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Histamine utilizes JAK-STAT pathway in regulating cytokine production.

机译:组胺利用JAK-STAT途径调节细胞因子的产生。

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摘要

Histamine shifts TH1/TH2 cytokine balance from TH1 to TH2 cytokines. The phosphorylation of STAT factors and their translocation to nucleus are important steps in the regulation of TH1/TH2 cytokine balance. This study was designed to investigate the effects of histamine on Janus kinases-signal transducers and activators of transcription (JAK-STAT) pathway. The splenocytes were treated with histamine in the presence or absence of JAK-STAT inhibitor, tyrphostin, activated with IFNgamma for 30 min, and phosphorylated STAT1 was detected by immunoblotting. We found that histamine up-regulated the phosphorylation of STATI and tyrphostin prevented this phosphorylation. We then studied the effects of tyrphostin on histamine-mediated inhibition of IFNgamma production and histamine-mediated stimulation of IL-5 and IL-10 production. Tyrphostin dose-dependently reversed the effects of histamine on IFNgamma, IL-5 and IL-10 production, as evident by ELISA. These observations suggest that histamine regulated JAK-STAT signal transduction, which is involved in cytokine secretion.
机译:组胺将TH1 / TH2细胞因子平衡从TH1转移到TH2细胞因子。 STAT因子的磷酸化及其向核的转运是调节TH1 / TH2细胞因子平衡的重要步骤。本研究旨在研究组胺对Janus激酶信号转导子和转录激活子(JAK-STAT)途径的影响。在存在或不存在JAK-STAT抑制剂tyrphostin的情况下,用组胺处理脾细胞,用IFNγ激活30分钟,然后通过免疫印迹检测磷酸化的STAT1。我们发现,组胺上调了STATI的磷酸化,而酪蛋白则阻止了这种磷酸化。然后,我们研究了酪氨酸蛋白酶抑制剂对组胺介导的IFNγ产生抑制作用和组胺介导的IL-5和IL-10产生刺激的作用。如ELISA所示,酪氨酸磷酸酶剂量依赖性地逆转了组胺对IFNγ,IL-5和IL-10产生的影响。这些观察结果表明,组胺调节JAK-STAT信号转导,其参与细胞因子的分泌。

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