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IL-10 modulates serotonin transporter activity and molecular expression in intestinal epithelial cells

机译:IL-10调节肠上皮细胞中血清素转运蛋白的活性和分子表达

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摘要

Serotonin is a neuromodulator mainly synthesized by intestinal enterochromaffin cells that regulate overall intestinal physiology. The serotonin transporter (SERT) determines the final serotonin availability and has been described as altered in inflammatory bowel diseases. IL-10 is an anti-inflammatory cytokine that is involved in intestinal inflammatory processes and also contributes to intestinal mucosa homeostasis. The regulation of SERT by pro-inflammatory factors is well known; however, the effect of IL-10 on the intestinal serotoninergic system mediated by SERT remains unknown. Therefore, the aim of the present study is to determine whether IL-10 affects SERT activity and expression in enterocyte-like Caco-2 cells. Treatment with IL-10 was assessed and SERT activity was determined by 5-HT uptake. SERT mRNA and protein expression was analyzed using quantitative RT-PCR and western blotting. The results showed that IL-10 induced a dual effect on SERT after 6. h of treatment. On one hand, IL-10, at a low concentration, inhibited SERT activity, and this effect might be explained by a non-competitive inhibition of SERT. On the other hand, IL-10, at a high concentration, increased SERT activity and molecular expression in the membrane of the cells. This effect was mediated by the IL-10 receptor and triggered by the PI3K intracellular pathway. Our results demonstrate that IL-10 modulates SERT activity and expression, depending on its extracellular conditions. This study may contribute to understand serotoninergic responses in intestinal pathophysiology. ? 2013 Elsevier Ltd.
机译:5-羟色胺是一种神经调节剂,主要由调节整个肠道生理的肠肠嗜铬细胞合成。血清素转运蛋白(SERT)决定了最终的血清素可用性,并已被描述为炎症性肠病的改变。 IL-10是一种抗炎性细胞因子,与肠道炎症过程有关,也有助于肠黏膜体内稳态。促炎因子对SERT的调节是众所周知的。然而,IL-10对由SERT介导的肠道5-羟色胺能系统的影响尚不清楚。因此,本研究的目的是确定IL-10是否影响SERT活性和肠细胞样Caco-2细胞中的表达。评估用IL-10治疗,并通过5-HT摄取确定SERT活性。使用定量RT-PCR和western印迹分析了SERT mRNA和蛋白表达。结果显示IL-10在治疗6小时后对SERT具有双重​​作用。一方面,低浓度的IL-10抑制了SERT活性,这种作用可能是通过非竞争性抑制SERT来解释的。另一方面,高浓度的IL-10可提高SERT活性和细胞膜分子表达。该作用由IL-10受体介导,并由PI3K细胞内途径触发。我们的结果表明,IL-10可以根据其细胞外条件调节SERT活性和表达。这项研究可能有助于了解肠道病理生理学中的5-羟色胺能反应。 ? 2013爱思唯尔有限公司

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