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从一例热带痉挛性截瘫患者分离出的人嗜T淋巴细胞病毒I型(HTLV-I)前病毒的长末端重复序列(LTR)在转基因小鼠中指导的组织表达模式。

Tissue expression pattern directed in transgenic mice by the LTR of an HTLV-I provirus isolated from a case of tropical spastic paraparesis.

作者信息

Gonzalez-Dunia D, Grimber G, Briand P, Brahic M, Ozden S

机构信息

Département des Rétrovirus, UA CNRS 1157, Institut Pasteur, Paris, France.

出版信息

Virology. 1992 Apr;187(2):705-10. doi: 10.1016/0042-6822(92)90473-3.

Abstract

Human T lymphotropic virus type I (HTLV-I) causes adult T cell leukemia/lymphoma and a chronic neurological disease called either tropical spastic paraparesis (TSP) or HTLV-I-associated myelopathy. The different outcomes of this infection could be due to both host and viral factors and it has been proposed that genetic differences could make some HTLV-I strains neurotropic. In this paper, we examined the pattern of tissue-specific expression determined by a long terminal repeat (LTR) obtained from a case of TSP. We constructed transgenic mice in which this LTR controlled the expression of the nlslacZ reporter gene. We observed that in three independent lines of transgenic mice, the reporter gene was expressed predominantly in the central nervous system (CNS), in choroid plexus, and in cells of the hippocampus and cerebellum. Our observations indicate the existence of CNS cells permissive for the expression of HTLV-I and which may be of importance in the pathogenesis of TSP.

摘要

人类嗜T淋巴细胞病毒I型(HTLV-I)可引发成人T细胞白血病/淋巴瘤以及一种名为热带痉挛性截瘫(TSP)或HTLV-I相关脊髓病的慢性神经疾病。这种感染产生不同结果可能归因于宿主和病毒因素,并且有人提出基因差异可能使某些HTLV-I毒株具有嗜神经性。在本文中,我们研究了从一例TSP病例中获得的长末端重复序列(LTR)所决定的组织特异性表达模式。我们构建了转基因小鼠,其中该LTR控制nls1lacZ报告基因的表达。我们观察到,在三个独立的转基因小鼠品系中,报告基因主要在中枢神经系统(CNS)、脉络丛以及海马体和小脑的细胞中表达。我们的观察结果表明存在允许HTLV-I表达的CNS细胞,这可能在TSP的发病机制中具有重要意义。

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