guilarte Tomas R

机构信息

Department of Comparative Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

出版信息

J Neurovirol. 2003 Feb;9(1):94-100. doi: 10.1080/13550280390173283.

Abstract

Measurement of central nervous system (CNS) expression of the peripheral benzodiazepine receptor (PBR), a microglia and macrophage activation marker, by positron emission tomography (PET) would aid clinical management of human immunodeficiency virus (HIV)-infected patients. To evaluate the utility of examining PBR expression in the CNS as a cellular activation marker in HIV CNS disease, PBR levels were measured in frontal cortex of simian immunodeficiency virus (SIV)-infected macaques with encephalitis and uninfected animals via PK11195 ligand autoradiography. [(3)H]-(R)-PK11195 binding to both grey matter (P =.017) and white matter (P =.038) was significantly higher in animals with SIV encephalitis (n = 10) versus control animals (n = 3). When PK11195 binding was compared with other microglial/macrophage activation markers (obtained via quantitative image analysis), a strong, significant association was found for both HAM56 (P =.004) and KP-1 (anti-CD68; P =.006) immunostaining in white matter. In contrast, grey matter PK11195 binding did not correlate with HAM56 (P =.46), KP-1 (P =.06), or glial fibrillary acidic protein (GFAP) immunostaining for astrocytic activation (P =.09). The regional nature of these increases in activation within the brain illustrates the crucial need to focus functional neuroimaging analyses of HIV-infected individuals on subcortical white matter to assess activation of microglia and macrophages.

摘要

通过正电子发射断层扫描(PET)测量外周苯二氮䓬受体(PBR,一种小胶质细胞和巨噬细胞激活标志物)在中枢神经系统(CNS)中的表达,将有助于对人类免疫缺陷病毒(HIV)感染患者进行临床管理。为了评估检测中枢神经系统中PBR表达作为HIV中枢神经系统疾病细胞激活标志物的效用,通过PK11195配体放射自显影术,测量了患有脑炎的猴免疫缺陷病毒(SIV)感染猕猴和未感染动物额叶皮质中的PBR水平。与对照动物(n = 3)相比,患有SIV脑炎的动物(n = 10)中,[(3)H]-(R)-PK11195与灰质(P =.017)和白质(P =.038)的结合均显著更高。当将PK11195结合与其他小胶质细胞/巨噬细胞激活标志物(通过定量图像分析获得)进行比较时,发现白质中HAM56(P =.004)和KP-1(抗CD68;P =.006)免疫染色均存在强且显著的相关性。相比之下,灰质PK11195结合与HAM56(P =.46)、KP-1(P =.06)或用于星形细胞激活的胶质纤维酸性蛋白(GFAP)免疫染色(P =.09)均无相关性。大脑内这些激活增加的区域特性表明,至关重要的是将对HIV感染个体的功能神经影像学分析聚焦于皮质下白质,以评估小胶质细胞和巨噬细胞的激活情况。

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