首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Analysis of thymic endogenous retroviral expression in murine lupus. Genetic and immune studies.
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Analysis of thymic endogenous retroviral expression in murine lupus. Genetic and immune studies.

机译:胸腺内源性逆转录病毒在小鼠狼疮中的表达分析。遗传和免疫研究。

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摘要

Inbred mouse genomes contain two subclasses of proviruses related to mink cell focus-forming (MCF) retroviruses: polytropic (Pmv), and modified polytropic (Mpmv). To determine whether one of these subclasses is associated with murine lupus, oligonucleotide probes specific for Pmv or Mpmv sequences were used in Northern analyses. Thymus 8.4 kb Mpmv RNA was expressed in five of five lupus-prone strains and crosses and this expression was not affected by genes that retard or accelerate development of lupus. Two of four leukemia-prone strains expressed low levels of such thymic transcripts, but none of 11 control strains did. 8.4 kb Mpmv RNA expression was not induced in thymuses of control mice by the lpr/lpr or gld/gld genotypes (which cause polyclonal immune activation) nor by treatment with mitogens. In contrast to Mpmv, thymic 8.4 kb Pmv expression was poorly associated with autoimmunity: it was easily detected in nearly all strains, and was increased by polyclonal activation in control mice. These studies indicate that the organ-specific thymic 8.4 kb Mpmv expression (a) is characteristic of several genetic backgrounds which predispose to murine lupus, (b) precedes and does not correlate with disease development, (c) is not due to polyclonal activation, and (d) is regulated independently of 8.4 kb Pmv expression.
机译:近交小鼠基因组包含与貂细胞聚焦形成(MCF)逆转录病毒相关的前病毒的两个亚类:多变(Pmv)和修饰的多变(Mpmv)。为了确定这些亚类之一是否与鼠科狼疮有关,在Northern分析中使用了对Pmv或Mpmv序列特异的寡核苷酸探针。胸腺8.4 kb Mpmv RNA在5个易患狼疮的菌株和杂交物中的5个中表达,该表达不受延迟或加速狼疮发育的基因的影响。四个易患白血病的菌株中有两个表达低水平的胸腺转录本,但11个对照菌株中没有一个表达。 lpr / lpr或gld / gld基因型(引起多克隆免疫激活)或用促细胞分裂剂处理均未在对照小鼠的胸腺中诱导8.4 kb Mpmv RNA表达。与Mpmv相反,胸腺8.4 kb Pmv表达与自身免疫性相关性很弱:几乎在所有菌株中都易于检测到,并通过多克隆激活在对照小鼠中增加。这些研究表明,特定于器官的胸腺8.4 kb Mpmv表达(a)是几种遗传背景的特征,这些遗传背景易患鼠科狼疮;(b)在疾病发生之前且与疾病发展无关;(c)并非由于多克隆激活; (d)不受8.4 kb Pmv表达的调节。

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