The long term objective of this research proposal is to increase our knowledge in physiological interrelationships between hemopoietic tissue and bone tissue, seeking a possible role of hemopoietic cells in regulation of bone turnover. Using an animal del of tumor-induced granulocytosis associated with hypercalcemia, and isolating the more derived humoral factors, the mechanisms of bone resorption in hyperplastic bone arrow will be explored. During the next grant period, the investigation of bone cell stimulating and bone resorbing humoral agents demonstrated from the CE mammary carcinoma cell clones will be investigated for their molecular relationships to granulopoieticc growth factors also elaborated from the tumor, by the use of molecular probes, well as specific antisera of hemopoietic growth factors, conventional biochemical purification procedures and analysis of gene expression. A new method to precisely analyses osteoclast progenitors from the bone marrow in vitro will be established, characterized and utilized for assays of bone resorbing activities. The in vivo function of isolated CE tumor derived bone modulating or granulopoietic factor will be tested in vivo for its ability to care osteopetrosis in mice. The role of the CE mammary carcinoma- derived factor as well as various purified hemopoietic growth factors in bone resorbing process will be explored by in vitro culture experiments using isolated bone forming cells, marrow stromal cells, marrow mononuclear cells and bone particles and the mechanism of growth factor mediated bone resorotion will be dissected. These studies are to disclose many unanswered basic questions about the defect of hemopoietic growth factors on physiology of bone marrow and bone turnover; well as to understand pathophysiology of unexplained hypercalcemia associated with certain tumors.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA038189-05
Application #
3176257
Study Section
Hematology Subcommittee 2 (HEM)
Project Start
1984-06-15
Project End
1992-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
5
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
Schools of Medicine
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Lee, M Y; Fevold, K L; Muguruma, Y et al. (1997) Conditions that support long-term production of osteoclast progenitors in vitro. Stem Cells 15:340-6
Hayase, Y; Muguruma, Y; Lee, M Y (1997) Osteoclast development from hematopoietic stem cells: apparent divergence of the osteoclast lineage prior to macrophage commitment. Exp Hematol 25:19-25
Lee, M Y; Jonas, M; Lottsfeldt, J L et al. (1996) Ultrastructural characterization of preosteoclasts derived from bone marrow progenitors stimulated by osteoclast colony stimulating factor. Anat Rec 246:176-84
Lee, T H; Fevold, K L; Muguruma, Y et al. (1994) Relative roles of osteoclast colony-stimulating factor and macrophage colony-stimulating factor in the course of osteoclast development. Exp Hematol 22:66-73
Povolny, B T; Lee, M Y (1993) The role of recombinant human M-CSF, IL-3, GM-CSF and calcitriol in clonal development of osteoclast precursors in primate bone marrow. Exp Hematol 21:532-7
Lee, M Y; Fevold, K L; Dorshkind, K et al. (1993) In vivo and in vitro suppression of primary B lymphocytopoiesis by tumor-derived and recombinant granulocyte colony-stimulating factor. Blood 82:2062-8
Lee, M Y; Lottsfeldt, J L; Fevold, K L (1992) Identification and characterization of osteoclast progenitors by clonal analysis of hematopoietic cells. Blood 80:1710-6
Lee, M Y; Fukunaga, R; Lee, T J et al. (1991) Bone modulation in sustained hematopoietic stimulation in mice. Blood 77:2135-41
Lee, M Y; Eyre, D R; Osborne, W R (1991) Isolation of a murine osteoclast colony-stimulating factor. Proc Natl Acad Sci U S A 88:8500-4
Povolny, B; Lee, M; Hall, S (1990) Modulation of tartrate-resistant acid phosphatase expression by calcitriol in CSF-induced macrophage colonies. Exp Hematol 18:283-8

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