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The ability of SAMHD1 to block HIV-1 but not SIV requires expression of MxB.
Buffone, Cindy; Kutzner, Juliane; Opp, Silvana; Martinez-Lopez, Alicia; Selyutina, Anastasia; Coggings, Si Ana; Studdard, Lydia R; Ding, Lingmei; Kim, Baek; Spearman, Paul; Schaller, Torsten; Diaz-Griffero, Felipe.
Afiliação
  • Buffone C; Albert Einstein College of Medicine, Microbiology and Immunology, Bronx, NY, 10461, USA.
  • Kutzner J; University Hospital Heidelberg, Department of Infectious Diseases, Heidelberg, 69120, Germany.
  • Opp S; Albert Einstein College of Medicine, Microbiology and Immunology, Bronx, NY, 10461, USA.
  • Martinez-Lopez A; Albert Einstein College of Medicine, Microbiology and Immunology, Bronx, NY, 10461, USA.
  • Selyutina A; Albert Einstein College of Medicine, Microbiology and Immunology, Bronx, NY, 10461, USA.
  • Coggings SA; Emory University, Pediatrics, Atlanta, 30322, Georgia.
  • Studdard LR; Emory University, Pediatrics, Atlanta, 30322, Georgia.
  • Ding L; Cincinnati Children's Hospital, Infectious Diseases, Cincinnati, OH, 45229, USA.
  • Kim B; Emory University, Pediatrics, Atlanta, 30322, Georgia.
  • Spearman P; Cincinnati Children's Hospital, Infectious Diseases, Cincinnati, OH, 45229, USA.
  • Schaller T; University Hospital Heidelberg, Department of Infectious Diseases, Heidelberg, 69120, Germany.
  • Diaz-Griffero F; Albert Einstein College of Medicine, Microbiology and Immunology, Bronx, NY, 10461, USA. Electronic address: felipe.diaz-griffero@einstein.yu.edu.
Virology ; 531: 260-268, 2019 05.
Article em En | MEDLINE | ID: mdl-30959264
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article