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首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Airways exudation of plasma macromolecules: Innate defense, epithelial regeneration, and asthma
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Airways exudation of plasma macromolecules: Innate defense, epithelial regeneration, and asthma

机译:气道渗出等离子体大分子:先天防御,上皮再生和哮喘

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This review discusses in vivo airway aspects of plasma exudation in relation to current views on epithelial permeability and epithelial regeneration in health and disease. Microvascular-epithelial exudation of bulk plasma proteins characteristically occurs in asthmatic patients, being especially pronounced in those with severe and exacerbating asthma. Healthy human and guinea pig airways challenged by noninjurious histamine-leukotriene-type autacoids also respond through prompt mucosal exudation of nonsieved plasma macromolecules. Contrary to current beliefs, epithelial permeability in the opposite direction (ie, absorption of inhaled molecules) has not been increased in patients with asthma and allergic rhinitis or in acutely exuding healthy airways. A slightly increased subepithelial hydrostatic pressure produces such unidirectional outward perviousness to macromolecules. Lack of increased absorption permeability in asthmatic patients can further be reconciled with occurrence of epithelial shedding, leaving small patches of denuded basement membrane. Counteracting escalating barrier breaks, plasma exudation promptly covers the denuded patches. Here it creates and sustains a biologically active barrier involving a neutrophil-rich, fibrin-fibronectin net. Furthermore, in the plasma-derived milieu, all epithelial cell types bordering the denuded patch dedifferentiate and migrate from all sides to cover the denuded basement membrane. However, this speedy epithelial regeneration can come at a cost. Guinea pig in vivo studies demonstrate that patches of epithelial denudation regeneration are exudation hot spots evoking asthma-like features, including recruitment/activation of granulocytes, proliferation of fibrocytes/smooth muscle cells, and basement membrane thickening. In conclusion, nonsieved plasma macromolecules can operate on the intact airway mucosa as potent components of first-line innate immunity responses. Exuded plasma also takes center stage in epithelial regeneration. When exaggerated, epithelial regeneration can contribute to the inception and development of asthma.
机译:本综述讨论了血浆渗出的体内呼吸道方面,与目前对健康疾病的上皮渗透性和上皮再生的目前的看法。体血管蛋白的微血管上皮渗出特征在哮喘患者中,在严重和加剧哮喘的那些中特别明显。由非富集组胺 - 白酮型自身自身挑战的健康人和几内亚猪气道也通过迅速的粘膜渗出来响应作用的血浆大分子。与当前的信仰相反,患有哮喘和过敏性鼻炎或急性渗出健康气道的患者患有相反方向(即吸入分子的吸收)的上皮渗透性。略微增加的耻骨静压压力为大分子产生这种单向向外透过的。在哮喘患者中缺乏增加的吸收渗透性可以进一步与上皮脱落的发生,留下小的裸露的地下膜膜。抵消升级的屏障突破,等离子体渗出迅速覆盖裸露的斑块。在这里,它会产生和维持涉及富含中性粒细胞的纤维蛋白 - 纤维蛋白蛋白网的生物学活性屏障。此外,在等离子体衍生的Milieu中,所有上皮细胞类型与裸露的贴片边界过滤和迁移到所有侧面以覆盖裸露的基底膜。然而,这种速度的上皮再生可以成本。豚鼠体内研究表明,上皮剥削再生的斑块是渗出哮喘的特征的渗出热点,包括粒细胞的募集/活化,纤维细胞/平滑肌细胞的增殖,以及基底膜增稠。总之,作理血浆大分子可以在完整的气道粘膜上运行,作为一线先天免疫反应的有效组分。渗出的血浆也占据上皮再生中的中心阶段。夸张时,上皮再生可以有助于哮喘的初始和发展。

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