教育经历

2002-2006  华中师范大学生命科学学院， 学士

2006-2012  中国科学院生物物理研究所， 博士

工作经历与任职

2013-2018 University of North Carolina at Chapel Hill, NC, US，Postdoc

2018-2020 University of North Carolina at Chapel Hill, NC, US，Research Associate

2020-至今 武汉大学医学研究院，教授

研究领域及研究成果

心肌梗死等心血管疾病严重威胁人类健康，其导致的死亡率已连续数年高于肿瘤及其他疾病。不可逆性心肌损伤，永久性心肌细胞数量减少以及梗死区域疤痕组织的形成最终导致患者心功能恶化和心力衰竭。心肌细胞重编程技术可将梗死区内源性成纤维细胞转化为有功能的心肌细胞并改善心脏功能，为心血管疾病模型、心脏再生医学等相关领域提供了新的生长点，具有重要的科学意义和转化医学价值。本实验室前期建立了高效的心肌细胞重编程体系（Circulation Research, 2015）,并结合单细胞转录组测序技术描绘了高清晰的纤维细胞到心肌细胞的命运转换图谱，进而揭示了此过程中细胞周期调控、mRNA剪切调控等分子机关调控细胞命运决定的分子机制(Nature，2017)。我们将综合应用传统的分子生物学、细胞生物学和遗传学，结合先进的单细胞组学和生物信息学分析，剖析心肌细胞命运决定的分子机制及重编程与衰老、炎症、代谢的互作关系,协同推进心肌梗死等心血管疾病在体逆转的临床转化应用，为探索治疗心血管疾病提供新的思路和途径。

代表性论文

1. Wang, L., Huang, P., Near, D., Xu, Y., Liu, J. and Qian, L. Isoform Specific Effects of Mef2C during Direct Cardiac Reprogramming. (2020) Cells, 9(2), 268.

2. Liu Z*., Wang L.*, Welch J.*, Ma H., Zhou Y., Vaseghi H.R., Yu S., Wall J.B., Alimohamadi S., Zheng M., Yin C., Shen W., Prins J., Liu J.and Qian L. (2017) Single-cell transcriptomics reconstructs fate conversion from fibroblast to cardiomyocyte. Nature, 551(7678):100-104. * Equal contribution

3. Wang L., Liu J. and Qian L. (2017) In vivo Lineage Reprogramming of Fibroblasts to Cardiomyocytes for Heart Regeneration. In: In Vivo Reprogramming in Regenerative Medicine (Stem Cell Biology and Regenerative Medicine) (Yilmazer ed) Springer International Publishing AG. p45-63.

4. Wang L. *, Liu Z. *, Yin C., Asfour H., Chen O., Li Y., Bursac N., Liu J. and Qian L. (2015) Stoichiometry of Gata4, Mef2c and Tbx5 influences the efficiency and quality of iCM reprogramming. Circ Res. 116, 237-244. * Equal contribution. (Editor’s Pick; highlighted on cover; Previewed in Muraoka et al., Circ Res, 116:216-218.)

5. Wang L., Liu Z., Yin C., Zhou Y., Liu J. and Qian L. (2015) Improved generation of induced cardiomyocytes using a polycistronic construct expressing optimal ratio of Gata4, Mef2c and Tbx5. J Vis Exp. (105), e53426

6. Wang L, Qian L. miR-24 regulates intrinsic apoptosis pathway in mouse cardiomyocytes. (2014) PLoS One. 15; 9(1):e85389.

7. Wang, L.*, Li, Q.*, Wu, L., Liu S., Zhang Y., Yang X., Zhu P., Zhang H., Zhang, K., Lou J., Liu P., Tong L., Sun, F., and Fan, Z. (2012) Identification of SERPINB1 as a physiological inhibitor of human granzyme H. Journal of Immunology, 190, 1319-1330. * Equal contribution. (Highlighted by the same issue: keeping granzyme H in check)

8. Wang, L., Zhang, K., Wu, L., Liu, S., Zhang, H., Zhou, Q., Tong, L., Sun, F., and Fan, Z. (2012) Structural insights into the substrate specificity of human granzyme H: the functional roles of a novel RKR motif. Journal of Immunology,188, 765-773.

获奖情况