Bermudez L E, Goodman J, Petrofsky M
Kuzell Institute for Arthritis and Infectious Diseases, California Pacific Medical Center Research Institute, San Francisco, California 94115, USA.
Infect Immun. 1999 Sep;67(9):4912-6. doi: 10.1128/IAI.67.9.4912-4916.1999.
Mycobacterium avium is an intracellular pathogen that has been shown to invade macrophages by using complement receptors in vitro, but mycobacteria released from one cell can enter a second macrophage by using receptors different from complement receptors. Infection of CD18 (beta(2) integrin) knockout mice and the C57 BL/6 control mice led to comparable levels of tissue infection at 1 day, 2 days, 1 week, and 3 weeks following administration of bacteria. A histopathological study revealed similar granulomatous lesions in the two mouse strains, with comparable numbers of organisms. In addition, transmission electron microscopy of spleen tissues from both strains of mice showed bacteria inside macrophages. Our in vivo findings support the hypothesis that M. avium in the host is likely to use receptors other than CR3 and CR4 receptors to enter macrophages with increased efficiency.
鸟分枝杆菌是一种细胞内病原体,已证明其在体外通过利用补体受体侵入巨噬细胞,但从一个细胞释放的分枝杆菌可通过使用不同于补体受体的受体进入第二个巨噬细胞。给CD18(β2整合素)基因敲除小鼠和C57 BL/6对照小鼠接种细菌后1天、2天、1周和3周,组织感染水平相当。组织病理学研究显示,这两种小鼠品系中存在相似的肉芽肿性病变,病原体数量相当。此外,对两种小鼠品系的脾脏组织进行透射电子显微镜检查,均显示巨噬细胞内有细菌。我们的体内研究结果支持这样一种假说,即宿主体内的鸟分枝杆菌可能利用CR3和CR4受体以外的受体更有效地进入巨噬细胞。