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来自HIV相关认知障碍患者的循环单核细胞和脑巨噬细胞中的淀粉样前体蛋白表达。

Amyloid precursor protein expression in circulating monocytes and brain macrophages from patients with HIV-associated cognitive impairment.

作者信息

Vehmas Ari, Lieu James, Pardo Carlos A, McArthur Justin C, Gartner Suzanne

机构信息

Department of Neurology, Johns Hopkins Hospital, 600 North Wolfe Street, Baltimore, MD 21287, USA.

出版信息

J Neuroimmunol. 2004 Dec;157(1-2):99-110. doi: 10.1016/j.jneuroim.2004.08.035.

Abstract

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.

摘要

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。

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