Vehmas Ari, Lieu James, Pardo Carlos A, McArthur Justin C, Gartner Suzanne
Department of Neurology, Johns Hopkins Hospital, 600 North Wolfe Street, Baltimore, MD 21287, USA.
J Neuroimmunol. 2004 Dec;157(1-2):99-110. doi: 10.1016/j.jneuroim.2004.08.035.
We examined amyloid precursor protein (APP) surface expression on circulating leukocytes and in brain tissues from normal individuals and HIV+ subjects with cognitive impairment. Most monocytes, and a subset of B-lymphocytes, expressed APP, while T-lymphocytes, granulocytes, and natural killer (NK) cells did not. CD14bright/CD16+ monocytes expressed the highest levels, and CD14dim/CD16+ cells were negative, suggesting a relationship with activation. Higher APP+ monocyte levels correlated with increased numbers of CD16+ monocytes, but not with the degree of cognitive impairment. Treatment of monocytes with M-CSF, but not LPS, upregulated APP expression. In the brain, APP appeared as axonal immunoreactivity and diffuse plaques, and APP+ perivascular macrophages were seen in cases with severe dementia. APP may facilitate monocyte entry into the brain.
我们检测了正常个体以及患有认知障碍的HIV阳性受试者循环白细胞和脑组织中淀粉样前体蛋白(APP)的表面表达情况。大多数单核细胞以及一部分B淋巴细胞表达APP,而T淋巴细胞、粒细胞和自然杀伤(NK)细胞则不表达。CD14bright/CD16+单核细胞表达水平最高,而CD14dim/CD16+细胞呈阴性,提示与激活有关。较高的APP+单核细胞水平与CD16+单核细胞数量增加相关,但与认知障碍程度无关。用M-CSF而非LPS处理单核细胞会上调APP表达。在大脑中,APP表现为轴突免疫反应性和弥漫性斑块,在严重痴呆病例中可见APP+血管周围巨噬细胞。APP可能促进单核细胞进入大脑。