The study of lineage specification during hematopoiesis in mammals is important due to its relationship to many blood related disorders including Leukemia. However, many fundamental questions regarding the specification of unique fates remain unresolved. Drosophila has a simple hematopoietic system constituting of cell types that function in innate immunity and phagocytosis. A hierarchy of multiple transcription factors that specify hematopoietic lineage in Drosophila have been identified. The GATA factor Serpent is required for all hematopoiesis. Lozenge, which bears similarity to the Acute Myeloid Leukemia protein in humans is required for the development of one blood cell type, the crystal cells in Drosophila. Gcm is required for the development of the plasmatocytes/macrophages. Recently we have established that the Notch receptor and its ligand Serrate are involved in the induction of blood cells in Drosophila. In this proposal, we present a comprehensive analysis of Drosophila hematopoiesis. The role of Serpent in larval hematopoiesis will be studied; the involvement of the Notch pathway in blood cell development will be fully analyzed. The hematopoietic precursor population will be characterized. A comprehensive genetic study will be performed for a possible role of the many known signal transduction cascades in the process of hematopoieis. Finally, genetic screens will identify genes that are involved in Drosophila hematopoiesis. Given the similarity of the known members of this developmental system with proteins with important function in mammalian hematopoiesis, we expect that many of the new genes identified will have relevance to this important developmental process in mammals.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL067395-01
Application #
6322995
Study Section
Special Emphasis Panel (ZRG1-SSS-Y (02))
Program Officer
Thomas, John
Project Start
2001-05-10
Project End
2005-04-30
Budget Start
2001-05-10
Budget End
2002-04-30
Support Year
1
Fiscal Year
2001
Total Cost
$363,896
Indirect Cost
Name
University of California Los Angeles
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Cho, Bumsik; Spratford, Carrie M; Yoon, Sunggyu et al. (2018) Systemic control of immune cell development by integrated carbon dioxide and hypoxia chemosensation in Drosophila. Nat Commun 9:2679
Mondal, Bama Charan; Shim, Jiwon; Evans, Cory J et al. (2014) Pvr expression regulators in equilibrium signal control and maintenance of Drosophila blood progenitors. Elife 3:e03626
Evans, Cory J; Liu, Ting; Banerjee, Utpal (2014) Drosophila hematopoiesis: Markers and methods for molecular genetic analysis. Methods 68:242-51
Grigorian, Melina; Liu, Ting; Banerjee, Utpal et al. (2013) The proteoglycan Trol controls the architecture of the extracellular matrix and balances proliferation and differentiation of blood progenitors in the Drosophila lymph gland. Dev Biol 384:301-12
Shim, Jiwon; Mukherjee, Tina; Mondal, Bama Charan et al. (2013) Olfactory control of blood progenitor maintenance. Cell 155:1141-53
Honti, Viktor; Cinege, Gyöngyi; Csordás, Gábor et al. (2013) Variation of NimC1 expression in Drosophila stocks and transgenic strains. Fly (Austin) 7:263-6
Shim, Jiwon; Mukherjee, Tina; Banerjee, Utpal (2012) Direct sensing of systemic and nutritional signals by haematopoietic progenitors in Drosophila. Nat Cell Biol 14:394-400
Mondal, Bama Charan; Mukherjee, Tina; Mandal, Lolitika et al. (2011) Interaction between differentiating cell- and niche-derived signals in hematopoietic progenitor maintenance. Cell 147:1589-600
Mukherjee, Tina; Kim, William Sang; Mandal, Lolitika et al. (2011) Interaction between Notch and Hif-alpha in development and survival of Drosophila blood cells. Science 332:1210-3
Sinenko, Sergey A; Shim, Jiwon; Banerjee, Utpal (2011) Oxidative stress in the haematopoietic niche regulates the cellular immune response in Drosophila. EMBO Rep 13:83-9

Showing the most recent 10 out of 20 publications