首页> 美国卫生研究院文献>Mediators of Inflammation >Differential Influence of Inositol Hexaphosphate on the Expression of Genes Encoding TGF-β Isoforms and Their Receptors in Intestinal Epithelial Cells Stimulated with Proinflammatory Agents
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Differential Influence of Inositol Hexaphosphate on the Expression of Genes Encoding TGF-β Isoforms and Their Receptors in Intestinal Epithelial Cells Stimulated with Proinflammatory Agents

机译:六磷酸肌醇对促炎剂刺激的肠上皮细胞中编码TGF-β亚型及其受体的基因的差异影响

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摘要

Transforming growth factor β (TGF-β) is a multifunctional cytokine recognized as an important regulator of inflammatory responses. The effect of inositol hexaphosphate (IP6), a naturally occurring phytochemical, on the mRNA expression of TGF-β1, TGF-β2, TGF-β3 and TβRI, TβRII, and TβRIII receptors stimulated with bacterial lipopolysaccharides (Escherichia coli and Salmonella typhimurium) and IL-1β in intestinal cells Caco-2 for 3 and 12 h was investigated. Real-time qRT-PCR was used to validate mRNAs level of examined genes. Bacterial endotoxin promoted differential expression of TGF-βs and their receptors in a time-dependent manner. IL-1β upregulated mRNA levels of all TGF-βs and receptors at both 3 h and 12 h. IP6 elicited the opposed to LPS effect by increasing downregulated transcription of the examined genes and suppressing the expression of TGF-β1 at 12 h. IP6 counteracted the stimulatory effect of IL-1β on TGF-β1 and receptors expression by decreasing their mRNA levels. IP6 enhanced LPS- and IL-1β-stimulated mRNA expression of TGF-β2 and -β3. Based on these studies it may be concluded that IP6 present in the intestinal milieu may exert immunoregulatory effects and chemopreventive activity on colonic epithelium under inflammatory conditions or during microbe-induced infection/inflammation by modulating the expression of genes encoding TGF-βs and their receptors at transcriptional level.
机译:转化生长因子β(TGF-β)是一种多功能细胞因子,被认为是炎症反应的重要调节剂。天然肌醇六磷酸肌醇(IP6)对细菌脂多糖刺激的TGF-β1,TGF-β2,TGF-β3和TβRI,TβRII和TβRIII受体mRNA表达的影响研究了肠细胞Caco-2中em>和鼠伤寒沙门氏菌(em>)和IL-1 β 3和12 h。实时qRT-PCR用于验证所检查基因的mRNA水平。细菌内毒素以时间依赖性的方式促进TGF- β s及其受体的差异表达。 IL-1 β 分别在3 andh和12 h上调所有TGF- β s和受体的mRNA水平。 IP6通过增加受检基因的下调转录和抑制TGF- β 1在12 h的表达而引起了与LPS作用相反的作用。 IP6通过降低mRNA的表达来抵消IL-1 β 对TGF- β 1和受体表达的刺激作用水平。 IP6增强了LPS-和IL-1 β 刺激的TGF- β 2和-的mRNA表达> β 3。根据这些研究,可以得出结论,在炎症条件下或在微生物诱导的感染/炎症过程中,肠环境中的IP6可能通过调节TGF- β s及其受体在转录水平上。

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