Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/50004
Title: | Prostaglandin E2 and the increase of intracellular cAMP inhibit the expression of interleukin 2 receptors in human T cells | Authors: | Rincón, Mercedes Tugores, Antonio López‐Rivas, Abelardo Silva, Augusto Alonso, Miguel De Landázuri, Manuel O. López‐Botet, Miguel |
UNESCO Clasification: | 32 Ciencias médicas 3205 Medicina interna |
Keywords: | Prostaglandin cAMP Interleukin Human T cells |
Issue Date: | 1988 | Journal: | European Journal of Immunology | Abstract: | We have analyzed the effect mediated by prostaglandin E2 (PGE2) and different reagents that increase intracellular cAMP on the expression of the p55 subunit (CD25) of interleukin 2 receptors (IL2R), on the levels of CD25-specific mRNA and on the expression of high affinity IL 2R. In purified T cells, activated either by an anti-CD3 monoclonal antibody or phytohemagglutinin, the addition of PGE2 (10−6 M), forskolin (5 × 10−5 M), cholera toxin (0.2 μg/ml) or dibutyryl cAMP (dBcAMP) (10−4 M) decreased the cell surface expression of IL 2R by reducing (40%-78% inhibition) the proportions of CD25+ cells as well as the expression of high affinity IL2R, detectable after 24 h. Furthermore, it was observed that PGE2 reduced the concentration of IL2R-specific mRNA after a 6-h period of activation, indicating that its regulatory activity takes place at a pretranslational level. The addition of exogenous recombinant IL2 only partially reversed the inhibition, thus suggesting that PGE2 and increased intracellular concentration of cAMP directly interfered with CD25 expression and that their effect could not be merely attributed to a lack of IL2 dependent positive feedback. Cells cultured under the same conditions in the presence of phorbol myristate acetate, that activates protein kinase C, were refractory to the CAMP-mediated regulation. Finally, we demonstrate that both PGE2 and dBcAMP inhibit the generation of inositol metabolites after T cell activation, thus indicating that these reagents interfere with early signal transduction mechanisms which precede the synthesis of IL2R. | URI: | http://hdl.handle.net/10553/50004 | ISSN: | 0014-2980 | DOI: | 10.1002/eji.1830181121 | Source: | European Journal of Immunology[ISSN 0014-2980],v. 18(11), p. 1791-1796 (Noviembre 1988) |
Appears in Collections: | Artículos |
SCOPUSTM
Citations
137
checked on Dec 8, 2024
WEB OF SCIENCETM
Citations
146
checked on Dec 8, 2024
Page view(s)
50
checked on Oct 5, 2024
Google ScholarTM
Check
Altmetric
Share
Export metadata
Items in accedaCRIS are protected by copyright, with all rights reserved, unless otherwise indicated.