Immunohistochemical evidence for a macrophage scavenger receptor in mate cells and reactive microglia of ischemia and Alzheimer's disease

被引:45
作者
Honda, M [1 ]
Akiyama, H
Yamada, Y
Kondo, H
Kawabe, Y
Takeya, M
Takahashi, K
Suzuki, H
Doi, T
Sakamoto, A
Ookawara, S
Mato, M
Gough, PJ
Greaves, DR
Gordon, S
Kodama, T
Matsushita, M
机构
[1] Univ Tokyo, Dept Neuropsychiat, Tokyo 113, Japan
[2] Tokyo Inst Psychiat, Tokyo 156, Japan
[3] Univ Tokyo, Adv Sci & Technol Res Ctr, Tokyo 153, Japan
[4] Osaka Univ, Fac Pharmaceut Sci, Suita, Osaka 565, Japan
[5] Kumamoto Univ, Dept Pathol, Kumamoto 860, Japan
[6] Jichi Med Sch, Dept Anat, Minami Kawachi, Tochigi 32904, Japan
[7] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
关键词
macrophage scavenger receptor; gene-deficient mouse; monoclonal antibody; atherosclerosis; Mato's fluorescent granular perithelial cell (Mato cell); microglia; Alzheimer's disease; ischemia;
D O I
10.1006/bbrc.1998.8120
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macrophage scavenger receptors (MSR) are implicated in the development of atherosclerosis and amyloid b-protein deposition in Alzheimer's disease. However, histopathological studies of MSR expression in human tissues have been hampered by a lack of specific antibodies. Using MSR-deficient mice, we successfully raised a novel monoclonal antibody against human MSR together with high-titer antisera. These antibodies specifically recognized human tissue macrophages and human MSR protein purified from differentiated THP1 cells. In normal brain, MSR staining was mainly distributed to the perivascular cells, which correspond to Mate's fluorescent granular perithelial cells (Mato cells). In the lesions of ischemia and Alzheimer's disease, a subset of microglia stained positive for MSR. These novel antibodies are useful tools for analysis of MSR expression in human tissues. (C) 1998 Academic Press.
引用
收藏
页码:734 / 740
页数:7
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