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Correlation of hyaluronan deposition with infiltration of eosinophils and lymphocytes in a cockroach-induced murine model of asthma

机译:蟑螂诱发的哮喘小鼠模型中透明质酸沉积与嗜酸性粒细胞和淋巴细胞浸润的相关性

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摘要

Asthma is a chronic inflammatory disease that exhibits airway remodeling with changes in the extracellular matrix (ECM). The role of the ECM in mediating these changes is poorly understood. Hyaluronan (HA), a major component of the ECM, has been implicated in many biological processes in diseases. This study investigates the processes involved in HA synthesis, deposition and localization during the propagation of cockroach-induced asthma. Mice were sensitized and challenged with cockroach antigen, and sacrificed at various time points during an 8-week challenge protocol. Analysis of bronchoalveolar lavage (BAL) fluid revealed an increase in total nucleated cells as early as 6 h, which peaked at 6 days. Histopathologic analysis of the lung tissue revealed an influx of inflammatory cells at the peribronchial and perivascular regions starting at 12 h, which peaked at 6 days and persisted to 8 weeks. Eosinophils predominated in the early time points while lymphocytes predominated during the late time points. Quantitative polymerase chain reaction (PCR) data showed that hyaluronan synthase 1 (HAS1) mRNA peaked within 6 h and then declined. HAS2 mRNA also peaked within 6 h but remained elevated throughout the 8-week exposure course. HA levels in lung tissue and BAL increased at 12 h and peaked by 6 and 8 days, respectively. Inflammatory cells and new collagen formation localized in areas of HA deposition. Taken together, these data support a role for HA in the pathogenesis in asthma.
机译:哮喘是一种慢性炎性疾病,表现为气道重塑,细胞外基质(ECM)发生变化。人们对ECM在调解这些变化中的作用知之甚少。透明质酸(HA)是ECM的主要组成部分,与疾病的许多生物学过程有关。这项研究调查了蟑螂诱发的哮喘传播过程中HA合成,沉积和定位的过程。用蟑螂抗原致敏并攻击小鼠,并在8周的攻击方案中的各个时间点处死小鼠。对支气管肺泡灌洗液(BAL)的分析显示,早在6小时时总有核细胞就增加了,在6天达到峰值。肺组织的组织病理学分析显示,从12小时开始,支气管周围和血管周围区域的炎症细胞大量涌入,在6天达到高峰,并持续8周。嗜酸性粒细胞在早期的时间点占主导地位,而淋巴细胞在晚期的时间点占主导地位。定量聚合酶链反应(PCR)数据显示,透明质酸合酶1(HAS1)mRNA在6小时内达到峰值,然后下降。 HAS2 mRNA也在6小时内达到峰值,但在整个8周的暴露过程中仍保持升高。肺组织中的HA水平和BAL在12小时时升高,分别在6天和8天达到峰值。炎症细胞和新胶原蛋白的形成位于HA沉积区域。综上所述,这些数据支持HA在哮喘发病机理中的作用。

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