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用于分析发育性脑部疾病的脑片培养,特别提及先天性巨细胞病毒感染。

Brain slice culture for analysis of developmental brain disorders with special reference to congenital cytomegalovirus infection.

作者信息

Kawasaki Hideya, Tsutsui Yoshihiro

机构信息

Second Department of Pathology, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.

出版信息

Congenit Anom (Kyoto). 2003 Jun;43(2):105-13. doi: 10.1111/j.1741-4520.2003.tb01034.x.

Abstract

Cytomegalovirus (CMV) is the most significant infectious cause of congenital abnormalities of the central nervous system (CNS) with variation from the fatal cytomegalic inclusion disease to functional brain disorder. The phenotype and degree of the brain disorder depends on infection time during the developing stage, virulence, route of infection and the viral susceptibility of the cells. The pathogenesis of the CMV infection to the CNS seems to be strongly related to neural migration, neural death, cellular compositions and the immune system of the brain. To understand the complex mechanism of this disorder, we used organotypic brain slice cultures. In the brain slice culture system, migration of CMV-infected neuronal cells was observed, which reflects infectious dynamics in vivo. Neural progenitor cells or glial immature cells in the subventricular zone and marginal area are most susceptible to murine cytomegalovirus (MCMV) infection in this system. The susceptibility declined as the number of immature glial cells decreased with age. The immature glial cells proliferated in brain slice cultures during prolonged incubation, and the susceptibility to MCMV infection also increased in association with the proliferation of these cells. The brain slice from an immunocompromised mouse (Beige-SCID mouse) unexpectedly showed lower susceptibility than that of an immunocompetent mouse during any prolonged incubation. These results suggest that the number of immature glial cells might determine the susceptibility of CMV infection to the brain, independent of the immune system. We reviewed recent findings of CMV infection to the brain from the perspective of brain slice cultures and the possibility that this system could be a useful method to investigate mechanisms of congenital anomaly of the brain.

摘要

巨细胞病毒(CMV)是中枢神经系统(CNS)先天性异常最主要的感染性病因,其表现形式多样,从致命的巨细胞包涵体病到功能性脑障碍不等。脑部疾病的表型和程度取决于发育阶段的感染时间、病毒毒力、感染途径以及细胞对病毒的易感性。CMV感染中枢神经系统的发病机制似乎与神经迁移、神经死亡、细胞组成以及脑部免疫系统密切相关。为了了解这种疾病的复杂机制,我们使用了脑片器官培养。在脑片培养系统中,观察到了CMV感染的神经元细胞的迁移,这反映了体内的感染动态。在该系统中,脑室下区和边缘区的神经祖细胞或胶质未成熟细胞对鼠巨细胞病毒(MCMV)感染最为敏感。随着未成熟胶质细胞数量随年龄减少,易感性也随之下降。在长时间孵育过程中,未成熟胶质细胞在脑片培养物中增殖,并且对MCMV感染的易感性也随着这些细胞的增殖而增加。在任何长时间孵育过程中出现意外情况,免疫受损小鼠(米色-SCID小鼠)的脑片比免疫健全小鼠的脑片显示出更低的易感性。这些结果表明,未成熟胶质细胞的数量可能决定CMV感染脑部的易感性,而与免疫系统无关。我们从脑片培养的角度回顾了CMV感染脑部的最新研究结果,以及该系统可能成为研究脑先天性异常机制的有用方法的可能性。

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