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人类单核细胞和巨噬细胞的HIV1感染促进NF-κB相关因子的诱导或易位。

HIV1 infection of human monocytes and macrophages promotes induction or translocation of NF-KB-related factors.

作者信息

Neuveut C, Suzan M, Querat G, Sire J

机构信息

Laboratoire de Virologie, Faculté de Médecine Secteur Nord, Marseille, France.

出版信息

Res Virol. 1991 Mar-Jun;142(2-3):227-31. doi: 10.1016/0923-2516(91)90061-7.

Abstract

In 1991, we demonstrated, using electrophoretic mobility shift assays, that 3 different factors (termed B1, B2 and B3) with affinity for the KB-enhancer target sequence were specifically detected in nuclear extracts from HIV1-infected monocytes and macrophages. The B2 factor was induced in the nuclei of these cells only upon HIV1 infection. The B3 factor was only slightly evident in nuclei of uninfected cells but was readily detectable in nuclei of infected monocytes. Its expression remained very low in nuclei of HIV1-infected macrophages. In this paper, we demonstrate that the B2 factor is expressed in the cytosol of monocytes and macrophages as a DNA-binding protein, indicating that it is not associated with an inhibitor (IKB). This factor remained clustered in the cytosol and was translocated to the nuclei only after HIV1 infection. The B3 factor is detected in the cytosol only when cells are HIV1-infected. The role of HIV1 infection in the expression and the translocation of these factors is discussed.

摘要

1991年,我们通过电泳迁移率变动分析证明,在来自感染HIV-1的单核细胞和巨噬细胞的核提取物中,特异性检测到3种对KB增强子靶序列具有亲和力的不同因子(称为B1、B2和B3)。B2因子仅在HIV-1感染时在这些细胞的细胞核中被诱导。B3因子在未感染细胞的细胞核中仅略有显现,但在感染的单核细胞核中很容易检测到。其在感染HIV-1的巨噬细胞核中的表达仍然很低。在本文中,我们证明B2因子作为一种DNA结合蛋白在单核细胞和巨噬细胞的细胞质中表达,这表明它不与抑制剂(IκB)相关。该因子在细胞质中保持聚集状态,仅在HIV-1感染后才转移到细胞核中。B3因子仅在细胞被HIV-1感染时在细胞质中被检测到。本文讨论了HIV-1感染在这些因子的表达和转移中的作用。

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