Stem cells are a potentially important source of cells to replace tissues or organs deficient as a result of trauma, disease, or developmental anomalies. This proposal is focused on increasing our understanding of stem cells derived from adult bone marrow. The proposed experiments will examine the molecular mechanisms controlling nuclear reprogramming and plasticity of gene expression exhibited by adult bone marrow-derived cells.
In Specific Aim (1) I plan to develop an in vitro system to model plasticity and nuclear reprogramming as they occur in vivo.
Specific Aim (2) will involve an in depth investigation of the intracellular events that control or modulate the changes in gene expression resulting in different cellular phenotypes.
Specific Aim (3) will use information gained from the above studies to identify the characteristics of hematopoietic stem cells and their derivatives that are responsible for their predilection to contribute to other tissues. The proposed experiments will not only enhance our basic knowledge of stem cell function, but may also result in new clinical approaches for treatment of conditions involving a deficit of tissue repair or regeneration.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32AR051678-02
Application #
6947205
Study Section
Special Emphasis Panel (ZRG1-F05 (20))
Program Officer
Nuckolls, Glen H
Project Start
2004-09-01
Project End
2006-08-31
Budget Start
2005-09-01
Budget End
2006-08-31
Support Year
2
Fiscal Year
2005
Total Cost
$53,492
Indirect Cost
Name
Stanford University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Blau, Helen M; Pomerantz, Jason H (2011) Re""evolutionary"" regenerative medicine. JAMA 305:87-8
Pajcini, Kostandin V; Corbel, Stephane Y; Sage, Julien et al. (2010) Transient inactivation of Rb and ARF yields regenerative cells from postmitotic mammalian muscle. Cell Stem Cell 7:198-213
Palermo, Adam T; Labarge, Mark A; Doyonnas, Regis et al. (2005) Bone marrow contribution to skeletal muscle: a physiological response to stress. Dev Biol 279:336-44