担任 | 复旦大学上海医学院免疫学系PI研究员,博士生导师,系副主任 |
学习与科研 | 1993年 上海医科大学临床医学系 学士 |
研究重点 | 1、重要病原危险信号分子内毒素及其降解对免疫应答及组织炎症的调控作用:感染性肺炎、急性肺损伤、哮喘、肠炎、代谢性疾病、肿瘤。 2、感染与免疫细胞代谢:TLR刺激物对巨噬细胞代谢的重编程及其对固有免疫应答的调控作用。 |
教学专著 | 《医学免疫学》第六版 参编 |
申请的研究项目 | 1. 国家自然科学基金面上项目32170929 2022-2025 负责人 |
承担的教学任务 | 授课 《医学免疫学》本科生学位基础课 《医学免疫学》 MBBS留学生班 《现代免疫学》博士研究生学位专业课 《细胞与分子免疫学进展》研究生专业课 复旦大学基础医学院优秀奖励计划,2018 |
获得的奖励 | |
复旦大学教学成果奖一等奖,2017 | |
代表性论文 | 1. Zou, B., M. Goodwin, D. Saleem, W. Jiang, J. Tang, Y. Chu, R.S. Munford, and M. Lu*. 2021. A highly conserved host lipase deacylates oxidized phospholipids and ameliorates acute lung injury in mice. eLife 10: e70938. (*通讯作者) 2. Feng, J., W. Jiang, X. Cheng, B. Zou, A. Varley, T. Liu, G. Qian, W. Zeng, J. Tang, Q. Zhao, Y. Chu, Y. Wei, X. Li, R. Munford, and M. Lu*. 2021. A host lipase prevents lipopolysaccharide-induced foam cell formation. iScience 24, 103004. (*通讯作者) 3. Jiang, W., J. Le, P.Y. Wang, X. Cheng, M. Smelkinson, W. Dong, C. Yang, Y. Chu, P.M. Hwang, R.S. Munford, and M. Lu*. 2021. Extracellular Acidity Reprograms Macrophage Metabolism and Innate Responsiveness. Journal of immunology 206:3021-3031. (*通讯作者) 4. Munford, R.S.*, J.P. Weiss, and M. Lu*. 2020. Biochemical Transformation of Bacterial Lipopolysaccharide by acyloxyacyl hydrolase reduces host injury and promotes recovery. The Journal of biological chemistry 295:17842-17851. (综述,*共同通讯作者) 5. Qian, G., W. Jiang, B. Zou, J. Feng, X. Cheng, J. Gu, T. Chu, C. Niu, R. He, Y. Chu, and M. Lu*. 2018. LPS inactivation by a host lipase allows lung epithelial cell sensitization for allergic asthma. The Journal of experimental medicine 215:2397-2412. (*通讯作者) 6. Zou, B., W. Jiang, H. Han, J. Li, W. Mao, Z. Tang, Q. Yang, G. Qian, J. Qian, W. Zeng, J. Gu, T. Chu, N. Zhu, W. Zhang, D. Yan, R. He, Y. Chu, and M. Lu*. 2017. Acyloxyacyl hydrolase promotes the resolution of lipopolysaccharide-induced acute lung injury. PLoS pathogens 13:e1006436. (*通讯作者) 7. Lu, M., T. Kho, and R.S. Munford. 2014. Prolonged triglyceride storage in macrophages: pHo trumps pO2 and TLR4. Journal of immunology 193:1392-1397. 8. Lu, M.*, A.W. Varley, and R.S. Munford. 2013. Persistently active microbial molecules prolong innate immune tolerance in vivo. PLoS pathogens 9:e1003339. (*通讯作者,Faculty 1000) 9. Lu, M.*, and R.S. Munford. 2011. The transport and inactivation kinetics of bacterial lipopolysaccharide influence its immunological potency in vivo. Journal of immunology 187:3314-3320. (*通讯作者) 10. Lu, M.*, A.W. Varley, S. Ohta, J. Hardwick, and R.S. Munford. 2008. Host inactivation of bacterial lipopolysaccharide prevents prolonged tolerance following gram-negative bacterial infection. Cell host & microbe 4:293-302. (*共同通讯作者,封面文章) 11. Lu, M., M. Zhang, A. Takashima, J. Weiss, M.A. Apicella, X.H. Li, D. Yuan, and R.S. Munford. 2005. Lipopolysaccharide deacylation by an endogenous lipase controls innate antibody responses to Gram-negative bacteria. Nature immunology 6:989-994. 12. Lu, M., M. Zhang, R.L. Kitchens, S. Fosmire, A. Takashima, and R.S. Munford. 2003. Stimulus-dependent deacylation of bacterial lipopolysaccharide by dendritic cells. The Journal of experimental medicine 197:1745-1754. |
联系方式 | Tel: 86-21-54237751 E-mail: mingfanglu@fudan.edu.cn |