Sulforaphane Inhibits HIV Infection of Macrophages through Nrf2.
Marburg virus, the Kaposi's sarcoma-associated herpesvirus (KSHV) and Dengue virus all activate, and benefit from, expression of the transcription regulator nuclear erythroid 2-related factor 2 (Nrf2). The impact of Nrf2 activation on human immunodeficiency virus (HIV) infection has not been te...
Main Authors: | , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2016-04-01
|
Series: | PLoS Pathogens |
Online Access: | http://europepmc.org/articles/PMC4836681?pdf=render |
id |
doaj-f655d1b535d045bfa5255a5f02ae1ae6 |
---|---|
record_format |
Article |
spelling |
doaj-f655d1b535d045bfa5255a5f02ae1ae62020-11-25T02:20:16ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742016-04-01124e100558110.1371/journal.ppat.1005581Sulforaphane Inhibits HIV Infection of Macrophages through Nrf2.Andrea Kinga Marias FuruyaHamayun J SharifiRobert M JellingerPaul CristofanoBinshan ShiCarlos M C de NoronhaMarburg virus, the Kaposi's sarcoma-associated herpesvirus (KSHV) and Dengue virus all activate, and benefit from, expression of the transcription regulator nuclear erythroid 2-related factor 2 (Nrf2). The impact of Nrf2 activation on human immunodeficiency virus (HIV) infection has not been tested. Sulforaphane (SFN), produced in cruciferous vegetables after mechanical damage, mobilizes Nrf2 to potently reprogram cellular gene expression. Here we show for the first time that SFN blocks HIV infection in primary macrophages but not in primary T cells. Similarly SFN blocks infection in PMA-differentiated promonocytic cell lines, but not in other cell lines tested. siRNA-mediated depletion of Nrf2 boosted HIV infectivity in primary macrophages and reduced the anti-viral effects of SFN treatment. This supports a model in which anti-viral activity is mediated through Nrf2 after it is mobilized by SFN. We further found that, like the type I interferon-induced cellular anti-viral proteins SAMHD1 and MX2, SFN treatment blocks infection after entry, but before formation of 2-LTR circles. Interestingly however, neither SAMHD1 nor MX2 were upregulated. This shows for the first time that Nrf2 action can potently block HIV infection and highlights a novel way to trigger this inhibition.http://europepmc.org/articles/PMC4836681?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Andrea Kinga Marias Furuya Hamayun J Sharifi Robert M Jellinger Paul Cristofano Binshan Shi Carlos M C de Noronha |
spellingShingle |
Andrea Kinga Marias Furuya Hamayun J Sharifi Robert M Jellinger Paul Cristofano Binshan Shi Carlos M C de Noronha Sulforaphane Inhibits HIV Infection of Macrophages through Nrf2. PLoS Pathogens |
author_facet |
Andrea Kinga Marias Furuya Hamayun J Sharifi Robert M Jellinger Paul Cristofano Binshan Shi Carlos M C de Noronha |
author_sort |
Andrea Kinga Marias Furuya |
title |
Sulforaphane Inhibits HIV Infection of Macrophages through Nrf2. |
title_short |
Sulforaphane Inhibits HIV Infection of Macrophages through Nrf2. |
title_full |
Sulforaphane Inhibits HIV Infection of Macrophages through Nrf2. |
title_fullStr |
Sulforaphane Inhibits HIV Infection of Macrophages through Nrf2. |
title_full_unstemmed |
Sulforaphane Inhibits HIV Infection of Macrophages through Nrf2. |
title_sort |
sulforaphane inhibits hiv infection of macrophages through nrf2. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Pathogens |
issn |
1553-7366 1553-7374 |
publishDate |
2016-04-01 |
description |
Marburg virus, the Kaposi's sarcoma-associated herpesvirus (KSHV) and Dengue virus all activate, and benefit from, expression of the transcription regulator nuclear erythroid 2-related factor 2 (Nrf2). The impact of Nrf2 activation on human immunodeficiency virus (HIV) infection has not been tested. Sulforaphane (SFN), produced in cruciferous vegetables after mechanical damage, mobilizes Nrf2 to potently reprogram cellular gene expression. Here we show for the first time that SFN blocks HIV infection in primary macrophages but not in primary T cells. Similarly SFN blocks infection in PMA-differentiated promonocytic cell lines, but not in other cell lines tested. siRNA-mediated depletion of Nrf2 boosted HIV infectivity in primary macrophages and reduced the anti-viral effects of SFN treatment. This supports a model in which anti-viral activity is mediated through Nrf2 after it is mobilized by SFN. We further found that, like the type I interferon-induced cellular anti-viral proteins SAMHD1 and MX2, SFN treatment blocks infection after entry, but before formation of 2-LTR circles. Interestingly however, neither SAMHD1 nor MX2 were upregulated. This shows for the first time that Nrf2 action can potently block HIV infection and highlights a novel way to trigger this inhibition. |
url |
http://europepmc.org/articles/PMC4836681?pdf=render |
work_keys_str_mv |
AT andreakingamariasfuruya sulforaphaneinhibitshivinfectionofmacrophagesthroughnrf2 AT hamayunjsharifi sulforaphaneinhibitshivinfectionofmacrophagesthroughnrf2 AT robertmjellinger sulforaphaneinhibitshivinfectionofmacrophagesthroughnrf2 AT paulcristofano sulforaphaneinhibitshivinfectionofmacrophagesthroughnrf2 AT binshanshi sulforaphaneinhibitshivinfectionofmacrophagesthroughnrf2 AT carlosmcdenoronha sulforaphaneinhibitshivinfectionofmacrophagesthroughnrf2 |
_version_ |
1724872437137408000 |