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IL-4Rα-responsive smooth muscle cells contribute to initiation of TH2 immunity and pulmonary pathology in Nippostrongylus brasiliensis infections

机译:IL-4Rα-响应性平滑肌细胞有助于在Nippostrongylus Brasiliensis感染中引发Th2抗扰度和肺病理学

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摘要

Nippostrongylus brasiliensis infections generate pulmonary pathologies that can be associated with strong TH2 polarization of the host's immune response. We present data demonstrating N. brasiliensis-driven airway mucus production to be dependent on smooth muscle cell interleukin 4 receptor-α (IL-4Rα) responsiveness. At days 7 and 10 post infection (PI), significant airway mucus production was found in IL-4Rα−/lox control mice, whereas global knockout (IL-4Rα−/−) and smooth muscle-specific IL-4Rα-deficient mice (SM-MHCCre IL-4Rα−/lox) showed reduced airway mucus responses. Furthermore, interleukin (IL)-13 and IL-5 cytokine production in SM-MHCCre IL-4Rα−/lox mice was impaired along with a transient reduction in T-cell numbers in the lung. In vitro treatment of smooth muscle cells with secreted N. brasiliensis excretory–secretory antigen (NES) induced IL-6 production. Decreased protein kinase C (PKC)-dependent smooth muscle cell proliferation associated with cell cycle arrest was found in cells stimulated with NES. Together, these data demonstrate that both IL-4Rα and NES-driven responses by smooth muscle cells make important contributions in initiating TH2 responses against N. brasiliensis infections.
机译:Nippostrongylus Brasiliensis感染产生肺病理学,可以与宿主免疫应答的强Th2极化相关。我们呈现证明N.Bariliensis驱动的气道粘液生产的数据依赖于平滑肌细胞白细胞介素4受体-α(IL-4Rα)反应性。在第7天和第10天感染后(PI),在IL-4Rα-/ LOX对照小鼠中发现了大量的气道粘液产量,而全球敲除(IL-4Rα - / - )和平滑肌特异性IL-4Rα缺陷小鼠( SM-MHCCRE IL-4Rα-/ LOX)显示出减少的气道粘液反应。此外,SM-MHCCRE IL-4Rα-/ LOX小鼠中的白细胞介素(IL)-13和IL-5细胞因子产生随着肺中T细胞数的瞬态降低。体外处理平滑肌细胞与分泌的N.Bariliensis排泄分泌抗原(NES)诱导IL-6产生。在用NES刺激的细胞中发现了与细胞周期停留相关的蛋白激酶C(PKC)依赖性平滑肌细胞增殖。这些数据一起表明,通过平滑肌细胞的IL-4Rα和NES驱动的反应在启动抗N.Bariliensis感染的响应中作出了重要贡献。

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