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6月06日 清华大学生物论坛
发布时间:2013-05-21关键字:

 

STEPHEN DALTON, Ph.D.

Professor, GRA Eminent Scholar and Chair in Molecular Cell Biology, University of Georgia

 

EDUCATION 

1981-1983       BSc (Biochemistry and Cell Biology): Flinders University of South Australia

1984               BSc Honors, First Class: Flinders University School of Medicine

1985-1988       Ph.D. (Biochemistry and Molecular Biology): University of Adelaide,   

 

PROFESSIONAL EXPERIENCE

1992-1996      Assistant Member, Roche Institute of Molecular Biology     

                      Adjunct  Assistant Professor, Department of Biological Sciences, Columbia

                      University

1996-2003      Senior Lecturer, University of Adelaide, South Australia 

2002-2003      Scientific Director, Luminis-BresaGen Cell Therapy Program, 

2003-present  Professor

                     GRA Eminent Scholar and Chair in Molecular Cell Biology, University of Georgia  

2012-present  Director, Center for Molecular Medicine, University of Georgia

 

Title:  Using pluripotent stem cells to model development and disease

 

Abstract:

The epicardium plays critical roles in cardiac development, homeostasis and potentially in repair following mechanical and ischemic injury. In this talk, I describe the highly efficient differentiation of human pluripotent cells (hPSCs) into Wt1+ epicardium. At the molecular level, hPSC-derived epicardium (EpiCs) are indistinguishable from their in vivo counterparts and like authentic epicardium, are derived from Isl1+ Nkx2.5+ splanchnic mesoderm progenitors that also have cardiomyocyte differentiation capacity. hPSC-derived EpiCs respond to signaling molecules known to impact on epicardium cell fate decisions in vivo as shown by their differentiation into smooth muscle cells or fibroblasts in response to PDGFβ and PDGFα, respectively. When transplanted into chick embryos, EpiCs incorporate into the host epicardium, invade the underlying myocardium and differentiate into myofibroblasts and smooth muscle cells that assemble into coronary vessels. These findings have significant implications for our understanding of human cardiovascular development and for the generation of cell therapies and drug discovery.

 

Venue: Room143, New Biology Building, THU

Time: June 6 (Thu), 2013; 14:00

Host: Prof. Qin Shen

 




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