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大鼠肝脏巨噬细胞释放白细胞介素-6。

Interleukin-6 release by rat liver macrophages.

作者信息

Busam K J, Bauer T M, Bauer J, Gerok W, Decker K

机构信息

Biochemisches Institut, Universität Freiburg, Federal Republic of Germany.

出版信息

J Hepatol. 1990 Nov;11(3):367-73. doi: 10.1016/0168-8278(90)90223-e.

Abstract

Tissue macrophages of the liver (Kupffer cells) release interleukin-6 (IL-6) in vitro. Since Kupffer cells reside in close proximity to hepatocytes, which are major target cells of IL-6, the regulation of IL-6 release by hepatic macrophages has been investigated in this study. Using the hybridoma growth test to detect IL-6, we found that Kupffer cells already maximally release IL-6 at endotoxin concentrations as low as 1.0 ng/ml. The stimulated secretion of IL-6 was increased 4-8-fold by endotoxin when compared to the control macrophages incubated in serum-containing medium alone. The preincubation of macrophages with interferon-gamma enhanced the capacity of Kupffer cells to respond to endotoxin. The secretion of IL-6 could also be induced by interleukin (IL)-1 beta and tumor necrosis factor (TNF-alpha). The most potent inducers, however, were the paramyxoviruses Newcastle Disease Virus and Sendai Virus. The release of IL-6 by macrophages upon stimulation with endotoxin was almost completely inhibited by 1 microM dexamethasone. Whereas 100 nM of prostaglandin E2 (PGE2) inhibited the release of TNF-alpha in rat Kupffer cells, it did not affect the secretion of IL-6.

摘要

肝脏组织巨噬细胞(库普弗细胞)在体外可释放白细胞介素-6(IL-6)。由于库普弗细胞紧邻肝细胞,而肝细胞是IL-6的主要靶细胞,因此本研究对肝脏巨噬细胞释放IL-6的调节进行了研究。利用杂交瘤生长试验检测IL-6,我们发现库普弗细胞在内毒素浓度低至1.0 ng/ml时就已最大程度地释放IL-6。与仅在含血清培养基中孵育的对照巨噬细胞相比,内毒素刺激后IL-6的分泌增加了4至8倍。巨噬细胞与干扰素-γ预孵育可增强库普弗细胞对内毒素的反应能力。白细胞介素(IL)-1β和肿瘤坏死因子(TNF-α)也可诱导IL-6的分泌。然而,最有效的诱导剂是副粘病毒新城疫病毒和仙台病毒。用内毒素刺激巨噬细胞后,1 microM地塞米松几乎完全抑制了IL-6的释放。虽然100 nM前列腺素E2(PGE2)抑制大鼠库普弗细胞中TNF-α的释放,但它不影响IL-6的分泌。

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