Lentivirus infection of macrophages.

Immunology series Pub Date : 1994-01-01
J E Clements, M C Zink, O Narayan, D H Gabuzda
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Abstract

The ovine and caprine lentiviruses infect monocytes, and the viral DNA is integrated into the cellular DNA. The provirus remains silent until the monocyte matures into a macrophage. Intrinsic to this maturation is the induction of a class of immediate early genes in the monocyte that includes the transcription factors JUN and FOS. These transcription factors are thought to couple short-term signals in the cell to long-term cellular differentiation by regulation of specific cellular genes. Thus, JUN and FOS bind to the AP-1 site in the promoters of cellular genes and activate their transcription, resulting in maturation of the monocyte into a macrophage. In addition, these cellular factors activate the same AP-1 sequence in the visna virus LTR, leading to transcriptional activation, full viral gene expression, and production of progeny virus. The expression of viral antigens in the context of MHC class II on the macrophage leads to the production of cytokines and a lymphoproliferative response that causes the lesions in specific target organs in an infected animal. We still understand only the framework of these events. The specific mechanisms by which viral genes alter macrophage gene expression and the molecular basis of different viral tropism for specific tissue macrophages, i.e. microglia, remain to be determined.

慢病毒感染巨噬细胞。
绵羊和山羊慢病毒感染单核细胞,病毒DNA被整合到细胞DNA中。在单核细胞成熟为巨噬细胞之前,原病毒保持沉默。这种成熟的内在是在单核细胞中诱导一类直接早期基因,包括转录因子JUN和FOS。这些转录因子被认为通过调节特定的细胞基因,将细胞中的短期信号与长期细胞分化结合起来。因此,JUN和FOS结合到细胞基因启动子的AP-1位点并激活其转录,导致单核细胞成熟为巨噬细胞。此外,这些细胞因子激活了visna病毒LTR中相同的AP-1序列,导致转录激活、病毒基因的完全表达和子代病毒的产生。在MHC II类背景下,巨噬细胞上病毒抗原的表达导致细胞因子的产生和淋巴细胞增殖反应,导致受感染动物的特定靶器官病变。我们仍然只了解这些事件的框架。病毒基因改变巨噬细胞基因表达的具体机制以及特定组织巨噬细胞(如小胶质细胞)不同病毒趋向性的分子基础仍有待确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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