Suppr超能文献

哮喘患者与非哮喘患者气道平滑肌细胞介导的凝胶收缩比较。

Comparison of gel contraction mediated by airway smooth muscle cells from patients with and without asthma.

作者信息

Matsumoto Hisako, Moir Lyn M, Oliver Brian G G, Burgess Janette K, Roth Michael, Black Judith L, McParland Brent E

机构信息

Discipline of Pharmacology, University of Sydney, NSW 2006, Australia.

出版信息

Thorax. 2007 Oct;62(10):848-54. doi: 10.1136/thx.2006.070474. Epub 2007 Apr 5.

Abstract

BACKGROUND

Exaggerated bronchial constriction is the most significant and life threatening response of patients with asthma to inhaled stimuli. However, few studies have investigated the contractility of airway smooth muscle (ASM) from these patients. The purpose of this study was to establish a method to measure contraction of ASM cells by embedding them into a collagen gel, and to compare the contraction between subjects with and without asthma.

METHODS

Gel contraction to histamine was examined in floating gels containing cultured ASM cells from subjects with and without asthma following overnight incubation while unattached (method 1) or attached (method 2) to casting plates. Smooth muscle myosin light chain kinase protein levels were also examined.

RESULTS

Collagen gels containing ASM cells reduced in size when stimulated with histamine in a concentration-dependent manner and reached a maximum at a mean (SE) of 15.7 (1.2) min. This gel contraction was decreased by inhibitors for phospholipase C (U73122), myosin light chain kinase (ML-7) and Rho kinase (Y27632). When comparing the two patient groups, the maximal decreased area of gels containing ASM cells from patients with asthma was 19 (2)% (n = 8) using method 1 and 22 (3)% (n = 6) using method 2, both of which were greater than that of cells from patients without asthma: 13 (2)% (n = 9, p = 0.05) and 10 (4)% (n = 5, p = 0.024), respectively. Smooth muscle myosin light chain kinase levels were not different between the two groups.

CONCLUSION

The increased contraction of asthmatic ASM cells may be responsible for exaggerated bronchial constriction in asthma.

摘要

背景

支气管过度收缩是哮喘患者对吸入刺激最显著且危及生命的反应。然而,很少有研究调查这些患者气道平滑肌(ASM)的收缩性。本研究的目的是建立一种通过将ASM细胞嵌入胶原凝胶中来测量其收缩的方法,并比较哮喘患者和非哮喘患者之间的收缩情况。

方法

在过夜孵育后,将来自哮喘患者和非哮喘患者的培养ASM细胞置于漂浮凝胶中,分别采用未附着(方法1)或附着(方法2)于铸型板的方式,检测凝胶对组胺的收缩情况。同时也检测了平滑肌肌球蛋白轻链激酶蛋白水平。

结果

含有ASM细胞的胶原凝胶在组胺刺激下尺寸减小,呈浓度依赖性,平均(标准误)在15.7(1.2)分钟时达到最大收缩。磷脂酶C抑制剂(U73122)、肌球蛋白轻链激酶抑制剂(ML-7)和Rho激酶抑制剂(Y27632)可减少这种凝胶收缩。比较两组患者时,采用方法1,哮喘患者的ASM细胞凝胶最大收缩面积减少19(2)%(n = 8),采用方法2为22(3)%(n = 6),均大于非哮喘患者细胞的收缩面积:分别为13(2)%(n = 9,p = 0.05)和10(4)%(n = 5، p = 0.024)。两组间平滑肌肌球蛋白轻链激酶水平无差异。

结论

哮喘患者ASM细胞收缩增加可能是哮喘患者支气管过度收缩的原因。

相似文献

4
Downregulation of protein phosphatase 2Aα in asthmatic airway smooth muscle.哮喘气道平滑肌中蛋白磷酸酶2Aα的下调
Am J Physiol Lung Cell Mol Physiol. 2024 May 1;326(5):L651-L659. doi: 10.1152/ajplung.00050.2024. Epub 2024 Mar 26.

引用本文的文献

2
Advances in respiratory physiology in mouse models of experimental asthma.实验性哮喘小鼠模型中呼吸生理学的进展。
Front Physiol. 2023 Mar 16;14:1099719. doi: 10.3389/fphys.2023.1099719. eCollection 2023.
4
Airway smooth muscle function in asthma.哮喘中的气道平滑肌功能
Front Physiol. 2022 Oct 5;13:993406. doi: 10.3389/fphys.2022.993406. eCollection 2022.
5
Muscarinic receptor M3 activation promotes fibrocytes contraction.毒蕈碱受体M3激活促进纤维细胞收缩。
Front Pharmacol. 2022 Sep 6;13:939780. doi: 10.3389/fphar.2022.939780. eCollection 2022.

本文引用的文献

2
Transforming growth factor-beta induces airway smooth muscle hypertrophy.转化生长因子-β 诱导气道平滑肌肥大。
Am J Respir Cell Mol Biol. 2006 Feb;34(2):247-54. doi: 10.1165/rcmb.2005-0166OC. Epub 2005 Oct 20.
7
Airway wall remodeling: friend or foe?气道壁重塑:敌还是友?
J Appl Physiol (1985). 2003 Jul;95(1):426-34. doi: 10.1152/japplphysiol.00159.2003.
10
Airway structural alterations selectively associated with severe asthma.气道结构改变与重度哮喘选择性相关。
Am J Respir Crit Care Med. 2003 May 15;167(10):1360-8. doi: 10.1164/rccm.200209-1030OC. Epub 2003 Jan 16.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验