The research proposed has two complementary goals. The first goal is to? elucidate the biological properties of adult stem cells (ASCs) that renew human tissues. The? second is to translate human ASC discoveries into advances in cellular medicine. For decades,? lack of critical knowledge about ASCs has been a formidable wall at the frontier of ASC? research and cellular medicine. Three intractable research challenges form this wall. Methods? for exact identification of ASCs are lacking, ASCs are difficult to produce in large quantities,? and, therefore, important biological features of ASCs remain obscure. To address these? challenges, during the past 14 years as a principal investigator, the applicant undertook? research with genetically-engineered mouse cells that modeled essential unique properties of? ASCs. These properties are asymmetric self-renewal and immortal DNA strand co-segregation,? two defining features of ASCs. A series of reports from the applicant?s laboratory established? the relevance of discoveries made with the mouse ASC models to rodent ASCs in vivo. These? discoveries established an innovative foundation for identifying ASCs, expanding ASCs in? culture, and investigating ASC cellular and molecular properties. With NDPA support, the? applicant will change the direction of his research program, forged with rodent ASC studies, to? focus on human ASCs and their conversion into embryonic stem cell (ESC)-like cells. Human? ASCs responsible for liver, hematopoietic cells, pancreas, and hair will be the focus of research? with the goal of developing both pre-clinical and clinical applications for cellular medicine. The? applicant?s research program enjoys collaborations with several laboratories from diverse? scientific disciplines and technological fields, including mathematics, chromosome biology,? mass spectrometry, bioinformatics, genomics, electrical engineering, computer sciences, and? the cell products industry. These interactions will complement research to expand selected? human ASCs, develop tools for their exact identification, and advance ASCs as effective cellular? medicines for human disease.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
NIH Director’s Pioneer Award (NDPA) (DP1)
Project #
7DP1OD000805-02
Application #
7292778
Study Section
Special Emphasis Panel (ZGM1-NDPA-G (P2))
Program Officer
Jones, Warren
Project Start
2006-09-28
Project End
2011-07-31
Budget Start
2007-09-04
Budget End
2008-07-31
Support Year
2
Fiscal Year
2007
Total Cost
$995,000
Indirect Cost
Name
Boston Biomedical Research Institute
Department
Type
DUNS #
058893371
City
Watertown
State
MA
Country
United States
Zip Code
02472
Huh, Y H; Sherley, J L (2014) Decreased H3K27 and H3K4 trimethylation on mortal chromosomes in distributed stem cells. Cell Death Dis 5:e1554
Paré, Jf; Sherley, Jl (2013) Ex vivo Expansion of Human Adult Pancreatic Cells with Properties of Distributed Stem Cells by Suppression of Asymmetric Cell Kinetics. J Stem Cell Res Ther 3:149
Huh, Yang Hoon; Cohen, Justin; Sherley, James L (2013) Higher 5-hydroxymethylcytosine identifies immortal DNA strand chromosomes in asymmetrically self-renewing distributed stem cells. Proc Natl Acad Sci U S A 110:16862-7
Huh, Yang Hoon; Sherley, James L (2011) Molecular cloaking of H2A.Z on mortal DNA chromosomes during nonrandom segregation. Stem Cells 29:1620-7
Noh, Minsoo; Smith, Janet L; Huh, Yang Hoon et al. (2011) A resource for discovering specific and universal biomarkers for distributed stem cells. PLoS One 6:e22077
Pare, Jean-Francois; Sherley, James L (2011) Culture environment-induced pluripotency of SACK-expanded tissue stem cells. J Biomed Biotechnol 2011:312457
Taghizadeh, Rouzbeh; Noh, Minsoo; Huh, Yang Hoon et al. (2010) CXCR6, a newly defined biomarker of tissue-specific stem cell asymmetric self-renewal, identifies more aggressive human melanoma cancer stem cells. PLoS One 5:e15183