Interleukin-1β enhances interleukin-1 receptor antagonist content in human somatotroph adenoma cell cultures
In addition to the well-known modulation of immune and inflammatory responses, the interleukin-1 (IL-1) system has been shown to be involved in the regulation of anterior pituitary hormone secretion and growth. We previously demonstrated that IL-1 receptor antagonist (IL-1ra) is expressed in human p...
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Autores principales: | , , , , , , , , |
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Formato: | JOUR |
Materias: | |
Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_0021972X_v83_n7_p2429_Sauer |
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Sumario: | In addition to the well-known modulation of immune and inflammatory responses, the interleukin-1 (IL-1) system has been shown to be involved in the regulation of anterior pituitary hormone secretion and growth. We previously demonstrated that IL-1 receptor antagonist (IL-1ra) is expressed in human pituitary adenomas cultured in vitro. In the present study, we investigated the regulation of IL-1ra protein by IL-1β (1-100 U/mL) in human somatotroph adenomas (n = 9) cultured for 12-48 h. IL-1β significantly enhanced the concentration of IL-1ra dose dependently in the somatotroph adenoma cell lysates, whereas IL-1ra concentrations remained unchanged in the culture supernatants. Furthermore, basal IL-1ra concentrations were significantly higher in the cell lysates compared with the corresponding culture supernatants. The regulation of IL-1ra in somatotroph adenoma cells is different from human cultured monocytes, in which IL-1β significantly stimulated IL-1ra secretion into the culture supernatants, and no change of intracellular IL-1ra content was observed. Incubation of the somatotroph adenoma cells with 100 U/mL IL-1β did not result in a change of GH concentrations in the culture supernatants. Enhancement of intracellular IL- 1ra protein by IL-1β may represent a mechanism intrinsic to somatotroph adenoma cells to counterregulate the response to IL-1β on hormone secretion or cellular growth. |
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