Abstract
We recently reported on selective interactions between immature T cell subpopulations and bone marrow (BM) stromal cells. To further study this process, we first examined the efficacy of methods estimating cell-cell adhesion and then investigated the effects of cytokines on thymocyte-stroma associations. Techniques based on the use of the fluorochromes calcein- acetomethylester (calcein-AM) and fluorescein diacetate (FDA) were studied and compared to regular cell counting methods. With calcein-AM labeling, the retention time was relatively long, while with FDA labeling, there was a rapid cellular efflux. Using calcein-AM, we developed an accurate quantitative fluorometric assay for determining the adherence of thymocytes to a BM stromal cell line (MBA-13). A maximal fraction of about 29% thymocytes was found to adhere to confluent MBA-13 cell layers after four to six h of coculture. Whereas interleukin 1 did not change the rate of adhesion of thymocytes to the stroma, interferon-γ (IFN-γ) significantly increased adhesion. Basic fibroblast growth factor (bFGF) had a dose-dependent biphasic effect on thymocyte adhesion, and a greater fraction of double negative thymocytes adhered to stroma pretreated with bFGF. Taken together, these results suggest that IFN-γ and bFGF modulate T cells-BM stromal cell adhesion.
Original language | English |
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Pages (from-to) | 229-236 |
Number of pages | 8 |
Journal | Stem Cells |
Volume | 15 |
Issue number | 3 |
DOIs | |
State | Published - 1997 |
Keywords
- Calcein-AM
- FDA
- Fluorimetric cell quantitation
- IFN-γ
- Microenvironment
- T cell-bone marrow stroma cell adhesion
- bFGF