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针对哮喘气道平滑肌肥大:时机已到的一种方法。

Targeting Airway Smooth Muscle Hypertrophy in Asthma: An Approach Whose Time Has Come.

作者信息

Chetty Anne, Nielsen Heber C

机构信息

Tufts Medical Center, Tufts University, Boston, MA, USA.

出版信息

J Asthma Allergy. 2021 May 25;14:539-556. doi: 10.2147/JAA.S280247. eCollection 2021.

Abstract

Airway smooth muscle (ASM) cell dysfunction is an important component of several obstructive pulmonary diseases, particularly asthma. External stimuli such as allergens, dust, air pollutants, and change in environmental temperatures provoke ASM cell hypertrophy, proliferation, and migration without adequate mechanistic controls. ASM cells can switch between quiescent, migratory, and proliferative phenotypes in response to extracellular matrix proteins, growth factors, and other soluble mediators. While some aspects of airway hypertrophy and remodeling could have beneficial effects, in many cases these contribute to a clinical phenotype of difficult to control asthma. In this review, we discuss the factors responsible for ASM hypertrophy and proliferation in asthma, focusing on cytokines, growth factors, and ion transporters, and discuss existing and potential approaches that specifically target ASM hypertrophy to reduce the ASM mass and improve asthma symptoms. The goal of this review is to highlight strategies that appear ready for translational investigations to improve asthma therapy.

摘要

气道平滑肌(ASM)细胞功能障碍是多种阻塞性肺部疾病(尤其是哮喘)的重要组成部分。过敏原、灰尘、空气污染物和环境温度变化等外部刺激会引发ASM细胞肥大、增殖和迁移,且缺乏适当的机制控制。ASM细胞可根据细胞外基质蛋白、生长因子和其他可溶性介质,在静止、迁移和增殖表型之间转换。虽然气道肥大和重塑的某些方面可能具有有益作用,但在许多情况下,这些会导致难以控制的哮喘临床表型。在本综述中,我们讨论了哮喘中导致ASM肥大和增殖的因素,重点关注细胞因子、生长因子和离子转运体,并讨论了专门针对ASM肥大以减少ASM质量和改善哮喘症状的现有及潜在方法。本综述的目的是突出那些似乎已准备好进行转化研究以改善哮喘治疗的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a78/8164696/71a67ea10085/JAA-14-539-g0001.jpg

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