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Involvement of Corticotropin-Releasing Hormone- and Interleukin (IL)-6-Dependent Proopiomelanocortin Induction in the Anterior Pituitary during Hypothalamic-Pituitary-Adrenal Axis Activation by IL-1α
Author(s) -
Dai Chida,
Toshihiro Imaki,
Toshihiro Suda,
Yoichiro Iwakura
Publication year - 2005
Publication title -
endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/en.2005-0409
Subject(s) - proopiomelanocortin , endocrinology , medicine , anterior pituitary , corticotropic cell , pituitary gland , corticotropin releasing hormone , hormone , hypothalamic–pituitary–adrenal axis , interleukin 1β , adrenocorticotropic hormone , peptide hormone , hypopituitarism , interleukin , cytokine
IL-1α/β and IL-6 are endogenous modulator of hypothalamo-pituitary-adrenal axis (HPAA) and are thought to play key roles in immune-neuroendocrine interactions during inflammation. Here, we show IL-1α induced a normal HPAA activation in IL-1α/β knockout (KO) and IL-6 KO mice at 1 h; however, at 6 h HPAA activation was reduced relative to wild-type mice, indicating a role for endogenous IL-1α/β and IL-6 in prolonged HPAA activation. We found that the induction of proopiomelanocortin (POMC) transcript in the anterior pituitary (AP) at 6 h in response to IL-1α was reduced in IL-1α/β KO and IL-6 KO mice, as well as in CRH KO mice, suggesting IL-1α/β, IL-6, and CRH are all required for POMC induction. The induction of CRH transcript in the paraventricular nucleus at 6 h and plasma IL-6 levels, in response to IL-1α, were reduced in IL-1α/β KO mice. Because IL-1α-induced activation of signal transducer and activator of transcription 3 in the AP was also suppressed in IL-6 KO mice, we suggest that plasma IL-6 is first induced by IL-1α, and IL-6 activates signal transducer and activator of transcription 3 in the AP, leading to the induction of POMC in concert with CRH. Our results suggest a role for IL-1α/β in the induction of POMC in the AP through the induction of two independent pathways, CRH and IL-6.

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