Human Embryonic Stem Cells (hESC) have remarkable potential for studies of fundamental human developmental biology. The principal goal of this project is to establish the Burnham Stem Cell Center to facilitate collaborative research in the basic biology of hESC and encourage new researchers to enter the field. The Center will enable new and established investigators to develop the utility of hESC as a model system for a diverse range of biological and medical problems. The proposal for the Center has two specific aims.
For Aim 1, we will establish a shared core laboratory that provides state-of-art equipment and expert support for area investigators and training in hESC methods. Core programs will be tightly focused on specific goals to provide technical support and expertise, develop new technologies, and train new investigators. The Core Programs are (1) Cell Culture and Maintenance, (2) Cell Characterization, (3) High Throughput Analysis Technology Development, and (4) Data Sharing and Training. These programs will use NIH Registry Cell lines WA01, WA09, and WA14. To encourage new investigators and collaborations, the Center will share responsibility for an annual ten-day NIH-sponsored T15 training course in hESC technology, provide 2-3 day training courses for visiting scientists, sponsor a website for sharing information about hESC, host scientific and ethics symposia twice a year, and support the monthly meetings of the Southern California Stem Cell Consortium.
Aim 2 is to sponsor competitive pilot projects that take advantage of the unique potential of hESC. We will support four early-phase, hypothesis-driven pilot projects that address fundamental questions of hESC biology. These pilot projects include investigations of chemical inducers of differentiation, epigenetic controls of differentiation, development of novel high-resolution real time imaging technology to study hESCs in vitro, and molecular and developmental controls of hESC self-renewal. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
1P20GM075059-01
Application #
6964568
Study Section
Special Emphasis Panel (ZGM1-GDB-8 (SC))
Program Officer
Zatz, Marion M
Project Start
2005-08-01
Project End
2008-07-31
Budget Start
2005-08-01
Budget End
2006-07-31
Support Year
1
Fiscal Year
2005
Total Cost
$1,060,699
Indirect Cost
Name
Sanford-Burnham Medical Research Institute
Department
Type
DUNS #
020520466
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Singec, Ilyas; Crain, Andrew M; Hou, Junjie et al. (2016) Quantitative Analysis of Human Pluripotency and Neural Specification by In-Depth (Phospho)Proteomic Profiling. Stem Cell Reports 7:527-542
Acevedo, Lisette M; Lindquist, Jeffrey N; Walsh, Breda M et al. (2015) hESC Differentiation toward an Autonomic Neuronal Cell Fate Depends on Distinct Cues from the Co-Patterning Vasculature. Stem Cell Reports 4:1075-88
Tobe, Brian T D; Snyder, Evan Y; Nye, Jeffrey S (2011) Modeling complex neuropsychiatric disorders with human induced pluripotent stem cells. Curr Opin Pharmacol 11:521-7
Carro, Maria Stella; Lim, Wei Keat; Alvarez, Mariano Javier et al. (2010) The transcriptional network for mesenchymal transformation of brain tumours. Nature 463:318-25
Ourednik, Vaclav; Ourednik, Jitka; Xu, Yifang et al. (2009) Cross-talk between stem cells and the dysfunctional brain is facilitated by manipulating the niche: evidence from an adhesion molecule. Stem Cells 27:2846-56
Brill, Laurence M; Xiong, Wen; Lee, Ki-Bum et al. (2009) Phosphoproteomic analysis of human embryonic stem cells. Cell Stem Cell 5:204-13
Jeyakumar, Mylvaganam; Lee, Jean-Pyo; Sibson, Nicola R et al. (2009) Neural stem cell transplantation benefits a monogenic neurometabolic disorder during the symptomatic phase of disease. Stem Cells 27:2362-70
Wakeman, Dustin R; Hofmann, Martin R; Redmond Jr, D Eugene et al. (2009) Long-term multilayer adherent network (MAN) expansion, maintenance, and characterization, chemical and genetic manipulation, and transplantation of human fetal forebrain neural stem cells. Curr Protoc Stem Cell Biol Chapter 2:Unit2D.3
Wu, Dongmei; Pang, Yuhong; Ke, Yuehai et al. (2009) A conserved mechanism for control of human and mouse embryonic stem cell pluripotency and differentiation by shp2 tyrosine phosphatase. PLoS One 4:e4914
Lee, Jean-Pyo; Tsai, David J; In Park, Kook et al. (2009) The dynamics of long-term transgene expression in engrafted neural stem cells. J Comp Neurol 515:83-92

Showing the most recent 10 out of 14 publications