Recent studies have suggested that a minority of specialized cells in a number of adult tissues including brain and bone marrow are capable of assuming phenotype and function of cells from developmentally unrelated tissues. This observation has been termed plasticity and has potentially far-reaching implications for therapeutic applications. Controversy surrounds the question of whether the remarkable hematopoietic activity recovered from preparations of muscle tissue represents a similar example of developmental plasticity or merely indicates trafficking of marrow cells to muscle. To date this has only been examined in chimeric murine models generated using lethal irradiation. Resolution of this question is directly relevant to any potential application and modification of such cells. Therefore, the major objective of this proposal is to develop a sufficiently rigorous assay to determine the developmental origin of muscle-derived cells with hematopoietic potential without otherwise lethal irradiation of muscle donor tissue. We propose to use a unique murine model that relies on the selective and genetically correctable mitomycin C (MMC)-sensitivity of hematopoietic cells in a Fanconi Anemia mouse model. Thus, we will generate functionally chimeric nonlethally irradiated donor animals with a retrovirally corrected, MMC resistant and clonally marked hematopoietic compartment and a non-corrected muscle compartment for a series of transplantation studies. Importantly, our strategy combines a heritable, functionally distinct phenotype of muscle-derived versus marrow-derived hematopoietic progeny with retroviral marking for clonal tracking of engrafted cells. Independent of their developmental origin, the existence of hematopoietically active cells in muscle might conceivably allow the generation of autologous tissues for therapeutic applications with all the implicit advantages over conventional allogeneic grafts. We therefore additionally propose to study the phenotype and investigate the genetic modification of muscle-derived cells responsible for hematopoietic repopulation. Combined with recent insights into the molecular basis of a number of heritable diseases and substantial improvements in the design of vectors to genetically modify and phenotypically correct these cells, this may hold considerable therapeutic potential for the treatment of hereditary marrow failure syndromes including Fanconi Anemia, or as hematopoietic rescue in the context of high-dose therapy for malignancies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21DK063324-02
Application #
6694104
Study Section
Hematology Subcommittee 2 (HEM)
Program Officer
Bishop, Terry Rogers
Project Start
2003-01-01
Project End
2004-12-31
Budget Start
2004-01-01
Budget End
2004-12-31
Support Year
2
Fiscal Year
2004
Total Cost
$173,000
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
078200995
City
Seattle
State
WA
Country
United States
Zip Code
98109
Keyser, Kirsten A; Beagles, Karen E; Kiem, Hans-Peter (2007) Comparison of mesenchymal stem cells from different tissues to suppress T-cell activation. Cell Transplant 16:555-62
Keyser, K A; Morris, J C; Kiem, H-P (2005) Genetically modified CD34+ cells do not contribute to the mesenchymal compartment after autologous transplantation in the baboon. Cytotherapy 7:345-52