Alveolar epithelial transport in the adult lung

被引:46
作者
Dobbs, Leland G. [1 ,2 ,3 ]
Johnson, Meshell D. [1 ]
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[2] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Cardiovasc Res Inst, San Francisco, CA 94143 USA
关键词
alveolar liquid regulation; alveolar epithelium; type I cells; type II cells; ion transport; fluid transport; ENaC; ion channels;
D O I
10.1016/j.resp.2007.06.011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The alveolar surface comprises >99% of the internal surface area of the lungs. At birth, the fetal lung rapidly converts from a state of net fluid secretion, which is necessary for normal fetal lung development, to a state in which there is a minimal amount of alveolar liquid. The alveolar surface epithelium facing the air compartment is composed of TI and TII cells. The morphometric characteristics of both cell types are fairly constant over a range of mammalian species varying in body weight by a factor of similar to 50,000. From the conservation of size and shape across species, one may infer that both TI and TII cells also have important conserved functions. The regulation of alveolar ion and liquid transport has been extensively investigated using a variety of experimental models, including whole animal, isolated lung, isolated cell, and cultured cell model systems, each with their inherent strengths and weaknesses. The results obtained with different model systems and a variety of different species point to both interesting parallels and some surprising differences. Sometimes it has been difficult to reconcile results obtained with different model systems. In this section, the primary focus will be on aspects of alveolar ion and liquid transport under normal physiologic conditions, emphasizing newer data and describing evolving paradigms of lung ion and fluid transport. We will highlight some of the unanswered questions, outline the similarities and differences in results obtained with different model systems, and describe some of the complex and interweaving regulatory networks. (C) 2007 Published by Elsevier B.V.
引用
收藏
页码:283 / 300
页数:18
相关论文
共 186 条
[101]   EXPRESSION CLONING OF AN EPITHELIAL AMILORIDE-SENSITIVE NA+ CHANNEL - A NEW CHANNEL TYPE WITH HOMOLOGIES TO CAENORHABDITIS-ELEGANS DEGENERINS [J].
LINGUEGLIA, E ;
VOILLEY, N ;
WALDMANN, R ;
LAZDUNSKI, M ;
BARBRY, P .
FEBS LETTERS, 1993, 318 (01) :95-99
[102]  
LINGUEGLIA E, 1994, J BIOL CHEM, V269, P13736
[103]   Lung fluid transport in aquaporin-5 knockout mice [J].
Ma, TH ;
Fukuda, N ;
Song, YL ;
Matthay, MA ;
Verkman, AS .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (01) :93-100
[104]  
MASON RJ, 1977, FED PROC, V36, P2697
[105]   Maintenance of surfactant protein A and D secretion by rat alveolar type II cells in vitro [J].
Mason, RJ ;
Lewis, MC ;
Edeen, KE ;
McCormick-Shannon, K ;
Nielsen, LD ;
Shannon, JM .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2002, 282 (02) :L249-L258
[106]   TRANS-EPITHELIAL TRANSPORT BY PULMONARY ALVEOLAR TYPE-II CELLS IN PRIMARY CULTURE [J].
MASON, RJ ;
WILLIAMS, MC ;
WIDDICOMBE, JH ;
SANDERS, MJ ;
MISFELDT, DS ;
BERRY, LC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (19) :6033-6037
[107]   PHOSPHOLIPID-COMPOSITION AND ULTRASTRUCTURE OF A549 CELLS AND OTHER CULTURED PULMONARY EPITHELIAL-CELLS OF PRESUMED TYPE-II CELL ORIGIN [J].
MASON, RJ ;
WILLIAMS, MC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1980, 617 (01) :36-50
[108]  
MASON RJ, 1980, J BIOL CHEM, V255, P5101
[109]   Lung edema clearance: 20 years of progress - Invited review: Biophysical properties of sodium channels in lung alveolar epithelial cells [J].
Matalon, S ;
Lazrak, A ;
Jain, L ;
Eaton, DC .
JOURNAL OF APPLIED PHYSIOLOGY, 2002, 93 (05) :1852-1859
[110]   Sodium channels in alveolar epithelial cells: Molecular characterization, biophysical properties, and physiological significance [J].
Matalon, S ;
O'Brodovich, H .
ANNUAL REVIEW OF PHYSIOLOGY, 1999, 61 :627-661