Expression of the Mannose Receptor CD206 in HIV and SIV Encephalitis: A Phenotypic Switch of Brain Perivascular Macrophages with Virus Infection

被引:38
|
作者
Holder, Gerard E. [1 ]
McGary, Christopher M. [1 ]
Johnson, Edward M. [1 ]
Zheng, Rubo [2 ]
John, Vijay T. [2 ]
Sugimoto, Chie [3 ]
Kuroda, Marcelo J. [3 ]
Kim, Woong-Ki [1 ]
机构
[1] Eastern Virginia Med Sch, Dept Microbiol & Mol Cell Biol, Norfolk, VA 23507 USA
[2] Tulane Univ, Dept Chem & Biomed Engn, New Orleans, LA 70118 USA
[3] Tulane Natl Primate Res Ctr, Div Immunol, Covington, LA 70433 USA
关键词
AIDS; Bisphosphonate liposome; Bromodeoxyuridine; HIV encephalitis; Macrophage; CENTRAL-NERVOUS-SYSTEM; MENINGEAL MACROPHAGES; LOCAL PROLIFERATION; NONHUMAN PRIMATE; DOWN-REGULATION; IN-VIVO; MONOCYTES; ALENDRONATE; BLOOD; ATHEROSCLEROSIS;
D O I
10.1007/s11481-014-9564-y
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We examined the expression of the mannose receptor CD206 by perivascular macrophages (PVM) in normal human and monkey brains and in brains of HIV-infected humans and of monkeys infected with simian immunodeficiency virus (SIV). Depletion of brain PVM in SIV-infected monkeys by intrathecal injection of liposome-encapsulated bisphosphonates eliminated CD206-expressing cells in the brain, confirming their perivascular location and phagocytic capacity. In vivo labeling with bromodeoxyuridine in normal uninfected and SIV-infected macaques in combination with CD206 immunostaining revealed a CD206+-to-CD206- shift within pre-existing PVM during SIV brain infection and neuroinflammation. These findings identify CD206 as a unique marker of human and macaque PVM, and underscore the utility of this marker in studying the origin, turnover and functions of these cells in AIDS.
引用
收藏
页码:716 / 726
页数:11
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