The overall goals of the proposal are to better understand how feline leukemia virus (FeLV) results in selective erythroid marrow failure and how normal and neoplastic stem cells interact in the evolution of virus-induced myelodysplasia or leukemia. Further studies are outlined to define the mechanisms underlying pure red cell aplasia (PRCA) in cats infected with FeLV-C/Sarma. In order to study the clonal evolution of hematologic diseases prior to clinically evident neoplasia, we have developed a unique G-6-PD heterozygous cat model. Using this model we will study the evolution of myeloproliferative diseases and leukemia in animals infected with FeLV-AB/GM-1 or FeLV-B/Gardner Arnstein. Infection of hematopoietic cells will be carried out both in vivo and in long-term marrow culture to assess the behavior of normal versus transformed and presumably neoplastic stem cells. Furthermore, we will construct a virus combining FeLV-C and the erb-B oncogene. We predict that erythroleukemia will develop in infected animals. Finally, using the G-6-PD heterozygous model, we will study issues of clonal succession and cycling in cats supported by relatively few stem cells. This model will be generated through the repeated use of myelosuppressive drugs such as dimethylmyleran or through autologous bone marrow transplantation employing low numbers of hematopoietic cells.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
2R01HL031823-04
Application #
3343023
Study Section
Hematology Subcommittee 2 (HEM)
Project Start
1986-12-01
Project End
1991-11-30
Budget Start
1986-12-01
Budget End
1987-11-30
Support Year
4
Fiscal Year
1987
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
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Philip, Mary; Chiu, Edison Y; Hajjar, Adeline M et al. (2016) TLR Stimulation Dynamically Regulates Heme and Iron Export Gene Expression in Macrophages. J Immunol Res 2016:4039038
Doty, Raymond T; Phelps, Susan R; Shadle, Christina et al. (2015) Coordinate expression of heme and globin is essential for effective erythropoiesis. J Clin Invest 125:4681-91
Keel, Siobán B; Doty, Raymond; Liu, Li et al. (2015) Evidence that the expression of transferrin receptor 1 on erythroid marrow cells mediates hepcidin suppression in the liver. Exp Hematol 43:469-78.e6
Philip, Mary; Funkhouser, Scott A; Chiu, Edison Y et al. (2015) Heme exporter FLVCR is required for T cell development and peripheral survival. J Immunol 194:1677-85
Egan, Daniel N; Yang, Zhantao; Phillips, John et al. (2015) Inducing iron deficiency improves erythropoiesis and photosensitivity in congenital erythropoietic porphyria. Blood 126:257-61
Byon, John C H; Chen, Jing; Doty, Raymond T et al. (2013) FLVCR is necessary for erythroid maturation, may contribute to platelet maturation, but is dispensable for normal hematopoietic stem cell function. Blood 122:2903-10
Keel, Sioban B; Phelps, Susan; Sabo, Kathleen M et al. (2012) Establishing Rps6 hemizygous mice as a model for studying how ribosomal protein haploinsufficiency impairs erythropoiesis. Exp Hematol 40:290-4
Hromas, Robert; Abkowitz, Janis L; Keating, Armand (2012) Facing the NIH funding crisis: how professional societies can help. JAMA 308:2343-4
Jaacks, Lindsay M; Young, Melissa F; Essley, Bridget V et al. (2011) Placental expression of the heme transporter, feline leukemia virus subgroup C receptor, is related to maternal iron status in pregnant adolescents. J Nutr 141:1267-72

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