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哮喘气道重塑中纤维化的调节。

The regulation of fibrosis in airway remodeling in asthma.

机构信息

Department of Allergy and Immunology, Murdoch Children's Research Institute, The Royal Children's Hospital, Melbourne 3052, Australia.

出版信息

Mol Cell Endocrinol. 2012 Apr 4;351(2):167-75. doi: 10.1016/j.mce.2012.01.007. Epub 2012 Jan 14.

Abstract

Fibrosis is one of the key pathological features of airway remodeling in asthma. In the normal airway the amount of collagen and other extracellular matrix components is kept in equilibrium by regulation of synthesis and degradation. In asthma this homeostasis is disrupted due to genetic and environmental factors. In the airways of patients with the disease there is increased extracellular matrix deposition, particularly in the reticular basement membrane region, lamina propria and submucosa. Fibrosis is important as it can occur early in the pathogenesis of asthma, be associated with severity and resistant to therapy. In this review we will discuss current knowledge of relaxin and other key regulators of fibrosis in the airway including TGFβ, Smad2/3 and matrix metalloproteinases. As fibrosis is not directly targeted or effectively treated by current asthma drugs including corticosteroids, characterization of airway fibrosis and how it is regulated will be essential for the development of novel therapies for asthma.

摘要

纤维化是哮喘气道重塑的关键病理特征之一。在正常气道中,胶原和其他细胞外基质成分的量通过合成和降解的调节保持平衡。在哮喘中,由于遗传和环境因素,这种内稳态被打破。在疾病患者的气道中,细胞外基质的沉积增加,特别是在网状基底膜区域、固有层和黏膜下层。纤维化很重要,因为它可能在哮喘的发病早期发生,与严重程度相关,并且对治疗有抗性。在这篇综述中,我们将讨论松弛素和其他关键的气道纤维化调节剂,包括 TGFβ、Smad2/3 和基质金属蛋白酶的最新知识。由于纤维化不是当前哮喘药物(包括皮质类固醇)的直接靶点或有效治疗靶点,因此气道纤维化的特征及其调节方式对于开发哮喘的新疗法至关重要。

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