Fibrogenic Reactions in Lung Disease

被引:92
作者
Araya, Jun [1 ]
Nishimura, Stephen L. [2 ]
机构
[1] Jikei Univ, Sch Med, Div Resp Dis, Dept Internal Med, Tokyo 1058461, Japan
[2] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94110 USA
基金
美国国家卫生研究院;
关键词
airway; asthma; emphysema; interstitial fibrosis; GROWTH-FACTOR-BETA; OBSTRUCTIVE PULMONARY-DISEASE; LATENT TGF-BETA; USUAL INTERSTITIAL PNEUMONIA; EPITHELIAL-MESENCHYMAL TRANSITION; SMALL AIRWAY DIMENSIONS; TRANSFORMING GROWTH-FACTOR-BETA-1; GENE-EXPRESSION; SMOOTH-MUSCLE; MYOFIBROBLAST DIFFERENTIATION;
D O I
10.1146/annurev.pathol.4.110807.092217
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Fibrogenic lung reactions occur as a common phenotype shared among disorders of heterogeneous etiologies. Even with a common etiology, the extent and pattern of fibrosis vary greatly among individuals, even within families, suggesting complex gene-environment interactions. The search for mechanisms shared among all fibrotic lung diseases would represent a major advance in the identification of therapeutic targets that could have a broad impact on lung health. Although it is difficult to grasp all of the complexities of the varied cell types and cytokine networks involved in lung fibrogenic responses, and to predict the biologic responses to the overexpression or deficiency of individual cytokines, a large body of evidence converges on a single common theme: the central importance of the transforming growth factor beta (TGF-beta) pathway. Therapies that act upstream or downstream of TGF-beta activation have the therapeutic potential to treat all fibrogenic responses in the lung.
引用
收藏
页码:77 / 98
页数:22
相关论文
共 132 条
[31]   Telomerase in alveolar epithelial development and repair [J].
Driscoll, B ;
Buckley, S ;
Bui, KC ;
Anderson, KD ;
Warburton, D .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2000, 279 (06) :L1191-L1198
[32]   A COMPARISON OF QUANTITATIVE ANATOMY OF BRONCHI IN NORMAL SUBJECTS IN STATUS ASTHMATICUS IN CHRONIC BRONCHITIS AND IN EMPHYSEMA [J].
DUNNILL, MS ;
MASSARELLA, GR ;
ANDERSON, JA .
THORAX, 1969, 24 (02) :176-+
[33]   DEVELOPMENTALLY REGULATED CONVERSION OF MESENCHYME TO EPITHELIUM [J].
EKBLOM, P .
FASEB JOURNAL, 1989, 3 (10) :2141-2150
[34]   The myofibroblast: phenotypic characterization as a prerequisite to understanding its functions in translational medicine [J].
Eyden, B. .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2008, 12 (01) :22-37
[35]   Fibroblastic foci in usual interstitial pneumonia - Idiopathic versus collagen vascular disease [J].
Flaherty, KR ;
Colby, TV ;
Travis, WD ;
Toews, GB ;
Mumford, J ;
Murray, S ;
Thannickal, VJ ;
Kazerooni, EA ;
Gross, BH ;
Lynch, JP ;
Martinez, FJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 167 (10) :1410-1415
[36]   TGF-β, Smad3 and the process of progressive fibrosis [J].
Gauldie, J. ;
Bonniaud, P. ;
Sime, P. ;
Ask, K. ;
Kolb, M. .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2007, 35 :661-664
[37]   Costimulation of fibroblast collagen and transforming growth factor beta(1) gene expression by monocyte chemoattractant protein-1 via specific receptors [J].
GharaeeKermani, M ;
Denholm, EM ;
Phan, SH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (30) :17779-17784
[38]   Is COPD a rare disease? Prevalence and identification rates in smokers aged 40 years and over within general practice in Germany [J].
Gingter, Christian ;
Wilm, Stefan ;
Abholz, Heinz-Harald .
FAMILY PRACTICE, 2009, 26 (01) :3-9
[39]   EFFECT OF ANTIBODY TO TRANSFORMING GROWTH-FACTOR-BETA ON BLEOMYCIN-INDUCED ACCUMULATION OF LUNG COLLAGEN IN MICE [J].
GIRI, SN ;
HYDE, DM ;
HOLLINGER, MA .
THORAX, 1993, 48 (10) :959-966
[40]  
Halpin David M G, 2006, Proc Am Thorac Soc, V3, P619, DOI 10.1513/pats.200603-093SS