Hematopoietic stem cells are a rare population of cells which have the unique potential to aid cellular therapy for hematological malignancies, bone marrow failure disorders, as well as gene therapy. These cells are most commonly isolated using the CD34 antigen. CD34 is expressed specifically by these cells, but its function is unknown. Whether CD34 function plays a role in stem cell biology is an important question. Furthermore, CD34 expression on the earliest stem cell remains uncertain, although it is well-documented that more mature stem cells express CD34. However, it may be critically important in diseases with stem cell intrinsic defects to use the most primitive stem cell for cellular therapy. Our first specific aim will examine the role for CD34 expression for self-renewal, proliferation, and differentiation of primitive stem cells. This will involve transplantation of CD34 null stem cells into normal mice and normal cells into null mice to test the competence of these null cells. In this setting we will also examine the recovery of endogenous CD34 null stem cells to either radiation of 5-fluorouracil exposure.
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. Specifically, cells present in the normal thymus have been shown to support or inhibit hematopoiesis. We will determine if these thymic cells in CD34 null mice provide the same functions. In this aim we will also 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.
In specific aim 3 will decipher the mechanism by which CD34 blocks the differentiation of hematopoietic cells. We will identify protein(s) which interact with the important regulatory domain within the intracellular region of the CD34 molecule that may negatively control differentiation. 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 Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA070970-03
Application #
6300501
Study Section
Project Start
2000-04-01
Project End
2001-03-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
3
Fiscal Year
2000
Total Cost
$244,288
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Gamper, Christopher J; Takemoto, Clifford M; Chen, Allen R et al. (2016) High-dose Cyclophosphamide is Effective Therapy for Pediatric Severe Aplastic Anemia. J Pediatr Hematol Oncol 38:627-635
Fox, Jennifer M; Moynihan, James R; Mott, Bryan T et al. (2016) Artemisinin-derived dimer ART-838 potently inhibited human acute leukemias, persisted in vivo, and synergized with antileukemic drugs. Oncotarget 7:7268-79
Sharrow, Allison C; Perkins, Brandy; Collector, Michael I et al. (2016) Characterization of aldehyde dehydrogenase 1 high ovarian cancer cells: Towards targeted stem cell therapy. Gynecol Oncol 142:341-8
Kim, MinJung; Tan, Yee Sun; Cheng, Wen-Chih et al. (2015) MIR144 and MIR451 regulate human erythropoiesis via RAB14. Br J Haematol 168:583-97
Candia, Julián; Cherukuri, Srujana; Guo, Yin et al. (2015) Uncovering low-dimensional, miR-based signatures of acute myeloid and lymphoblastic leukemias with a machine-learning-driven network approach. Converg Sci Phys Oncol 1:
Brodsky, Robert A (2014) Paroxysmal nocturnal hemoglobinuria. Blood 124:2804-11
Rau, Rachel; Magoon, Daniel; Greenblatt, Sarah et al. (2014) NPMc+ cooperates with Flt3/ITD mutations to cause acute leukemia recapitulating human disease. Exp Hematol 42:101-13.e5
Tan, Yee Sun; Kim, MinJung; Kingsbury, Tami J et al. (2014) Regulation of RAB5C is important for the growth inhibitory effects of MiR-509 in human precursor-B acute lymphoblastic leukemia. PLoS One 9:e111777
Ma, Hayley S; Nguyen, Bao; Duffield, Amy S et al. (2014) FLT3 kinase inhibitor TTT-3002 overcomes both activating and drug resistance mutations in FLT3 in acute myeloid leukemia. Cancer Res 74:5206-17
Belet, Stefanie; Fieremans, Nathalie; Yuan, Xuan et al. (2014) Early frameshift mutation in PIGA identified in a large XLID family without neonatal lethality. Hum Mutat 35:350-5

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