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β-肾上腺素能刺激小鼠棕色脂肪细胞中白细胞介素-1α和白细胞介素-6的表达。

beta-Adrenergic stimulation of interleukin-1alpha and interleukin-6 expression in mouse brown adipocytes.

作者信息

Burýsek L, Houstek J

机构信息

Institute of Physiology, Academy of Sciences of the Czech Republic, Prague.

出版信息

FEBS Lett. 1997 Jul 7;411(1):83-6. doi: 10.1016/s0014-5793(97)00671-6.

Abstract

Mouse brown adipocytes in primary culture were shown to contain high levels of mRNA for interleukin-1alpha (IL-1alpha) which could be further stimulated up to 9-fold by norepinephrine (NE). Even higher stimulation by NE, up to 40-fold, was found in case of interleukin-6 (IL-6). Time-course of activation of both genes was biphasic, but the response of IL-6 gene was slower than of IL-1alpha gene. IL-1alpha mRNA level reached the maximum after 1 h and the second, lower increase, occurred after 8 h. IL-6 mRNA level showed first maximum after 2 h, but the highest level was found after 8 h. Similarly to NE, the expression of IL-1alpha and IL-6 genes was stimulated by selective beta-adrenergic agonist isoproterenol, beta3-selective agonist CGP-12117, forskoline and db-cAMP. The activation of both genes by CGP-12177 was dose-dependent with the optimum at 100 nM concentration. Stimulation of alpha-adrenergic receptors by cirazoline and oxymetazoline was without any effect. When the expression of IL-6 was studied at the protein level, the stimulation of IL-6 gene via beta3-receptors resulted in secretion of IL-6 up to the concentration 10 ng/ml culture media in 24 h. The results indicate a new type of regulation of expression of IL-1alpha and IL-6 genes in brown adipocytes by catecholamines acting via beta3-adrenergic receptors. The resulting increase in IL-6 production by brown adipocytes could significantly contribute to systemic levels of IL-6.

摘要

原代培养的小鼠棕色脂肪细胞被证明含有高水平的白细胞介素-1α(IL-1α)mRNA,去甲肾上腺素(NE)可将其进一步刺激高达9倍。在白细胞介素-6(IL-6)的情况下,发现NE的刺激作用甚至更高,可达40倍。两个基因的激活时间进程都是双相的,但IL-6基因的反应比IL-1α基因慢。IL-1αmRNA水平在1小时后达到最大值,第二次较低的增加出现在8小时后。IL-6mRNA水平在2小时后首次达到最大值,但在8小时后发现最高水平。与NE类似,IL-1α和IL-6基因的表达受到选择性β-肾上腺素能激动剂异丙肾上腺素、β3选择性激动剂CGP-12117、福斯高林和二丁酰环磷腺苷(db-cAMP)的刺激。CGP-12177对两个基因的激活呈剂量依赖性,最佳浓度为100 nM。可乐定和羟甲唑啉对α-肾上腺素能受体的刺激没有任何作用。当在蛋白质水平研究IL-6的表达时,通过β3受体对IL-6基因的刺激导致在24小时内IL-6分泌到培养基中的浓度高达10 ng/ml。结果表明,儿茶酚胺通过β3肾上腺素能受体对棕色脂肪细胞中IL-1α和IL-6基因的表达进行了一种新型调节。棕色脂肪细胞产生的IL-6增加可能对全身IL-6水平有显著贡献。

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