Adult human erythroblasts arise from hematopoietic stem cells in the peripheral blood of humans in response to erythropoietin. This process is called erythropoiesis. In many erythroid diseases including hemoglobinopathies, anemia and erythroleukemia, the process of erythropoiesis is abnormal or damaged by the underlying pathology. In order to better understand the molecular mechanisms responsible for these diseases, ex vivo model systems of erythropoiesis were developed using hematopoietic stem cells collected from the peripheral blood of humans. In this study, cells are harvested from peripheral blood and used for ex-vivo assays of erythropoiesis. In addition, collaborative efforts with the department of transfusion medicine are aimed toward improved methods for the collection of hematopoietic stem cells, and specialized methods are being developed for patients with erythroid diseases.

Project Start
Project End
Budget Start
Budget End
Support Year
5
Fiscal Year
2011
Total Cost
$159,040
Indirect Cost
City
State
Country
Zip Code
Tanno, Toshihiko; Miller, Jeffery L (2011) [GDF15 expression and iron overload in ineffective erythropoiesis]. Rinsho Ketsueki 52:387-98
Tanno, Toshihiko; Miller, Jeffery L (2010) Iron Loading and Overloading due to Ineffective Erythropoiesis. Adv Hematol 2010:358283
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Tanno, Toshihiko; Porayette, Prashanth; Sripichai, Orapan et al. (2009) Identification of TWSG1 as a second novel erythroid regulator of hepcidin expression in murine and human cells. Blood 114:181-6
Bhanu, Natarajan V; Lee, Y Terry; Oneal, Patricia A et al. (2008) Inhibition of erythroblast growth and fetal hemoglobin production by ribofuranose-substituted adenosine derivatives. Biochim Biophys Acta 1782:504-10