In vivo activation of the interleukin-6 receptor/gp130 signaling pathway in pituitary corticotropes of lipopolysaccharide-treated rats

被引:17
作者
Gautron, L [1 ]
Lafon, P [1 ]
Tramu, G [1 ]
Layé, S [1 ]
机构
[1] Univ Bordeaux 1, Lab Regulat Neuroendocriniennes, F-33405 Talence, France
关键词
proopiomelanocortin; in situ hybridization; immunocytochemistry; STAT-3; Fos; lipopolysaccharide; interleukins; inflammation; neuroimmune interactions; corticotropes;
D O I
10.1159/000068336
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adrenocorticotropic hormone (ACTH) release from anterior pituitary corticotropes is greatly increased during peripheral inflammation induced by lipopolysaccharide (LPS) administration. Interleukin-6 (IL-6) is thought to participate in LPS-induced ACTH release, but whether or not corticotropes are directly targeted by this cytokine is unclear. Therefore, we investigated the expression and activation of IL-6 signaling components in the pituitary of rats 2 and 4 h after administration of LPS (250 mug/kg). Intraperitoneal LPS treatment provoked the nuclear translocation of signal transducer and activator of transcription 3 (STAT-3) and Fos expression in the anterior pituitary lobe, as demonstrated by immunohistochemistry. By using in situ hybridization, we demonstrated that suppressor of cytokine signaling 3 (SOCS-3) and c-fos mRNAs were significantly induced by the LPS treatment in the anterior lobe of the pituitary. Dual in situ hybridization revealed that most corticotropes expressed IL-6 receptor and gp130 mRNAs, and that 2 h after LPS treatment, SOCS-3 and c-fos mRNAs were induced in corticotropes. Our results suggest that LPS-induced IL-6 could regulate the hypothalamo-pituitary-adrenal axis by directly targeting corticotropes during peripheral inflammation. Copyright (C) 2003 S. Karger AG, Basel.
引用
收藏
页码:32 / 43
页数:12
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