Large numbers of B lymphocytes are produced within bone marrow throughout life, constantly replenishing the humoral immune system. It is important to understand how this process is controlled and experiments with mice suggest that two categories of steroid hormones have important roles. Hormone withdrawal through castration, mutation or adrenalectomy increases lymphopoietic activity while experimental treatment with estrogen or glucocorticoids selectively suppresses lymphocyte formation in marrow. There is unfortunately little information about long- range consequences for humans who are deliberately or environmentally exposed to many related compounds. Until recently, it has been difficult to identify the cellular targets of these hormones and perform meaningful studies of molecular mechanisms. However, there have been steady improvements in resolution and sorting of rare subsets of marrow precursors, as well as defined conditions for their propagation in culture. The result is that we now have much better insight into early differentiation pathways through which stem cells give rise to precursors of B, T and NK cells. Several findings suggest that these lineages diverge from myeloid and erythroid progenitors at, or just before, a hormone sensitive stage. Ongoing studies will clarify when such lineage fate decisions are made and reveal how hormones selectively influence them. While steroid hormones can regulate stromal cells within bone marrow, it is now clear that rare early lymphocyte precursors are also direct targets. Ongoing studies will investigate what hormone receptors are utilized and molecular consequences of receptor ligation. Surprisingly, the immune system develops during embryonic life although estrogen levels are high and sufficient to suppress lymphocyte formation in maternal bone marrow. This may now be explained by developmentally dependent control of sex steroid receptors. The first appearance of these receptors on neonatal hematopoietic cells will be carefully documented and environmental control of this process investigated. The studies are providing basic information about lymphocyte production that should ultimately help understand, manage and cure immunodeficiency, autoimmune and malignant diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI020069-21
Application #
6621175
Study Section
Immunobiology Study Section (IMB)
Program Officer
Nasseri, M Faraz
Project Start
1982-09-01
Project End
2006-11-30
Budget Start
2002-12-01
Budget End
2003-11-30
Support Year
21
Fiscal Year
2003
Total Cost
$392,250
Indirect Cost
Name
Oklahoma Medical Research Foundation
Department
Type
DUNS #
077333797
City
Oklahoma City
State
OK
Country
United States
Zip Code
73104
Welner, Robert S; Kincade, Paul W (2014) 9-1-1: HSCs respond to emergency calls. Cell Stem Cell 14:415-6
Iida, Ryuji; Welner, Robert S; Zhao, Wanke et al. (2014) Stem and progenitor cell subsets are affected by JAK2 signaling and can be monitored by flow cytometry. PLoS One 9:e93643
Zhang, Qingzhao; Esplin, Brandt L; Iida, Ryuji et al. (2013) RAG-1 and Ly6D independently reflect progression in the B lymphoid lineage. PLoS One 8:e72397
Satoh, Yusuke; Yokota, Takafumi; Sudo, Takao et al. (2013) The Satb1 protein directs hematopoietic stem cell differentiation toward lymphoid lineages. Immunity 38:1105-15
Zhang, Qingzhao; Iida, Ryuji; Yokota, Takafumi et al. (2013) Early events in lymphopoiesis: an update. Curr Opin Hematol 20:265-72
Ichii, Michiko; Frank, Mark Barton; Iozzo, Renato V et al. (2012) The canonical Wnt pathway shapes niches supportive of hematopoietic stem/progenitor cells. Blood 119:1683-92
Shimazu, Tomoyuki; Iida, Ryuji; Zhang, Qingzhao et al. (2012) CD86 is expressed on murine hematopoietic stem cells and denotes lymphopoietic potential. Blood 119:4889-97
Zhang, Qingzhao; Iida, Ryuji; Shimazu, Tomoyuki et al. (2012) Replenishing B lymphocytes in health and disease. Curr Opin Immunol 24:196-203
Luis, T C; Ichii, M; Brugman, M H et al. (2012) Wnt signaling strength regulates normal hematopoiesis and its deregulation is involved in leukemia development. Leukemia 26:414-21
Esplin, Brandt L; Shimazu, Tomoyuki; Welner, Robert S et al. (2011) Chronic exposure to a TLR ligand injures hematopoietic stem cells. J Immunol 186:5367-75

Showing the most recent 10 out of 136 publications