Hematopoietic stem cells are a rare population of cells which have a unique biological profile. This population can be used for cellular therapy of hematological malignancy, bone marrow failure disorders, as well as gene therapy. for more than a decade the CD34 antigen has been used to help isolate this rare population in humans. Transplantation of CD34 positive cells in patients has resulted in prompt engraftment of donor cells. Recently, through the development of antibodies to the CD34 antigen on mouse tissues, it has become possible to study the stem cell biology (i.e., proliferation, differentiation, survival, and self- renewal) using a transplant strategy to determine the importance of CD34 in identifying stem cells. Most stem cell biologists will agree that the stem cell pool is heterogenous with the earliest (highest quality) stem cell having potentials for proliferation, differentiation, survival, and self-renewal but as the stem cell matures these potentials are lost. It becomes critically important in diseases with stem cell intrinsic defects to use the highest quality stem cell for cellular therapy. Recently, conflicting reports have appeared which have made it more difficult to assess functional significance of the CD34 antigen. Our first specific aim will examine the role of CD34 for self-renewal, proliferation, and differentiation. This will involve transplantation of CD34 null stem cells into normal mice and normal cells into null mice to test the competence of these cells in a transplantation protocol. We will also examine the recovery of endogenous stem cells to either radiation or 5-fluorouracil exposure to assess the endogenous competence of CD34 null stem cells.
Specific aim 2 will study the compensatory mechanisms that may be at play in allowing CD34 null mice to survive to adulthood with mildly affected hematopoietic phenotypes. Finally, we will study the homing potential of stem cells from CD34 null mice to engraft normal recipients using a recently developed homing assay in which we will tag stem cells in vivo. We expect that the results of our studies will be directly applicable to treatment of hematological disorders, genetic diseases, and malignancy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK053812-02
Application #
2906189
Study Section
Hematology Subcommittee 2 (HEM)
Program Officer
Badman, David G
Project Start
1998-06-01
Project End
2003-05-31
Budget Start
1999-06-01
Budget End
2000-05-31
Support Year
2
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Krause, D S; Theise, N D; Collector, M I et al. (2001) Multi-organ, multi-lineage engraftment by a single bone marrow-derived stem cell. Cell 105:369-77
Sharkis, S J; Neutzel, S; Collector, M I (2001) Phenotype and function of hematopoietic stem cells. Ann N Y Acad Sci 938:191-4; discussion 194-5
Donnelly, D S; Zelterman, D; Sharkis, S et al. (1999) Functional activity of murine CD34+ and CD34- hematopoietic stem cell populations. Exp Hematol 27:788-96
Lanzkron, S M; Collector, M I; Sharkis, S J (1999) Homing of long-term and short-term engrafting cells in vivo. Ann N Y Acad Sci 872:48-54;discussion 54-6