TGF-β Signaling Pathways in Different Compartments of the Lower Airways of Patients With Stable COPD

被引:53
作者
Di Stefano, Antonino [1 ,2 ]
Sangiorgi, Claudia [1 ,2 ]
Gnemmi, Isabella [1 ,2 ]
Casolari, Paolo [3 ]
Brun, Paola [5 ]
Ricciardolo, Fabio L. M. [6 ]
Contoli, Marco [3 ]
Papi, Alberto [3 ]
Maniscalco, Pio [4 ]
Ruggeri, Paolo [7 ]
Girbino, Giuseppe [7 ]
Cappello, Francesco [8 ,9 ]
Pavlides, Stelios [10 ,11 ]
Guo, Yike [10 ,11 ]
Chung, Kian Fan [12 ]
Barnes, Peter J. [12 ]
Adcock, Ian M. [12 ,13 ]
Balbi, Bruno [1 ,2 ]
Caramori, Gaetano [3 ,7 ]
机构
[1] IRCCS, Soc Benefit, SpA, Ist Clin Sci Maugeri,Div Pneumol, Veruno, NO, Italy
[2] IRCCS, Soc Benefit, SpA, Ist Clin Sci Maugeri,Lab Citoimmunopatol Apparato, Veruno, NO, Italy
[3] Univ Ferrara, Sez Med Interna & Cardioresp, Ctr Interdipartimentale Studio Malattie Infiammat, Ferrara, Italy
[4] Azienda Osped Univ S Anna, Modulo Chirurg Torac, Ferrara, Italy
[5] Univ Padua, Dipartimento Med Mol, Padua, Italy
[6] Univ Turin, Osped San Luigi, Dipartimento Sci Clin & Biol, AOU, Turin, Italy
[7] Univ Messina, Dipartimento Sci Biomed Odontoiatr & Immagini Mor, Unita Operat Complessa Pneumol, Messina, Italy
[8] Univ Palermo, Sez Anat Umana, Dipartimento Biomed Sperimentale & Neurosci Clin, Palermo, Italy
[9] Euromediterranean Inst Sci & Technol IEMEST, Palermo, Italy
[10] Imperial Coll London, Dept Comp, London, England
[11] Imperial Coll London, Data Sci Inst, London, England
[12] Imperial Coll London, Natl Heart & Lung Inst, Airways Dis Sect, London, England
[13] Hunter Med Res Inst, Prior Res Ctr Lung Hlth, New Lambton Hts, NSW, Australia
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
airway inflammation; autoimmunity; BAMBI; CTGF; SMAD; TGF-beta; OBSTRUCTIVE PULMONARY-DISEASE; GROWTH-FACTOR-BETA; BINDING-PROTEINS; GENE-EXPRESSION; TRANSFORMING GROWTH-FACTOR-BETA-1; CIGARETTE-SMOKE; DOWN-REGULATION; EMPHYSEMA; PATHOGENESIS; ASTHMA;
D O I
10.1016/j.chest.2017.12.017
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: The expression and localization of transforming growth factor-beta (TGF-beta) pathway proteins in different compartments of the lower airways of patients with stable COPD is unclear. We aimed to determine TGF-beta pathway protein expression in patients with stable COPD. METHODS: The expression and localization of TGF-beta pathway components was measured in the bronchial mucosa and peripheral lungs of patients with stable COPD (n = 44), control smokers with normal lung function (n = 24), and control nonsmoking subjects (n = 11) using immunohistochemical analysis. RESULTS: TGF-beta 1, TGF-beta 3, and connective tissue growth factor expression were significantly decreased in the bronchiolar epithelium, with TGF-beta 1 also decreased in alveolar macrophages, in patients with stable COPD compared with control smokers with normal lung function. TGF-beta 3 expression was increased in the bronchial lamina propria of both control smokers with normal lung function and smokers with mild/moderate stable COPD compared with control nonsmokers and correlated significantly with pack-years of smoking. However, TGF-beta 3(+) cells decreased in patients with severe/very severe COPD compared with control smokers. Latent TGF-beta binding protein 1 expression was increased in the bronchial lamina propria in subjects with stable COPD of all severities compared with control smokers with normal lung function. Bone morphogenetic protein and activin membrane-bound inhibitor expression (BAMBI) in the bronchial mucosa was significantly increased in patients with stable COPD of all severities compared with control subjects. No other significant differences were observed between groups for all the other molecules studied in the bronchial mucosa and peripheral lung. CONCLUSIONS: Expression of TGF-beta s and their regulatory proteins is distinct within different lower airway compartments in stable COPD. Selective reduction in TGF-beta 1 and enhanced BAMBI expression may be associated with the increase in autoimmunity in COPD.
引用
收藏
页码:851 / 862
页数:12
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