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Título: | Interleukin (IL)-2 activation of p21ras in murine myeloid cells transfected with human IL-2 receptor ß chain |
Autor: | Izquierdo, Manuel CSIC ORCID ; Downward, Julian; Otani, Hiroki; Leonard, Warren J.; Cantrell, Doreen A. | Fecha de publicación: | 1992 | Editor: | Wiley-VCH | Citación: | European Journal of Immunology 22(3): 817-821 (1992) | Resumen: | The T cell growth factor interleukin-2 (IL-2) induces p21ras activation in T lymphocytes. To determine whether the IL-2 receptor (IL-2R) can regulate p21ras when expressed in a non-T cell environment we have examined the ability of IL-2 to activate p21ras in 32D murine myeloid progenitor cells transduced with human IL-2R ß chains. These cells are denoted ß53 cells. 32D cells normally proliferate in response to IL-3 but the expression of the IL-2R ß chain confers IL-2 responsiveness to the cells. Our data show that IL-3 is able to activate p21ras in the parental 32D cells and both IL-2 and IL-3 can stimulate p21ras in the IL-2R-expressing ß53 clone of 32D. In T lymphocytes, activation of protein kinase C (PKC) with phorbol esters is sufficient to stimulate p21ras. However, in 32D and ß53 cells activation of PKC with phorbol esters does not result in p21ras activation even though these cells express functional PKC It appears, therefore, that a PKC-mediated pathway for p21ras regulation exists in T lymphocytes but not in 32D cells. The IL-2R can couple to p21ras independently of the concomitant presence of the PKC pathway for p21ras regulation. These data imply that multiple intracellular mechanisms may exist to regulate p21ras and that cells of different lineages may differ with regard to p21ras regulation. | URI: | http://hdl.handle.net/10261/160282 | DOI: | 10.1002/eji.1830220328 | Identificadores: | doi: 10.1002/eji.1830220328 issn: 0014-2980 e-issn: 1521-4141 |
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