Albert Einstein College of Medicine, Microbiology and Immunology, Bronx, NY, 10461, USA.
University Hospital Heidelberg, Department of Infectious Diseases, Heidelberg, 69120, Germany.
Virology. 2019 May;531:260-268. doi: 10.1016/j.virol.2019.03.018. Epub 2019 Mar 30.
SAMHD1 is a human restriction factor known to prevent infection of macrophages, resting CD4 T cells, and dendritic cells by HIV-1. To test the contribution of MxB to the ability of SAMHD1 to block HIV-1 infection, we created human THP-1 cell lines that were knocked out for expression of MxB, SAMHD1, or both. Interestingly, MxB depletion renders SAMHD1 ineffective against HIV-1 but not SIVmac. We observed similar results in human primary macrophages that were knockdown for the expression of MxB. To understand how MxB assists SAMHD1 restriction of HIV-1, we examined direct interaction between SAMHD1 and MxB in pull-down experiments. In addition, we investigated several properties of SAMHD1 in the absence of MxB expression, including subcellular localization, phosphorylation of the SAMHD1 residue T592, and dNTPs levels. These experiments showed that SAMHD1 restriction of HIV-1 requires expression of MxB.
SAMHD1 是一种已知的人类限制因子,可防止 HIV-1 感染巨噬细胞、静止的 CD4 T 细胞和树突状细胞。为了测试 MxB 对 SAMHD1 阻断 HIV-1 感染能力的贡献,我们创建了敲除 MxB、SAMHD1 或两者的人 THP-1 细胞系。有趣的是,MxB 耗尽使 SAMHD1 对 HIV-1 无效,但对 SIVmac 有效。我们在敲低 MxB 表达的人原代巨噬细胞中观察到了类似的结果。为了了解 MxB 如何协助 SAMHD1 限制 HIV-1,我们在下拉实验中检查了 SAMHD1 和 MxB 之间的直接相互作用。此外,我们还研究了缺乏 MxB 表达时 SAMHD1 的几个特性,包括亚细胞定位、SAMHD1 残基 T592 的磷酸化和 dNTPs 水平。这些实验表明,SAMHD1 对 HIV-1 的限制需要 MxB 的表达。