MRI confirms loss of blood-brain barrier integrity in a mouse model of disseminated candidiasis

被引:26
|
作者
Navarathna, Dhammika H. M. L. P. [1 ]
Munasinghe, Jeeva [2 ]
Lizak, Martin J. [2 ]
Nayak, Debasis [2 ]
McGavern, Dorian B. [2 ]
Roberts, David D. [1 ]
机构
[1] NCI, Pathol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] NINDS, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Candida albicans; murine disseminated candidiasis; blood-brain barrier; MRI; extracellular vascular contrast agent Gd-DTPA; ultrasmall iron oxide particles; intravital two-photon microscopy; CENTRAL-NERVOUS-SYSTEM; USPIO-ENHANCED MR; IRON-OXIDE PARTICLES; INFECTIOUS OSTEOMYELITIS; CELL RECRUITMENT; ALBICANS; INFILTRATION; MACROPHAGES; LYMPHOCYTES; REJECTION;
D O I
10.1002/nbm.2926
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Disseminated candidiasis primarily targets the kidneys and brain in mice and humans. Damage to these critical organs leads to the high mortality associated with such infections, and invasion across the blood-brain barrier can result in fungal meningoencephalitis. Candida albicans can penetrate a brain endothelial cell barrier in vitro through transcellular migration, but this mechanism has not been confirmed in vivo. MRI using the extracellular vascular contrast agent gadolinium diethylenetriaminepentaacetic acid demonstrated that integrity of the blood-brain barrier is lost during C. albicans invasion. Intravital two-photon laser scanning microscopy was used to provide the first real-time demonstration of C. albicans colonizing the living brain, where both yeast and filamentous forms of the pathogen were found. Furthermore, we adapted a previously described method utilizing MRI to monitor inflammatory cell recruitment into infected tissues in mice. Macrophages and other phagocytes were visualized in kidney and brain by the administration of ultrasmall iron oxide particles. In addition to obtaining new insights into the passage of C. albicans across the brain microvasculature, these imaging methods provide useful tools to study further the pathogenesis of C. albicans infections, to define the roles of Candida virulence genes in kidney versus brain infection and to assess new therapeutic measures for drug development. Published 2013. This article is a U.S. Government work and is in the public domain in the USA.
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页码:1125 / 1134
页数:10
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