Surfactant Proteins in Smoking-Related Lung Disease

被引:14
作者
Papaioannou, Andriana I. [1 ]
Papiris, Spyridon [1 ]
Papadaki, Georgia [1 ]
Manali, Effrosyni D. [1 ]
Roussou, Aneza [1 ]
Spathis, Aris [2 ]
Karakitsos, Petros [2 ]
Kostikas, Konstantinos [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Athens Med Sch, Attikon Univ Hosp, Resp Med Dept 2, Athens, Greece
[2] Natl & Kapodistrian Univ Athens, Athens Med Sch, Attikon Univ Hosp, Dept Cytopathol, Athens 11528, Greece
关键词
Pulmonary Surfactant; Surfactant Proteins; Chronic Obstructive Pulmonary Disease; Idiopathic Pulmonary Fibrosis; Combined Pulmonary Fibrosis and Emphysema; IDIOPATHIC PULMONARY-FIBROSIS; INTERSTITIAL PNEUMONIA; RESPIRATORY-DISEASE; SERUM; EMPHYSEMA; MUTATIONS; BIOMARKERS; COPD; SUSCEPTIBILITY; DEFICIENCY;
D O I
10.2174/1568026616666150930120640
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pulmonary surfactant is a highly surface-active mixture of proteins and lipids that is synthesized and secreted in the alveoli by type II epithelial cells and is found in the fluid lining the alveolar surface. The protein part of surfactant constitutes two hydrophilic proteins (SP-A and SP-D) that regulate surfactant metabolism and have immunologic functions, and two hydrophobic proteins (SP-B and SP-C), which play a direct role in the organization of the surfactant structure in the interphase and in the stabilization of the lipid layers during the respiratory cycle. Several studies have shown that cigarette smoke seems to affect, in several ways, both surfactant homeostasis and function. The alterations in surfactants' biophysical properties caused by cigarette smoking, contribute to the development of several smoking related lung diseases. In this review we provide information on biochemical and physiological aspects of the pulmonary surfactant and on its possible association with the development of two major chronic diseases of the lung known to be related to smoking, i.e. chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF). Additional information on the possible role of surfactant protein alterations and/or dysfunction in the combination of these two conditions, recently described as combined pulmonary fibrosis and emphysema (CPFE) are also provided.
引用
收藏
页码:1574 / 1581
页数:8
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