Decades of research into the cellular and molecular mechanisms of hematopoietic stem cell (HSC) maintenance, proliferation, and differentiation have led to volumes of information about the hematopoietic stem cell. Despite this extensive knowledge, the identity of cells and cell products that provide the extrinsic control of HSC fate remain largely unknown, but are attributed to cells and cell products of the bone marrow microenvironment (ME). A Novel 3D culture system incorporating cells suspended in a matrix together with endothelial lined vessels provides a new way to interrogate cell interactions within the complex ME. Utilizing well characterized stromal cell lines that are functionally distinct, we will build a 3D ME to mimic the signaling thought to occur via cell to cell interactions in vivo. W will then introduce gene modified CD34+ cells transduced with a mCherry gene under the control of the megakaryocyte lineage specific promoter PF-4 to detect lineage commitment in these cells. Once the commitment assay is standardized, we will test the hypothesis that monocytes in contact with stromal cells play a critical role in defining the functionality of the M, particularly as it relates to sustaining the uncommitted state. We anticipate that monocytes together with specific stromal cells will provide signals that function to prevent commitment. To test the function of the non GFP+ and presumably uncommitted cells, we will remove the cells from the cultures and test their ability to produce multi-lineage progeny in expansion cultures and NOD/SCID assays. If we can demonstrate the maintenance of multi-potentiality, with or without cell division, future studies can use knockdown techniques to identify the pathways involved.

Public Health Relevance

Understanding how blood cell production is regulated would allow us to develop therapies to control it. Progress has been made to the extent that scientists have identified several cell types that occupy the marrow microenvironment and provide required signals that control stem cell fate. We do not know how these components work together spatially or temporally to affect this regulation. The 3-dimensional model proposed in this application will allow these questions to be addressed.

National Institute of Health (NIH)
Postdoctoral Individual National Research Service Award (F32)
Project #
Application #
Study Section
Special Emphasis Panel (ZDK1)
Program Officer
Bishop, Terry Rogers
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
Fred Hutchinson Cancer Research Center
United States
Zip Code