Dr. Srour proposes to examine the relationship between cell cycle progression and cell division of hematopoietic stem cells (HSC) and maintenance of fundamental function of these cells. During the previous funding period, he gained insight into the association between mitotic quiescence and HSC function and correlated several biological properties of these cells with their position in the cell cycle. He documented a decline in hematopoietic potential as dormant CD34+ cells traversed from G0 into G1 in the absence of cell division and illustrated the existence of a hierarchical organization of HSC relative to their responsiveness to cytokine stimulation. Strategies delivering efficient retroviral mediated gene transduction and long-term expression of transduced genes were formulated. Although Dr. Srour gained valuable information by meeting or exceeding all of the specific aims of the original proposal, more remains to be learned. The relevance of mitotic quiescence of HSC to their functional potential during embryonic development is yet to be explored. Dr. Srour contends that it remains to be established whether HSC fate is intrinsically or extrinsically regulated. To better understand these critical issues in stem cell biology, three specific aims will be examined. First, Dr. Srour will test whether during embryonic development, non-cycling, as well as HSC in active phases of the cell cycle, are equally effective in engrafting and sustaining long-term hematopoiesis. He hypothesizes that the extensive need for hematopoietic cells during fetal development obligates resting and cycling HSC to contribute to blood cell production while maintaining the stem cell pool. Second, he will investigate if recruitment of dormant HSC into active phases of the cell cycle and subsequent self-renewal divisions are intrinsically or extrinsically regulated. Third, he will use information gleaned from the first and second specific aims to improve the transduction efficiency of foreign genetic material into HSC using retroviral mediated gene transfer.
These specific aims should yield valuable information about normal hematopoiesis and the mechanisms that regulate stem cell fate. Information gained from these studies will be important for understanding the roles of cell cycle activation and proliferation in maintaining the hematopoietic potential of HSC throughout ontogeny, and for proper utilization of HSC in transplantation, ex vivo expansion, and gene therapy.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL055716-06
Application #
6389548
Study Section
Hematology Subcommittee 2 (HEM)
Program Officer
Thomas, John
Project Start
1995-09-30
Project End
2004-06-30
Budget Start
2001-07-01
Budget End
2002-06-30
Support Year
6
Fiscal Year
2001
Total Cost
$223,500
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
005436803
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
Hooker, R A; Chitteti, B R; Egan, P H et al. (2015) Activated leukocyte cell adhesion molecule (ALCAM or CD166) modulates bone phenotype and hematopoiesis. J Musculoskelet Neuronal Interact 15:83-94
Cheng, Ying-Hua; Streicher, Drew A; Waning, David L et al. (2015) Signaling pathways involved in megakaryocyte-mediated proliferation of osteoblast lineage cells. J Cell Physiol 230:578-86
Wang, Lin; Zhang, Huajia; Rodriguez, Sonia et al. (2014) Notch-dependent repression of miR-155 in the bone marrow niche regulates hematopoiesis in an NF-?B-dependent manner. Cell Stem Cell 15:51-65
Chitteti, Brahmananda Reddy; Kobayashi, Michihiro; Cheng, Yinghua et al. (2014) CD166 regulates human and murine hematopoietic stem cells and the hematopoietic niche. Blood 124:519-29
Chitteti, Brahmananda R; Cheng, Ying-Hua; Kacena, Melissa A et al. (2013) Hierarchical organization of osteoblasts reveals the significant role of CD166 in hematopoietic stem cell maintenance and function. Bone 54:58-67
Bethel, Monique; Chitteti, Brahmananda R; Srour, Edward F et al. (2013) The changing balance between osteoblastogenesis and adipogenesis in aging and its impact on hematopoiesis. Curr Osteoporos Rep 11:99-106
Cheng, Ying-Hua; Hooker, R Adam; Nguyen, Khanh et al. (2013) Pyk2 regulates megakaryocyte-induced increases in osteoblast number and bone formation. J Bone Miner Res 28:1434-45
Chitteti, Brahmananda Reddy; Bethel, Monique; Voytik-Harbin, Sherry L et al. (2013) In vitro construction of 2D and 3D simulations of the murine hematopoietic niche. Methods Mol Biol 1035:43-56
Chitteti, Brahmananda R; Bethel, Monique; Kacena, Melissa A et al. (2013) CD166 and regulation of hematopoiesis. Curr Opin Hematol 20:273-80
Culang-Reinlieb, Michelle E; Sneed, Joel R; Keilp, John G et al. (2012) Change in cognitive functioning in depressed older adults following treatment with sertraline or nortriptyline. Int J Geriatr Psychiatry 27:777-84

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