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核因子-κB结合位点对于猕猴猿猴免疫缺陷病毒在原代巨噬细胞中高效复制是必需的,但在体外对T细胞则并非如此。

The NF-kappa B binding site is necessary for efficient replication of simian immunodeficiency virus of macaques in primary macrophages but not in T cells in vitro.

作者信息

Bellas R E, Hopkins N, Li Y

机构信息

Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

J Virol. 1993 May;67(5):2908-13. doi: 10.1128/JVI.67.5.2908-2913.1993.

DOI:10.1128/JVI.67.5.2908-2913.1993
PMID:8474179
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC237617/
Abstract

We demonstrate here that the nuclear factor-kappa B (NF-kappa B) binding site in the simian immunodeficiency virus (SIVmac) long terminal repeat is essential for efficient virus replication in primary alveolar macrophages but dispensable for efficient replication in primary T cells. Mutation of the NF-kappa B site does not seriously impair replication of a T-cell-tropic SIVmac239 or a macrophagetropic SIVmacEm* in peripheral blood lymphocytes or established CD4+ cell lines; however, mutation of the NF-kappa B site prevents efficient SIVmacEm* replication in primary alveolar macrophages. These data suggest that efficient replication in primary macrophages requires both envelope and long terminal repeat determinants.

摘要

我们在此证明,猿猴免疫缺陷病毒(SIVmac)长末端重复序列中的核因子-κB(NF-κB)结合位点对于原代肺泡巨噬细胞中的高效病毒复制至关重要,但对于原代T细胞中的高效复制则是可有可无的。NF-κB位点的突变不会严重损害T细胞嗜性的SIVmac239或巨噬细胞嗜性的SIVmacEm在外周血淋巴细胞或已建立的CD4+细胞系中的复制;然而,NF-κB位点的突变会阻止SIVmacEm在原代肺泡巨噬细胞中的高效复制。这些数据表明,在原代巨噬细胞中的高效复制需要包膜和长末端重复序列决定簇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/237617/dab9da08000a/jvirol00026-0495-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/237617/26b4c7a1957b/jvirol00026-0493-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/237617/dab9da08000a/jvirol00026-0495-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/237617/26b4c7a1957b/jvirol00026-0493-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/237617/dab9da08000a/jvirol00026-0495-a.jpg

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