首页> 外文期刊>Surgery >Exogenous ghrelin modulates release of pro-inflammatory and anti-inflammatory cytokines in LPS-stimulated macrophages through distinct signaling pathways.
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Exogenous ghrelin modulates release of pro-inflammatory and anti-inflammatory cytokines in LPS-stimulated macrophages through distinct signaling pathways.

机译:外源性生长素释放肽通过不同的信号传导途径调节LPS刺激的巨噬细胞中促炎和抗炎细胞因子的释放。

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摘要

BACKGROUND: Ghrelin, an orexigenic 28-amino-acid peptide, has been studied primarily in relation to the control of appetite and fat metabolism. In addition to these well-known functions, ghrelin, and its target receptors, growth hormone secretagogue receptors (GHS-Rs), have been localized to neutrophils, lymphocytes, and macrophages, which suggests that ghrelin may be involved in immune modulation. METHODS: To assess the therapeutic role of ghrelin in production of pro-inflammatory and anti-inflammatory cytokines, the effects of exogenous ghrelin administration on the regulation of cytokine release in lipopolysaccharide (LPS)-activated murine RAW 264.7 macrophages were analyzed. RESULTS: Ghrelin and GHS-Rs are expressed in murine macrophages. In addition, exogenous ghrelin inhibited the production of pro-inflammatory cytokines IL-1beta and TNF-alpha in LPS-stimulated murine macrophages in a dose dependent and time-dependent fashion. Exogenous ghrelin pretreatment resulted in a decrease in LPS-induced NFkappaB activation and was presumably the reason for this ghrelin-mediated effect. In contrast to these findings, exogenous ghrelin significantly augmented the release of the anti-inflammatory cytokine IL-10 in a dose-dependent and time-dependent fashion from LPS-stimulated murine macrophages. Ghrelin administration enhanced activation of p38 MAPK, which is known to control the release of IL-10 in macrophages independent of the NFkappaB pathway. These effects of ghrelin on both pro-inflammatory and anti-inflammatory cytokines were offset when a specific GHS-R receptor antagonist was added to the culture media. CONCLUSIONS: These data suggest that ghrelin has potent anti-inflammatory properties through modulation of secretion of both pro-inflammatory and anti-inflammatory cytokines from LPS-stimulated macrophages through distinct signaling cascades. Therapeutic utility of ghrelin to control, modulate, or treat pathologic inflammatory conditions like endotoxemic shock and ulcerative colitis requires additionalinvestigation.
机译:背景:Ghrelin是一种致食性28氨基酸肽,主要研究了食欲和脂肪代谢的控制。除了这些众所周知的功能外,ghrelin及其靶受体,生长激素促分泌素受体(GHS-Rs)已被定位于嗜中性粒细胞,淋巴细胞和巨噬细胞,这表明ghrelin可能参与了免疫调节。方法:为了评估生长素释放肽在促炎和抗炎细胞因子产生中的治疗作用,分析了外源生长素释放肽对脂多糖(LPS)激活的鼠RAW 264.7巨噬细胞中细胞因子释放的调节作用。结果:Ghrelin和GHS-Rs在小鼠巨噬细胞中表达。另外,外源性生长激素释放肽以剂量依赖性和时间依赖性的方式抑制LPS刺激的鼠巨噬细胞中促炎性细胞因子IL-1β和TNF-α的产生。外源性生长激素释放肽预处理导致LPS诱导的NFkappaB激活减少,并且可能是这种生长激素释放肽介导的作用的原因。与这些发现相反,外源性生长素释放肽以剂量依赖性和时间依赖性方式显着增加了LPS刺激的鼠巨噬细胞中抗炎细胞因子IL-10的释放。 Ghrelin给药增强了p38 MAPK的激活,已知该激活可独立于NFkappAB途径控制巨噬细胞中IL-10的释放。当将特定的GHS-R受体拮抗剂添加到培养基中时,ghrelin对促炎和抗炎细胞因子的这些作用被抵消。结论:这些数据表明,生长素释放肽通过调节信号转导途径,从LPS刺激的巨噬细胞分泌促炎和抗炎细胞因子的分泌,具有有效的抗炎特性。生长激素释放肽在控制,调节或治疗诸如内毒素血症性休克和溃疡性结肠炎等病理性炎症中的治疗作用需要进一步的研究。

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