Journal
EXPERIMENTAL HEMATOLOGY
Volume 34, Issue 12, Pages 1730-1740Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.exphem.2006.08.001
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Funding
- NIDDK NIH HHS [R01 DK057899, R56 DK057899, DK57899] Funding Source: Medline
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Objective. The OP9-DL1 culture system is an in vitro model for T-cell development in which activation of the Notch pathway by Delta-like I promotes differentiation of mature T cells from progenitors. The roles of specific cytokines in this culture system have not been well defined, and controversy regarding the role of IL-7 has recently emerged. We examined the roles played by IL-7, Flt3 ligand, and stem cell factor (SCF) in differentiation of adult bone marrow cells in the OP9-DL1 culture system. Methods. Hematopoietic progenitor cells isolated from mouse bone marrow were cultured with OP9 or OP9-DL1 stromal cells and evaluated for T and B lymphocyte differentiation using immunofluorescent staining. Results. IL-7 provided both survival/proliferation and differentiation signals in a dose-dependent manner. T-cell development from the CD4/CD8 double-negative (DN) stage to the CD4/CD8 double-positive (D]P) stage required IL-7 provided by the stromal cells, while differentiation from the DP to the CD8 single-positive (SP) stage required addition of exogenous IL-7. SCF favored the proliferation of DN lymphoid progenitors and inhibited differentiation to the DP stage in a dose-dependent manner. Conversely, blocking the function of SCF expressed endogenously by OP9-DL1 cells inhibited proliferation of lymphoid progenitors and accelerated T-lineage differentiation. Flt3 ligand promoted proliferation without affecting differentiation. \ Conclusion. These results validate the OP9-DL1 model for the analysis of T-cell development from bone marrow-derived progenitor cells, and demonstrate specific roles of SCF, IL-7, and Flt3L in promoting efficient T-lineage differentiation. (c) 2006 International Society for Experimental Hematology. Published by Elsevier Inc.
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