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Interleukin-10 attenuates TNF-alpha-induced interleukin-6 production in endometriotic stromal cells.

机译:白细胞介素10减弱子宫内膜异位基质细胞中TNF-α诱导的白细胞介素6的产生。

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OBJECTIVE: To determine whether high levels of interleukin (IL)-10 can attenuate the production of tumor necrosis factor (TNF)-alpha-induced proinflammatory cytokines in endometriotic stromal cells. DESIGN: Prospective study. SETTING: Department of Ob/Gyn, Tottori University, Japan. PATIENT(S): Thirty-five patients with ovarian endometrioma and ten patients with uterine myoma. INTERVENTION(S): Endometriotic stromal cells were obtained from chocolate cyst linings of ovaries. Endometrial stromal cells obtained from patient with uterine myoma. MAIN OUTCOME MEASURE(S): Expression of IL-10 gene in endometriotic or endometrial stromal cells was determined by real-time reverse-transcriptase polymerase chain reaction (RT-PCR). We performed immunohistochemical staining to find the presence of IL-10 and IL-10 receptors 1 and 2. We examined the effects of TNF-alpha and IL-10 on the expression of IL-6 or IL-8 by real-time RT-PCR and ELISA. We examined the activation of intracellular signal transduction molecules in endometriotic stromal cells by Western blotting. RESULT(S): Addition of IL-10 suppressed the expressions of IL-6 induced by TNF-alpha and IL-10 induced the phosphorylation of STAT3 in endometriotic stromal cells. TNF-alpha induced the expression of phosphorylated ERK1/2, JNK1/2, and I kappaB. Adding IL-10 suppressed the phosphorylation of these signal molecules. CONCLUSION(S): Interleukin-10 attenuates TNF-alpha-induced IL-6 synthesis via NF-kappaB and MAPK pathways in endometriotic cells.. Interleukin-10 may play a significant role in the pathogenesis of endometriosis.
机译:目的:确定高水平的白介素(IL)-10是否可以减弱子宫内膜异位基质细胞中肿瘤坏死因子(TNF)-α诱导的促炎细胞因子的产生。设计:前瞻性研究。地点:日本鸟取大学妇产科。患者:35例子宫内膜瘤患者和10例子宫肌瘤患者。干预:子宫内膜异位基质细胞获自卵巢巧克力囊肿衬里。从子宫肌瘤患者获得的子宫内膜基质细胞。主要观察指标:通过实时逆转录酶聚合酶链反应(RT-PCR)确定子宫内膜异位或子宫内膜间质细胞中IL-10基因的表达。我们进行了免疫组织化学染色以发现IL-10和IL-10受体1和2的存在。我们通过实时RT-RT检查了TNF-alpha和IL-10对IL-6或IL-8表达的影响。 PCR和ELISA。我们通过蛋白质印迹检查了子宫内膜异位基质细胞中细胞内信号转导分子的激活。结果:添加IL-10可抑制子宫内膜异位基质细胞中TNF-α诱导的IL-6表达,IL-10诱导STAT3磷酸化。 TNF-α诱导磷酸化ERK1 / 2,JNK1 / 2和I kappaB的表达。加入IL-10抑制了这些信号分子的磷酸化。结论:白细胞介素10通过子宫内膜异位细胞中的NF-κB和MAPK途径减弱了TNF-α诱导的IL-6合成。白细胞介素10可能在子宫内膜异位症的发病机制中起重要作用。

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