Aubert J D, Dalal B I, Bai T R, Roberts C R, Hayashi S, Hogg J C
UBC Pulmonary Research Laboratory, St Paul's Hospital, Vancouver, British Columbia, Canada.
Thorax. 1994 Mar;49(3):225-32. doi: 10.1136/thx.49.3.225.
Asthmatic airways have a characteristic deposition of connective tissue under the epithelial basement membrane, but the mediators involved in this alteration are unknown. Several authors have postulated that transforming growth factor beta 1 (TGF-beta 1) could be overexpressed in asthmatic airways.
Lung samples from 16 asthmatic patients, six patients with chronic obstructive pulmonary disease (COPD), and six non-obstructed smokers were analysed. RNA was extracted from these tissues to measure expression of TGF-beta 1 by Northern blot analysis using a cDNA probe for TGF-beta 1. The level of expression was quantitated by densitometry using glyceraldehyde 3-phosphate dehydrogenase mRNA as a control. TGF-beta 1 was localised to specific cell types in these lungs by immunohistochemical analysis using polyclonal antibodies specific for intracellular and extracellular TGF-beta 1.
The 2.5 kb TGF-beta 1 mRNA was seen in all 18 samples analysed by Northern blotting and densitometric analysis showed no difference between the asthmatic group (mean (SD) 108% (43%)), the group with COPD (122% (33%)), and the non-obstructed group (100% (49%)). The TGF-beta 1 precursor was immunolocalised throughout the airway wall including the epithelium and in alveolar macrophages. The mature TGF-beta 1 was localised primarily within the connective tissue of the airway wall. These patterns of expression of both forms of TGF-beta 1 were similar in lungs from asthmatic patients, those with COPD, and controls.
While TGF-beta 1 mRNA and protein are abundantly expressed in human lungs, there is no clear difference in expression between the airways of asthmatic subjects and those of smokers with and without COPD.
哮喘气道上皮基底膜下有结缔组织特征性沉积,但参与这种改变的介质尚不清楚。几位作者推测转化生长因子β1(TGF-β1)可能在哮喘气道中过度表达。
分析了16例哮喘患者、6例慢性阻塞性肺疾病(COPD)患者和6例无阻塞性吸烟者的肺样本。从这些组织中提取RNA,使用TGF-β1的cDNA探针通过Northern印迹分析测量TGF-β1的表达。以甘油醛-3-磷酸脱氢酶mRNA作为对照,通过密度测定法定量表达水平。使用针对细胞内和细胞外TGF-β1的多克隆抗体,通过免疫组织化学分析将TGF-β1定位于这些肺中的特定细胞类型。
通过Northern印迹分析的所有18个样本中均可见2.5 kb的TGF-β1 mRNA,密度测定分析显示哮喘组(平均(标准差)108%(43%))、COPD组(122%(33%))和无阻塞组(100%(49%))之间无差异。TGF-β1前体免疫定位于整个气道壁,包括上皮和肺泡巨噬细胞。成熟的TGF-β1主要定位于气道壁的结缔组织内。哮喘患者、COPD患者和对照组肺中两种形式的TGF-β1的这些表达模式相似。
虽然TGF-β1 mRNA和蛋白在人肺中大量表达,但哮喘患者气道与有或无COPD的吸烟者气道之间的表达无明显差异。