Poorly liver metastatic large-cell lymphoma RAWll7.P cells were sequentially selected in vitro for increased adhesion to murine hepatic sinusoidai endothelial cells. After three or four sequential selections, the selected sublines showed increased rates of adhesion to target hepatic microvessel endo
Modulating the metastatic potential of murine raw117 large-cell lymphoma cells by selection for resistance to interferon-γ
✍ Scribed by Ronald A. Labiche; Garth L. Nicolson
- Book ID
- 102868889
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 919 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Highly metastatic, in vivo-selected cells of RAW I 17-H I0 large-cell lymphoma have been shown to be more resistant than poorly metastatic parental RAW I 17-P cells to the cytolytic and cytostatic activities of activated macrophages in co-culture experiments. Activated macrophages are known to produce soluble, cytostatic respiration-inhibiting factors, and such activities can be duplicated by interferon-gamma (IFN-y) or by combinations of I F N y and Escherichio coli lipopolysaccharide (LPS). Highly metastatic RAW I 17-H I0 cells are more resistant to the cytostatic effects of IFN-y and LPS than poorly metastatic
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