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首頁 全所PI名錄
  • 侯法建
  • 研究員,研究組長,博士生導師
  • E-mail: fhou@@sibcb.ac.cn
  • 實驗室主頁: 
    個人簡介:
  •   1995年畢業(yè)于武漢大學,獲學士學位;2001年畢業(yè)于中科院上海生化所,獲博士學位。2001年11月至2012年1月于美國德州大學西南醫(yī)學中心從事博士后研究。2012年2月起,在中科院上海生物化學與細胞生物學研究所任研究員,研究組長。

    社會任職:
  •  
    研究方向:
  • 天然免疫與炎癥的生化細胞機理及相關疾病
    研究工作:
  •   當病原體入侵高等有機體時,會引發(fā)免疫反應,包括天然免疫和適應性免疫。天然免疫反應起始于宿主細胞的受體分子對病原體上的特異分子或者其它“異己”成分的識別,隨后激活特定的信號通路,誘導相應基因表達,防御病原體侵染。譬如當病毒感染細胞時,病毒相關的核酸分子會被細胞內的受體分子識別而激活相應的信號通路,誘導抗病毒的干擾素產生。天然免疫反應能夠為有機體提供及時的保護,但是其信號異常也可能導致自身免疫疾病等后果。腫瘤發(fā)生過程中產生的危險信號分子也可以激活天然免疫反應,誘導炎癥。我們近期聚焦RIG-I-MAVS信號通路,利用生物化學和分子生物學方法在細胞和動物水平上來解析其中的分子細胞機制,研究該信號通路與自身免疫疾病發(fā)生的相關性及其在腫瘤治療中的功能作用。

    承擔科研項目情況:
    代表論著:
    1. Li J#, Zhang R, Wang C, Li J, Zhu< J, Ren M, Jiang Y, Hou X, Du Y, Wu Q, Qi S, Li L, Chen S, Yang H, Hou F* (2023) WDR77 inhibits prion-like aggregation of MAVS to limit antiviral innate immune response. Nature Communications, doi.org/10.1038/s41467-023-40567-5
    2. Zhang R#, Hou X#, Wang C, Li J, Zhu J, Jiang Y, Hou F* (2022) The endoplasmic reticulum ATP13A1 is essential for MAVS-mediated antiviral innate immunity. Advanced Science, doi: 10.1002/advs.202203831
    3. Qi S#, Wang C#, Zhang R#, Zhu J, Hou X, Jiang Y, Li J, Ren M, Li M, Hou F* (2022) Human STING is regulated by an autoinhibitory mechanism for Type I interferon production. J Innate Immun, doi: 10.1159/000521734
    4. Yang H#,*, Lyu Y#, Hou F* (2020) SARS-CoV-2 infection and the antiviral innate immune response. J Mol Cell Biol, doi:10.1093/jmcb/mjaa071
    5. Zhu W#, Li J#, Zhang R, Cai Y, Wang C, Qi S, Chen S, Liang X, Qi N*, Hou F* (2019) TRAF3IP3 mediates the recruitment of TRAF3 to MAVS for antiviral innate immunity. EMBO J, doi: 10.15252/embj.2019102075
    6. Cadena C, Ahmad S, Xavier A, Willemsen J, Park S, Park J, Oh S, Fujita T, Hou F, Binder M, Hur S* (2019) Ubiquitin-Dependent and -Independent Roles of E3 Ligase RIPLET in Innate Immunity. Cell, 177, 1-14
    7. Zhou P, Ding X, Wan X, Liu L, Yuan X, Zhang W, Hui X, Meng G, Xiao H, Li B, Zhong J, Hou F, Deng L, Zhang Y* (2018) MLL5 suppresses antiviral innate immune response by facilitating STUB1-mediated RIG-I degradation. Nat Commun, |9:1243|DOI: 10.1038/s41467-018-03563-8
    8. Li X, Gadzinsky A, Gong L, Tong H, Calderon V, Li Y, Kitamura D, Klein U, Langdon WY, Hou F, Zou YR, Gu H* (2018) Cbl Ubiquitin Ligases Control B Cell Exit from the Germinal-Center Reaction. Immunity, 48, 530-541
    9. Qi N#, Shi Y#, Zhang R, Zhu W, Yuan B, Li X, Wang C, Zhang X, Hou F* (2017) Multiple truncated isoforms of MAVS prevent its spontaneous aggregation in antiviral innate immune signalling. Nat Commun, |8:15676|DOI: 10.1038/ncomms15676
    10. Shi Y#, Yuan B#, Zhu W#, Zhang R, Li L, Hao X, Chen S, Hou F* (2017) Ube2D3 and Ube2N are essential for RIG-I-mediated MAVS aggregation in antiviral innate immunity. Nat Commun, |8:15138| DOI:10.1038/ncomms 15138
    11. Shi Y#, Yuan B#, Qi N#, Zhu W, Su J, Li X, Qi P, Zhang D, Hou F* (2015) An autoinhibitory mechanism modulates MAVS activity in antiviral innate immune response. Nat Commun, |6:78111|DOI: 10.1038/ncomms8811
    12. Xu H, He X, Zheng H, Huang L, Hou F, Yu Z, Cruz MJ, Borkowski B, Zhang X*, Chen ZJ*, Jiang Q-X* (2014) Structural basis for the prion-like MAVS filaments in antiviral innate immunity. ELife, 3, e01489
    13. Hou F, Sun L, Zheng H, Skaug B, Jiang QX, and Chen ZJ* (2011) MAVS Forms Functional Prion-like Aggregates to Activate and Propagate Antiviral Innate Immune Response. Cell, 146, 448-461
    14. Chu CW, Hou F, Zhang J, Phu L, Loktev AV, Kirkpatrick DS. Jackson PK, Zhao Y, and Zou H* (2011) A novel acetylation of beta-tubulin by San modulates microtubule polymerization via down-regulating tubulin incorporation. Mol Biol Cell, 22, 448-456
    15. Zeng W, Sun L, Jiang X, Chen X, Hou F, Adhikari A, Xu M, and Chen ZJ* (2010) Reconstitution of the RIG-I pathway reveals a signaling role of unanchored polyubiquitin chains in innate immunity. Cell, 141, 315-330
    16. Gordillo M, Vega H, Trainer AH, Hou F, Sakai N, Luque R, Kayserili H, Basaran S, Skovby F, Hennekam RC, Uzielli ML, Schnur RE, Manouvrier S, Chang S, Blair E, Hurst JA, Forzano F, Meins M, Simola KO, Raas-Rothschild A, Schultz RA, McDaniel LD, Ozono K, Inui K, Zou H and Jabs EW* (2008) The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity. Hum Mol Genet, 17(14), 2172-80
    17. Hou F, Chu CW, Kong X, Yokomori K, and Zou H* (2007) The acetyltransferase activity of San stabilizes the mitotic cohesin at the centromeres in a shugoshin-independent manner. J Cell Biol, 177, 587-597
    18. Hou F, and Zou H* (2005) Two human orthologues of Eco1/Ctf7 acetyltransferases are both required for proper sister-chromatid cohesion. Mol Biol Cell, 16, 3908-3918
    19. Jia J, Zhang L, Zhang Q, Tong C, Wang B, Hou F, Amanai K, and Jiang J* (2005) Phosphorylation by double-time/CKIepsilon and CKIalpha targets cubitus interruptus for Slimb/beta-TRCP-mediated proteolytic processing. Dev Cell, 9, 819-830
    獲獎及榮譽:
    研究組成員:
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