Diverse roles of HDAC6 in viral infection: Implications for antiviral therapy

被引:20
作者
Zhang, Linlin [1 ]
Ogden, Angela [2 ]
Aneja, Ritu [2 ]
Zhou, Jun [1 ,3 ]
机构
[1] Nankai Univ, Coll Life Sci, State Key Lab Med Chem Biol, Tianjin 300071, Peoples R China
[2] Georgia State Univ, Dept Biol, Atlanta, GA 30303 USA
[3] Shandong Normal Univ, Minist Educ, Key Lab Mol & Nano Probes, Inst Biomed Sci,Coll Life Sci,Key Lab Anim Resist, Jinan 250014, Peoples R China
基金
中国国家自然科学基金;
关键词
HDAC6; Viral infection; Viral pathogenesis; Antiviral therapy; HISTONE DEACETYLASE 6; VIRUS ENTRY; INTERFERON RESPONSE; PLASMA-MEMBRANE; I INTERFERON; ACETYLATION; BETA; ACTIVATION; INDUCTION; HIV;
D O I
10.1016/j.pharmthera.2016.04.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Histone deacetylase 6 (HDAC6), a cytoplasmic enzyme important for many biological processes, has recently emerged as a critical regulator of viral infection. HDAC6 exerts this function either directly, via orchestrating various stages of the viral life cycle, or indirectly via modulating cytokine production by host cells. The broad influence of HDAC6 on viral pathogenesis suggests that this protein may represent an antiviral target. However, the feasibility of targeting HDAC6 and the optimal strategy by which this could be accomplished cannot simply be concluded from individual studies. The primary challenge in developing HDAC6-targeted therapies is to understand how its antiviral effect can be selectively harnessed. As a springboard for future investigations, in this review we recapitulate recent findings on the diverse roles of HDAC6 in viral infection and discuss its alluring potential as a novel antiviral target (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:120 / 125
页数:6
相关论文
共 52 条
  • [1] BET bromodomain inhibition as a novel strategy for reactivation of HIV-1
    Banerjee, Camellia
    Archin, Nancie
    Michaels, Daniel
    Belkina, Anna C.
    Denis, Gerald V.
    Bradner, James
    Sebastiani, Paola
    Margolis, David M.
    Montano, Monty
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 2012, 92 (06) : 1147 - 1154
  • [2] Influenza A virus uses the aggresome processing machinery for host cell entry
    Banerjee, Indranil
    Miyake, Yasuyuki
    Nobs, Samuel Philip
    Schneider, Christoph
    Horvath, Peter
    Kopf, Manfred
    Matthias, Patrick
    Helenius, Ari
    Yamauchi, Yohei
    [J]. SCIENCE, 2014, 346 (6208) : 473 - 477
  • [3] Chattopadhyay S, 2013, MBIO, V4
  • [4] HDAC6 regulates cellular viral RNA sensing by deacetylation of RIG-I
    Choi, Su Jin
    Lee, Hyun-Cheol
    Kim, Jae-Hoon
    Park, Song Yi
    Kim, Tae-Hwan
    Lee, Woon-Kyu
    Jang, Duk-Jae
    Yoon, Ji-Eun
    Choi, Young-Il
    Kim, Seihwan
    Ma, JinYeul
    Kim, Chul-Joong
    Yao, Tso-Pang
    Jung, Jae U.
    Lee, Joo-Yong
    Lee, Jong-Soo
    [J]. EMBO JOURNAL, 2016, 35 (04) : 429 - 442
  • [5] Systems biology of virus entry in mammalian cells
    Damm, Eva-Maria
    Pelkmans, Lucas
    [J]. CELLULAR MICROBIOLOGY, 2006, 8 (08) : 1219 - 1227
  • [6] Coupling viruses to dynein and kinesin-1
    Dodding, Mark P.
    Way, Michael
    [J]. EMBO JOURNAL, 2011, 30 (17) : 3527 - 3539
  • [7] The interferon response circuit: Induction and suppression by pathogenic viruses
    Haller, O
    Kochs, G
    Weber, F
    [J]. VIROLOGY, 2006, 344 (01) : 119 - 130
  • [8] Posttranslational Modifications of Tubulin and the Polarized Transport of Kinesin-1 in Neurons
    Hammond, Jennetta W.
    Huang, Chun-Fang
    Kaech, Stefanie
    Jacobson, Catherine
    Banker, Gary
    Verhey, Kristen J.
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2010, 21 (04) : 572 - 583
  • [9] Convergence of the NF-κB and IRF pathways in the regulation of the innate antiviral response
    Hiscott, John
    [J]. CYTOKINE & GROWTH FACTOR REVIEWS, 2007, 18 (5-6) : 483 - 490
  • [10] HDAC6 is a microtubule-associated deacetylase
    Hubbert, C
    Guardiola, A
    Shao, R
    Kawaguchi, Y
    Ito, A
    Nixon, A
    Yoshida, M
    Wang, XF
    Yao, TP
    [J]. NATURE, 2002, 417 (6887) : 455 - 458