The process of blood cell formation (hematopoiesis) has been extensively studied but many basic mechanisms continue to be unknown. Previous studies have shown that marrow cell engraftment varies at different points in cell cycle and that these changes are reversible. In recent work we have shown that murine progenitor numbers also vary with cytokine induced cell cycle transit. Studying unseparated marrow cells we demonstrated that 7-factor responsive progenitors (HPP-CFC and CFU-c) increased markedly during the first cell cycle transit and then returned to baseline. Remarkably, these increases were tightly linked to the decreased ability of stem cells to engraft in a competitive transplant model. This phenomenon is termed stem/progenitor cell inversions. These data suggest that the functional phenotype of early marrow stem cells shifts reversibly from engraftable stem cell to progenitor and back to hematopoietic stem cell as it traverses cell cycle, and that the previously conceived stem-cell-to-progenitor unidirectional hierarchy is instead a continuum of reversible phenotypic shifts. The long term objective of this grant are to further characterize the cell cycle related inversions points as to engraftment, progenitor levels and differentiation capacity of the marrow cells studying both unseparated and highly purified stem cells in FLT-3 ligand, thrombopoietin and steel factor. We plan to assess lineage(negative) rhodamine(low) Hoechst(low) (LRH) marrow cells at different points in cell cycle as to short and long-term engraftment in a competititive transplant model, to assess 7-factor-responsive progenitors and to evaluate the capacity of purified stem cells to differentiate in the presence a 7-factor cytokine cocktail and two cocktails designed to promote granulocyte-macrophage or megakaryocyte differentiation. In the engraftment studies there will be an emphasis on G1 phase of cell cycle. The differentiation studies will be carried out in bulk Teflon cultures and on a single cell clonal basis. In order to further understand the phenotype of the stem cell at different points in cell cycle. To point ways to alternative induction studies we will characterize cytokine receptors, adhesion proteins, integrins and other epitopes on the cell surface. These studies employ high-speed cell sorting, fluorescent cell imaging and a variety of in vitro and in vivo stem/progenitor assays. They promise to further define the basic nature of the hematopoietic marrow stem cells and could lead to interesting preclinical models for selective lineage support of various myeloablative therapy approaches .

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08DK064980-04
Application #
7091690
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Bishop, Terry Rogers
Project Start
2003-08-01
Project End
2006-10-31
Budget Start
2006-07-01
Budget End
2006-10-31
Support Year
4
Fiscal Year
2006
Total Cost
$40,406
Indirect Cost
Name
Roger Williams Hospital
Department
Type
DUNS #
625899281
City
Providence
State
RI
Country
United States
Zip Code
02908
Liu, Liansheng; Papa, Elaine F; Dooner, Mark S et al. (2012) Homing and long-term engraftment of long- and short-term renewal hematopoietic stem cells. PLoS One 7:e31300
Colvin, Gerald A; Berz, David; Liu, Liansheng et al. (2010) Heterogeneity of non-cycling and cycling synchronized murine hematopoietic stem/progenitor cells. J Cell Physiol 222:57-65
Dooner, Mark S; Aliotta, Jason M; Pimentel, Jeffrey et al. (2008) Conversion potential of marrow cells into lung cells fluctuates with cytokine-induced cell cycle. Stem Cells Dev 17:207-19
Dooner, Gerri J; Colvin, Gerald A; Dooner, Mark S et al. (2008) Gene expression fluctuations in murine hematopoietic stem cells with cell cycle progression. J Cell Physiol 214:786-95
Colvin, Gerald A; Lambert, Jean-Francois; Dooner, Mark S et al. (2007) Murine allogeneic in vivo stem cell homing(,). J Cell Physiol 211:386-91
Berz, David; McCormack, Elise M; Winer, Eric S et al. (2007) Cryopreservation of hematopoietic stem cells. Am J Hematol 82:463-72
Aliotta, Jason M; Sanchez-Guijo, Fermin M; Dooner, Gerri J et al. (2007) Alteration of marrow cell gene expression, protein production, and engraftment into lung by lung-derived microvesicles: a novel mechanism for phenotype modulation. Stem Cells 25:2245-56
Colvin, Gerald A; Dooner, Mark S; Dooner, Gerri J et al. (2007) Stem cell continuum: directed differentiation hotspots. Exp Hematol 35:96-107
Quesenberry, Peter J; Colvin, Gerald; Abedi, Mehrdad (2005) Perspective: fundamental and clinical concepts on stem cell homing and engraftment: a journey to niches and beyond. Exp Hematol 33:9-19
Quesenberry, Peter J; Dooner, Gerri; Colvin, Gerald et al. (2005) Stem cell biology and the plasticity polemic. Exp Hematol 33:389-94

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