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Spatio-temporal localization of vasoactive intestinal peptide and neutral endopeptidase in allergic murine lungs

机译:变应性鼠肺中血管活性肠肽和中性内肽酶的时空定位

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摘要

Vasoactive intestinal peptide (VIP) is a neuropeptide with cytokine properties that is abundant in the lung. VIP null mice exhibit spontaneous airway inflammation and hyperresponsiveness emphasizing VIP's "anti-asthma" potential. Although VIP's impending protective role in the lung has been demonstrated, its localization in the naive and allergic murine lungs has not. To this aim, we analyzed the availability of VIP and its protease, neutral peptidase (NEP), in naive and Aspergillus-sensitized and challenged murine lungs after 3, 7, and 14 days. Both VIP and NEP were predominantly localized to the columnar epithelia of the airways in naive lungs. A marked decrease in VIP occurred in these cells 3 days after allergen challenge. NEP localization in the columnar epithelia decreased after allergen challenge. At day 14, VIP localization in the columnar epithelia and arteriolar smooth muscle increased while NEP localization at these sites remained low. This study provides new insights into the local regulation of VIP in the columnar epithelia of the allergic lung. Its altered availability in the context of allergy provides fresh evidence for the modulation of pulmonary inflammation by VIP. (C) 2010 Elsevier B.V. All rights reserved.
机译:血管活性肠肽(VIP)是一种具有细胞因子特性的神经肽,在肺中含量很高。 VIP空小鼠表现出自发性气道炎症和反应过度,强调了VIP的“抗哮喘”潜力。尽管已证明VIP即将在肺中发挥保护作用,但尚未定位在幼稚和过敏性鼠肺中。为此,我们分析了在3天,7天和14天后天真和曲霉菌敏感和攻击的鼠肺中VIP及其蛋白酶,中性肽酶(NEP)的可用性。 VIP和NEP均主要位于幼稚肺中气道的柱状上皮。过敏原攻击后3天,这些细胞的VIP明显减少。变应原攻击后,柱状上皮中的NEP定位降低。在第14天,柱状上皮和小动脉平滑肌的VIP定位增加,而这些部位的NEP定位保持较低。这项研究为过敏性肺柱状上皮中VIP的局部调节提供了新的见解。在变态反应中其可利用性的改变为VIP调节肺部炎症提供了新的证据。 (C)2010 Elsevier B.V.保留所有权利。

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