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个人简介

梁平,浙江大学转化医学研究院及浙江大学医学院附属第一医院双聘教授、博士生导师。 教育背景 1、2005.09-2010.06,北京大学,神经科学,博士(导师:王克威教授) 2、2008.01-2009.01,加州大学戴维斯分校,生理与膜生物学,访问学者(导师:郑劼教授) 3、2000.09-2005.06,中国医科大学,临床医学,学士 工作经历 1、2014.04-至今,浙江大学转化医学研究院,教授 2、2011.05-2014.04,斯坦福大学,心血管研究所,博士后(导师:Joseph Wu教授) 3、2010.09-2011.04,百泰生物药业有限公司,医学研发部,项目经理

研究领域

我实验室目前的研究集中于人胚胎干细胞(hESC)以及由体细胞(收集于皮肤、血液和尿液样本)经过特异性转录因子介导的重编程而获得的人诱导多能干细胞(hiPSC)。应用多能干细胞(hESC和hiPSC)作为主要研究模型,我们专注于不同类型的心血管疾病研究,特别是各种心肌病、离子通道病、心律失常以及高血压。利用建立的病人特异的iPS细胞系,我们旨在高效率、高质量地将其定向分化生成病人特异的hiPSC来源的心肌细胞和内皮细胞。结合多种技术如干细胞生物学、定向分化、电生理、钙成像、二代高通量测序、药理学和生物化学等,我们试图从基础研究和转化医学研究两个方面来探讨感兴趣的心血管疾病,其中包括:i)基于hiPSC技术的细胞疾病建立,ii)疾病表型研究以及疾病分子机制的深入探索,iii)基于hiPSC技术的高通量、个体化的药物研发和筛选(包括药物疗效和药物心脏毒性检测)。此外,我们还将基因组编辑技术应用于已有的hES或者hiPS细胞系,包括两方面应用:i)在正常hES或者hiPS细胞系基础上进行基因组编辑以获得“加强版”细胞疾病模型;ii)在已建立的病人特异的hiPS细胞系基础上进行基因校正以纠正该疾病表型。

近期论文

查看导师最新文章 (温馨提示:请注意重名现象,建议点开原文通过作者单位确认)

1、Ebert AD, Kodo K, Liang P, Wu H, Huber BC, Riegler J, Churko J, Lee J, Almeida PE, Lan F, Diecke S, Burridge PW, Gold JD, Mochly-Rosen D, Wu JC. Characterization of the molecular mechanisms underlying increased ischemic damage in the aldehyde dehydrogenase 2 genetic polymorphism using a human induced pluripotent stem cell model system. Science Translational Medicine 2014; 6 (255): 255ra130 2、Sharma A, Marceau CD, Hamaguchi R, Burridge P, Rajarajan K, Churko J, Wu H, Sallam K, Matsa E, Sturzu A, Che Y, Ebert A, Diecke S, Liang P, Red-Horse K, Carette JE, Wu SM, Wu JC. Human induced pluripotent stem cell-derived cardiomyocytes as an in vitro model for coxsackievirus B3-induced myocarditis and antiviral drug screening platform. Circulation Research 2014; 115 (6): 556-66 3、Wang Y*, Liang P*, Lan F*, Wu H*, Lisowski L, Gu M, Hu S, Kay M, Urnov F, Shinnawi R, Gold J, Gepstein L, Wu JC. Genome editing of isogenic human induced pluripotent stem cells recapitulates Long QT phenotype for drug testing. JACC 2014; 64 (5): 451-9(*并列第一作者) 4、Sanchez VF, Lee AS, Hu S, Abilez OJ, Liang P, Lan F, Huber B, Ong S, Hong W, Huang M, Wu JC. Effect of human donor cell source on differentiation and function of cardiac induced pluripotent stem cells. JACC 2014; 64 (5): 436-48 5、Liang P, Du J. Human induced pluripotent stem cell for modeling cardiovascular diseases. Regenerative Medicine Research 2014; 2:4 6、Navarrete EG*, Liang P*, Lan F*, Sanchez-Freire V, Simmons CS, Gong T, Sharma A, Burridge PW, Patlolla B, Lee AS, Beygui RE, Bers DM, Wu JC. Screening drug- induced arrhythmia events using human induced pluripotent stem cell-derived cardiomyocytes and low-impedance microelectrode arrays. Circulation 2013; 128: S3-S13(*并列第一作者) 7、Tang Y, Liang P, Zhou J, Lu Y, Lei L, Bian X, and Wang K. Auxiliary KChIP4a suppresses A-type K+ current through ER retention and promoting closed-state inactivation of Kv4 channels. JBC 2013; 288 (21): 14727-41 8、Liang P*, Lan F*, Lee AS*, Gong T, Sanchez VF, Wang Y, Diecke S, Sallam K, Knowles JW, Wang PJ, Nguyen PK, Bers DM, Robbins RC, Wu JC. Drug screening using a library of human induced pluripotent stem cell derived cardiomyocytes reveals disease specific patterns of cardiotoxicity. Circulation 2013; 127 (16): 1677-1691(由Dan Roden和Charles Hong配发评论)(2013 年度基础研究领域最佳论文)(*并列第一作者) 9、Lan F*, Lee AS*, Liang P*, Sanchez VF, Nguyen PK, Wang L, Han L, Yen M, Wang Y, Sun N, Abilez OJ, Hu S, Ebert AD, Navarrete EG, Simmons CS, Wheeler M, Pruitt B, Lewis R, Yamaguchi Y, Ashley EA, Bers DM, Robbins RC, Longaker MT, Wu JC. Abnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cells. Cell Stem Cell 2013; 12 (1): 101-13(Faculty 1000推荐“必读”文章)(*并列第一作者) 10、Wang Y, Zhang W, Hu S, Lan F, Lee AS, Huber B, Lisowski L, Liang P, Huang M, Almeida PE, Won J, Sun N, Robbins RC, Kay MA, Urnov FD, Wu JC. Genome editing of human embryonic stem cells and induced pluripotent stem cells with zinc finger nucleases for cellular imaging. Circulation Research 2012; 111 (12): 1494-503(封面文章)(由G Courties和M Nahrendorf配发评论) 11、Ebert AD, Liang P, Wu JC. Induced pluripotent stem cells as a disease modeling and drug screening platform. Journal of Cardiovascular Pharmacology 2012; 60 (4): 408-16 12、Liang P, Chen H, Cui Y, Wang K. Functional rescue of Kv4.3 channel tetramerization mutants by KChIP4a. Biophysical Journal 2010; 98 (12): 2867-76 13、Zhang Y*, Su P*, Liang P, Liu T, Liu X, Liu X, Zhang B, Han T, Zhu Y, Yin D, Li J, Zhou Z, Wang K, Wang Y. The DREAM protein negatively regulates the NMDA receptor through interaction with the NR1 subunit. Journal of Neuroscience 2010; 30 (22): 7575-86(*并列第一作者) 14、Liang P*, Wang H*, Chen H*, Cui Y, Gu L, Chai J, Wang K. Structural insights into KChIP4a modulation of Kv4.3 inactivation. JBC 2009; 284 (8): 4960-4967(*并列第一作者) 15、Cui Y, Liang P, Wang K. Enhanced trafficking of tetrameric Kv4.3 channels by KChIP1 clamping. Neurochemical Research 2008; 33 (10): 2078-84

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