研究生导师


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  研究生导师
邓国平 副研究员
发布日期:2018-09-28 浏览次数: 字号:[ ]

 联系方式

北京大学基础医学院免疫学系

北京市海淀区学院路38号, 邮编:100191

电话:86-10-82801694

邮箱:gdeng@pku.edu.cn

 

教育经历

2003-2009,理学博士,北京大学生命科学学院

1998-2002,理学学士,兰州大学生命科学学院

 

工作经历

2018-至今,副研究员,北京大学基础医学院免疫系

2017-2018,研究助理,美国宾夕法尼亚大学佩尔曼医学院

2011-2017,博士后,美国宾夕法尼亚大学佩尔曼医学院/费城儿童医院

 

科学协会会员

The American Association of Immunologists, Chinese Society for Cell Biology, Asia-Pacific Association of Medicine and Bio-Immunology, Guest editor of theJournal of Leukocyte Biology 

科研领域描述

 

Dr. Deng received his Ph.D. degree from Peking University in 2009 (mentor: Dr. Jindong Zhao). His postdoctoral trainings were finished in the labs of Dr. Mark Greene, ConstantinosKoumenis and Paula Oliver in Perelman School of Medicine, University of Pennsylvania and Children’s Hospital of Philadelphia from 2011 to 2017. After this, he worked as Research Associate in the lab of Dr. James Riley in Perelman School of Medicine, University of Pennsylvania in 2018. He is currently a tenure-track assistant professor at the Department of Immunology, Health Science Center, Peking University.

 

T cells play critical roles in the adaptive immune system. The overall research interest of Deng lab is to investigate the mechanism of T cell activation, tolerance and engineering for effective immunotherapy. We use genetic and immunological approaches to determine the signaling pathways regulating T cell function in models of autoimmunity and tumor immunity. In addition, we collaborate extensively with clinics in analyzing the T cell function of patients. We are interested in studies aimed at translating fundamental understanding of T cell function into new therapies for autoimmune diseases and cancer.

 

代表性文章(# 第一作者, *通讯作者)

1. Ma T, Song X, Piccirillo CA, Deng G*and Greene MI. A structure-guided delineation of FOXP3 regulation mechanism in IPEX. Chapter of Springer Nature Book: T Regulatory Cells in Human Health and Diseases.2021; https://doi.org/10.1007/978-981-15-6407-9_2.

2. Deng G*, Song X, Fujimoto S, Piccirillo CA, Nagai Y and Greene MI*. Foxp3 Post-translational Modifications and Treg Suppressive Activity. Front. Immunol. 2019; https://doi.org/10.3389/fimmu.2019.02486.

3. Deng G*, Song X and Greene MI*. FoxP3 in Treg cell biology: a molecular and structural perspective. Clin Exp Immunol. 2019; https://doi.org/10.1111/cei.13357.

4. Deng G. Tumor-infiltrating regulatory T cells: origins and features. Am J Clin Exp Immunol 2018; 7: 81-87.

5. Layman AAK#, Deng G#, O'Leary CE#, Tadros S, Thomas RM, Dybas JM, Moser EK, Wells AD, Doliba NM and Oliver PM. Ndfip1 restricts mTORC1 signalling and glycolysis in regulatory T cells to prevent autoinflammatory disease. Nat Commun 2017; 8: 15677.

6. O'Leary CE, Riling CR, Spruce LA, Ding H, Kumar S, Deng G, Liu Y, Seeholzer SH and Oliver PM. Ndfip-mediated degradation of Jak1 tunes cytokine signalling to limit expansion of CD4+ effector T cells. Nat Commun 2016; 7: 11226.

7. Deng G, Nagai Y, Xiao Y, Li Z, Dai S, Ohtani T, Banham A, Li B, Wu SL, Hancock W, Samanta A, Zhang H and Greene MI. Pim-2 Kinase Influences Regulatory T Cell Function and Stability by Mediating Foxp3 Protein N-terminal Phosphorylation. J Biol Chem 2015; 290: 20211-20220.

8. Li Z, Lin F, Zhuo C, Deng G, Chen Z, Yin S, Gao Z, Piccioni M, Tsun A, Cai S, Zheng SG, Zhang Y and Li B. PIM1 kinase phosphorylates the human transcription factor FOXP3 at serine 422 to negatively regulate its activity under inflammation. J Biol Chem 2014; 289: 26872-26881.

9. Xiao Y, Nagai Y, Deng G, Ohtani T, Zhu Z, Zhou Z, Zhang H, Ji MQ, Lough JW, Samanta A, Hancock WW and Greene MI. Dynamic interactions between TIP60 and p300 regulate FOXP3 function through a structural switch defined by a single lysine on TIP60. Cell Rep 2014; 7: 1471-1480.

10. Deng G, Xiao Y, Zhou Z, Nagai Y, Zhang H, Li B and Greene MI. Molecular and biological role of the FOXP3 N-terminal domain in immune regulation by T regulatory/suppressor cells. Exp Mol Pathol 2012; 93: 334-338.

 

 




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