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本文引用的文献

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Innate immune responses to cytomegalovirus infection in the developing mouse brain and their evasion by virus-infected neurons.发育中小鼠大脑对巨细胞病毒感染的先天性免疫反应以及病毒感染神经元对其的逃避。
Am J Pathol. 2002 Sep;161(3):919-28. doi: 10.1016/S0002-9440(10)64252-6.
2
Neurons differentially activate the herpes simplex virus type 1 immediate-early gene ICP0 and ICP27 promoters in transgenic mice.在转基因小鼠中,神经元对单纯疱疹病毒1型立即早期基因ICP0和ICP27启动子有不同程度的激活作用。
J Virol. 2002 Mar;76(5):2449-59. doi: 10.1128/jvi.76.5.2449-2459.2002.
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Activation of murine cytomegalovirus immediate-early promoter in cerebral ventricular zone and glial progenitor cells in transgenic mice.小鼠巨细胞病毒立即早期启动子在转基因小鼠脑室区和神经胶质祖细胞中的激活。
Glia. 2001 Jul;35(1):41-52. doi: 10.1002/glia.1069.
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Detection of cytomegalovirus DNA in human specimens by LightCycler PCR.运用LightCycler PCR技术检测人类样本中的巨细胞病毒DNA。
J Clin Microbiol. 2000 Nov;38(11):4006-9. doi: 10.1128/JCM.38.11.4006-4009.2000.
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Growth retardation and microcephaly induced in mice by placental infection with murine cytomegalovirus.小鼠巨细胞病毒胎盘感染诱导小鼠生长迟缓和小头畸形。
Teratology. 2000 Aug;62(2):79-85. doi: 10.1002/1096-9926(200008)62:2<79::AID-TERA3>3.0.CO;2-S.
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Cytomegalovirus cell tropism, replication, and gene transfer in brain.巨细胞病毒在脑内的细胞嗜性、复制及基因转移
J Neurosci. 1999 Dec 15;19(24):10948-65. doi: 10.1523/JNEUROSCI.19-24-10948.1999.
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Murine cytomegalovirus immediate-early promoter directs astrocyte-specific expression in transgenic mice.鼠巨细胞病毒立即早期启动子在转基因小鼠中指导星形胶质细胞特异性表达。
Am J Pathol. 1999 Mar;154(3):735-43. doi: 10.1016/S0002-9440(10)65320-5.
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Murine cytomegalovirus induces apoptosis in non-infected cells of the developing mouse brain and blocks apoptosis in primary neuronal culture.
Acta Neuropathol. 1998 Sep;96(3):239-47. doi: 10.1007/s004010050890.
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Cytomegalovirus infections of the nervous system.
Intervirology. 1997;40(2-3):85-97. doi: 10.1159/000150536.
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Differential expression of the immediate-early and early antigens in neuronal and glial cells of developing mouse brains infected with murine cytomegalovirus.感染鼠巨细胞病毒的发育中小鼠脑神经元和神经胶质细胞中即刻早期抗原和早期抗原的差异表达。
Am J Pathol. 1997 Nov;151(5):1331-40.

转基因小鼠中鼠巨细胞病毒早期基因e1启动子的神经元特异性激活。

Neuron-specific activation of murine cytomegalovirus early gene e1 promoter in transgenic mice.

作者信息

Arai Yoshifumi, Ishiwata Mizuho, Baba Satoshi, Kawasaki Hideya, Kosugi Isao, Li Ren-Yong, Tsuchida Takashi, Miura Katsutoshi, Tsutsui Yoshihiro

机构信息

Department of Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan.

出版信息

Am J Pathol. 2003 Aug;163(2):643-52. doi: 10.1016/S0002-9440(10)63691-7.

DOI:10.1016/S0002-9440(10)63691-7
PMID:12875983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1868196/
Abstract

The brain is the main target in congenital cytomegalovirus (CMV) infection and immunocompromised patients. No definite evidence that a CMV has special affinity for the central nervous system (CNS) has been published. Here, we generated transgenic mice with an e1 promoter/enhancer region connected to the reporter gene lacZ. Surprisingly, expression of the transgene was completely restricted to the CNS in all lines of transgenic mice. The transgene was expressed in subpopulation of neurons in the cerebral cortex, hippocampus, diencephalon, brainstem, cerebellum, and spinal cord in all of the lines. Non-neuronal cells in the CNS were negative for transgene expression. Activation of the transgene was first observed in neurons of mesencephalon in late gestation, and then the number of positive neurons increased in various parts of the brain as development proceeded. Upon infection of the transgenic mouse brains with MCMV, the location of the activated neurons became more extensive, and the number of such neurons increased. These results suggest that there are host factor(s) that directly activate the MCMV early gene promoter in neurons. This neuron-specific activation may be associated with persistent infection in the brain and may be responsible for the neuronal dysfunction and neuronal cell loss caused by CMV infection.

摘要

大脑是先天性巨细胞病毒(CMV)感染和免疫功能低下患者的主要靶器官。目前尚无明确证据表明CMV对中枢神经系统(CNS)具有特殊亲和力。在此,我们构建了将e1启动子/增强子区域与报告基因lacZ相连的转基因小鼠。令人惊讶的是,在所有转基因小鼠品系中,转基因的表达完全局限于中枢神经系统。在所有品系中,转基因在大脑皮层、海马体、间脑、脑干、小脑和脊髓的神经元亚群中表达。中枢神经系统中的非神经元细胞转基因表达呈阴性。转基因的激活在妊娠后期首先在中脑神经元中观察到,然后随着发育的进行,大脑各部位阳性神经元的数量增加。用MCMV感染转基因小鼠大脑后,被激活神经元的位置变得更加广泛,且此类神经元的数量增加。这些结果表明,存在直接激活神经元中MCMV早期基因启动子的宿主因子。这种神经元特异性激活可能与大脑中的持续感染有关,并且可能是CMV感染导致神经元功能障碍和神经元细胞丢失的原因。