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白细胞介素-11刺激促肾上腺皮质激素细胞中阿黑皮素原基因表达及促肾上腺皮质激素分泌:下丘脑-垂体-肾上腺轴中细胞因子冗余网络的证据

Interleukin-11 stimulates proopiomelanocortin gene expression and adrenocorticotropin secretion in corticotroph cells: evidence for a redundant cytokine network in the hypothalamo-pituitary-adrenal axis.

作者信息

Auernhammer C J, Melmed S

机构信息

Cedars-Sinai Research Institute, UCLA School of Medicine, Los Angeles, California 90048, USA.

出版信息

Endocrinology. 1999 Apr;140(4):1559-66. doi: 10.1210/endo.140.4.6636.

Abstract

We recently characterized leukemia inhibitory factor (LIF) as an important modulator of hypothalamo-pituitary-adrenal (HPA) axis activity. We now describe the role of interleukin (IL)-11, another member of the IL-6 cytokine family, in the neuro-immuno-endocrine modulation of the HPA axis. In murine hypothalamus, pituitary and corticotroph AtT-20 cells, IL-11 messenger RNA (mRNA) was detectable by RT-PCR only, whereas IL-11R mRNA transcripts were demonstrated by Northern blot. Using RT-PCR, IL-11 and IL-11R gene expression were also detected in normal human pituitaries, as well as in corticotropic and nonfunctioning pituitary adenomas. Incubation of AtT-20 cells for 24 h with 10(-9) M IL-11 stimulated ACTH secretion 1.4 +/- 0.1-fold (P < 0.01), whereas LIF at the same concentration caused a 1.5 +/- 0.1-fold increase (P < 0.001). POMC mRNA expression was induced by IL-11 (0.5 x 10(-9) M) and LIF (0.5 x 10(-9) M) 1.5 +/- 0.18-fold (P < 0.05) and 1.7 +/- 0.13-fold (P < 0.01), respectively. POMC promoter activity, assayed by a -706/+64 rat POMC promoter-luciferase construct, was stimulated by 0.5 x 10(-9) M IL-11 (1.9 +/- 0.06-fold; P < 0.001) and 5 mM Bu2cAMP (7.1 +/- 0.52-fold, P < 0.001), and combined treatment of IL-11 plus Bu2cAMP caused a synergistic 11.7+/-0.71-fold increase ofluciferase activity (P < 0.001 vs. Bu2cAMP alone). Gene expression of SOCS-3, an intracellular inhibitor of cytokine action, peaked as early as 60 min after incubation with IL-11 (0.5 x 10(-9) M) and was induced 3.5-fold. In comparison to mock-transfected AtT-20 cells (AtT-20M), stable overexpression of SOCS-3 (AtT-20S) resulted in significant inhibition of ACTH secretion induced by IL-11 alone (1.5 +/- 0.09 vs. 1.1 +/- 0.04-fold induction, P < 0.01) and IL-11 plus Bu2cAMP (2.1 +/- 0.21 vs. 1.5 +/- 0.06-fold, P < 0.05), but not by Bu2cAMP alone (1.5 +/- 0.12 vs. 1.4 +/- 0.06). In summary, human and murine pituitary express IL-11 and IL-11R transcripts. In murine corticotroph AtT-20 cells, IL- 11 induces POMC gene transcription and ACTH secretion. IL-11 induction of SOCS-3 indicates an intracellular negative feedback control of cytokine-induced POMC expression and ACTH secretion. Thus, IL-11 regulates the HPA axis similarly to LIF, providing further evidence for a redundant cytokine network in the neuro-immuno-endocrine regulation of the HPA axis.

摘要

我们最近将白血病抑制因子(LIF)鉴定为下丘脑 - 垂体 - 肾上腺(HPA)轴活动的重要调节因子。我们现在描述白细胞介素(IL)-11(IL - 6细胞因子家族的另一个成员)在HPA轴的神经 - 免疫 - 内分泌调节中的作用。在小鼠下丘脑、垂体和促肾上腺皮质激素分泌细胞AtT - 20细胞中,仅通过逆转录聚合酶链反应(RT - PCR)可检测到IL - 11信使核糖核酸(mRNA),而通过Northern印迹法证实了IL - 11受体(IL - 11R)mRNA转录本的存在。使用RT - PCR,在正常人垂体以及促肾上腺皮质激素分泌性和无功能性垂体腺瘤中也检测到了IL - 11和IL - 11R基因表达。用10⁻⁹ M IL - 11孵育AtT - 20细胞24小时,刺激促肾上腺皮质激素(ACTH)分泌增加1.4±0.1倍(P < 0.01),而相同浓度的LIF则使ACTH分泌增加1.5±0.1倍(P < 0.001)。阿黑皮素原(POMC)mRNA表达在IL - 11(0.5×10⁻⁹ M)和LIF(0.5×10⁻⁹ M)作用下分别诱导增加1.5±0.18倍(P < 0.05)和1.7±0.13倍(P < 0.01)。通过 - 706 / + 64大鼠POMC启动子 - 荧光素酶构建体检测POMC启动子活性,0.5×10⁻⁹ M IL - 11(1.9±0.06倍;P < 0.001)和5 mM双丁酰环磷腺苷(Bu2cAMP)(7.1±0.52倍,P < 0.001)可刺激其活性,IL - 11与Bu2cAMP联合处理导致荧光素酶活性协同增加11.7±0.71倍(与单独使用Bu2cAMP相比,P < 0.001)。细胞因子作用的细胞内抑制剂细胞因子信号转导抑制因子3(SOCS - 3)的基因表达早在与IL - 11(0.5×10⁻⁹ M)孵育60分钟后达到峰值,并被诱导3.5倍。与mock转染的AtT - 20细胞(AtT - 20M)相比,SOCS - 3的稳定过表达(AtT - 20S)导致单独IL - 11诱导的ACTH分泌显著抑制(诱导倍数分别为1.5±0.09与1.1±0.04倍,P < 0.01)以及IL - 11与Bu2cAMP联合诱导的ACTH分泌显著抑制(诱导倍数分别为2.1±0.21与1.5±0.06倍,P < 0.05),但单独Bu2cAMP诱导的ACTH分泌无显著抑制(诱导倍数分别为1.5±0.12与1.4±0.06)。总之,人和小鼠垂体表达IL - 11和IL - 1lR转录本。在小鼠促肾上腺皮质激素分泌细胞AtT - 20细胞中,IL - 11诱导POMC基因转录和ACTH分泌。IL - 11诱导SOCS - 3表明细胞因子诱导的POMC表达和ACTH分泌存在细胞内负反馈控制。因此,IL - 11与LIF类似地调节HPA轴,为HPA轴的神经 - 免疫 - 内分泌调节中存在冗余细胞因子网络提供了进一步证据。

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