首页> 美国卫生研究院文献>Springer Open Choice >Leptin Activates Human B Cells to Secrete TNF-α IL-6 and IL-10 via JAK2/STAT3 and p38MAPK/ERK1/2 Signaling Pathway
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Leptin Activates Human B Cells to Secrete TNF-α IL-6 and IL-10 via JAK2/STAT3 and p38MAPK/ERK1/2 Signaling Pathway

机译:瘦素激活人类B细胞通过JAK2 / STAT3和p38MAPK / ERK1 / 2信号通路分泌TNF-αIL-6和IL-10

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摘要

Leptin, one of the adipokines, functions as a hormone and a cytokine. In this investigation, we show for the first time that leptin, in a concentration-dependent manner, activates human peripheral blood B cells to induce secretion of IL-6, IL-10, and TNF-α. Leptin increased B cells expressing CD25 and HLA-DR. Leptin induces phosphorylation of Janus activation kinase 2 (JAK2), signal transducer and activator of transcription 3 (STAT3), p38 mitogen-activated protein kinase (p38MAPK), and extracellular signal-regulated kinase (ERK1/2). Furthermore, leptin-induced cytokine secretion by B cells was blocked by inhibitors of JAK2, STAT3, p38MAPK, and ERK1/2. These data demonstrate that leptin activates human B cells to secrete cytokines via activation of JAK2/STAT3 and p38MAPK/ERK1/2 signaling pathways, which may contribute to its inflammatory and immunoregulatory properties.
机译:瘦素是脂肪因子之一,起着激素和细胞因子的作用。在这项研究中,我们首次显示出瘦素以浓度依赖性的方式激活人外周血B细胞以诱导IL-6,IL-10和TNF-α的分泌。瘦素增加表达CD25和HLA-DR的B细胞。瘦素诱导Janus激活激酶2(JAK2),信号转导和转录激活因子3(STAT3),p38丝裂原活化蛋白激酶(p38MAPK)和细胞外信号调节激酶(ERK1 / 2)磷酸化。此外,JAK2,STAT3,p38MAPK和ERK1 / 2抑制剂可阻断B细胞瘦素诱导的细胞因子分泌。这些数据表明瘦素通过激活JAK2 / STAT3和p38MAPK / ERK1 / 2信号通路激活人类B细胞分泌细胞因子,这可能有助于其炎症和免疫调节特性。

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