Venneti Sriram, Wang Guoji, Wiley Clayton A
Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Neurobiol Dis. 2008 Feb;29(2):232-41. doi: 10.1016/j.nbd.2007.08.016. Epub 2007 Sep 7.
HIV encephalitis (HIVE) is characterized by neurodegeneration mediated by toxins derived from infected and activated brain macrophages. Since the peripheral benzodiazepine receptor (PBR) is abundant on brain macrophages, we hypothesized that [(3)H]DAA1106, a new PBR ligand, can label infected and activated brain macrophages in HIVE. Using cell culture and postmortem brain tissues from HIVE and a macaque model of HIVE, we show that [(3)H]DAA1106 binds with high affinity to activated and infected macrophages in regions of synaptic damage. Further, binding affinity reflected by lower K(D) (dissociation constant) values and the B(max) (total number of binding sites) to K(D) ratios reflective of ligand-binding potential was significantly higher with [(3)H]DAA1106 compared to the extensively characterized PBR ligand (3)H-PK11195. These data suggest that DAA1106 binds with high affinity to activated and infected brain macrophages and possesses binding characteristics beneficial for in vivo use in the detection and clinical monitoring of HIVE using positron emission tomography.
HIV 脑炎(HIVE)的特征是由受感染并被激活的脑巨噬细胞产生的毒素介导的神经退行性变。由于外周苯二氮䓬受体(PBR)在脑巨噬细胞上大量存在,我们推测新型 PBR 配体[(3)H]DAA1106 能够标记 HIVE 中受感染并被激活的脑巨噬细胞。利用来自 HIVE 的细胞培养物和尸检脑组织以及 HIVE 的猕猴模型,我们发现[(3)H]DAA1106 与突触损伤区域中被激活并受感染的巨噬细胞具有高亲和力结合。此外,与广泛研究的 PBR 配体(3)H-PK11195 相比,[(3)H]DAA1106 的较低解离常数(K(D))值以及反映配体结合潜力的 B(max)(结合位点总数)与 K(D) 之比所反映的结合亲和力显著更高。这些数据表明 DAA1106 与被激活并受感染的脑巨噬细胞具有高亲和力结合,并且具有有利于在正电子发射断层扫描中用于 HIVE 的检测和临床监测的结合特性。