This Program Project addresses among the most important questions in stem cell medicine and biology through responsible studies on the potentials of pluripotent stem cells from humans (hESC) and nonhuman primates (nhpESC) during development in vitro and in utero, and after transplantation in vivo. Conceptually, the overarching themes are the molecular foundations of ESC and Embryonic Germ [EG] cell properties of Pluripotency, Genomic Imprinting, and Differentiation, under the directions of Gerald Schatten, PhD (PD; Project I PI), Roger Pedersen, PhD (co-PD;Project II PI) and Peter Donovan, PhD (co-PD;Project III PI). Each of the three Research Projects, along with three Technological Cores and an administrative one, address interrelated fundamental and pre-clinical problems. Proj I: """"""""Imaging nhpES cells in vitro, in chimerae, and after transplantation."""""""" (G Schatten, PI) investigates the developmental potentials of nhpESC and nhpES derived after nuclear transfer (NTnhpES) by examining chimerae and genomic imprinting. Proj II: """"""""Differentiation and Epigenesis of Pluripotent Stem Cells"""""""" (R. Pedersen, PI) examines the earliest postimplantation embryos, pluripotent cells and their progeny for imprint normalcy, and to determine differentiation stability. Proj III: """"""""Derivation and Safety Testing of Non-Human Primate Embryonic Germ Cell Lines"""""""" (P. Donovan, PI) investigates primordial germ cells in vivo, derives nhpEG and compares their developmental potentials with ESCs, while ANALYZING genomic imprinting in utero and in vitro during reproduction. Imaging Core A (E. Ahrens, Core Director) non-invasively images in utero development, ESC/EGs in vitro, and tracks transplanted nhp/hESC with specific probes in vivo. Primate Core B (L. Hewitson, CD) provides NHP embryos, maintains pregnancies, evaluates, and performs transplants. ADMIN Core C fosters communication, dissemination, and coordination within this P01 and throughout NIH's stem cell research communities by research planning, real-time data transfer, conferences, and scientific exchanges, as well as our advanced lab course 'Frontiers in Human Embryonic Stem Cell Research.'Stem Cell Core D maintains, preserves, and quality controls new and existing nhpES/EG cell lines, distributing them to the projects and freely to other academic investigators. Complementing NIH's new Stem Cell Centers, our multidisciplinary team will make major contributions towards swiftly and accurately addressing key questions whose answers are the essential foundation for stem cell clinical studies.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
3P01HD047675-05S1
Application #
8055259
Study Section
Special Emphasis Panel (ZHD1-DRG-D (GS))
Program Officer
Moss, Stuart B
Project Start
2010-05-01
Project End
2010-09-30
Budget Start
2010-05-01
Budget End
2010-09-30
Support Year
5
Fiscal Year
2010
Total Cost
$11,139
Indirect Cost
Name
Magee-Women's Research Institute and Foundation
Department
Type
DUNS #
119132785
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
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Easley 4th, Charles A; Simerly, Calvin R; Schatten, Gerald (2013) Stem cell therapeutic possibilities: future therapeutic options for male-factor and female-factor infertility? Reprod Biomed Online 27:75-80
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Easley 4th, Charles A; Phillips, Bart T; McGuire, Megan M et al. (2012) Direct differentiation of human pluripotent stem cells into haploid spermatogenic cells. Cell Rep 2:440-6
Lee, Hyo-Sang; Ma, Hong; Juanes, Rita Cervera et al. (2012) Rapid mitochondrial DNA segregation in primate preimplantation embryos precedes somatic and germline bottleneck. Cell Rep 1:506-15
Stringari, Chiara; Sierra, Robert; Donovan, Peter J et al. (2012) Label-free separation of human embryonic stem cells and their differentiating progenies by phasor fluorescence lifetime microscopy. J Biomed Opt 17:046012

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