Glucose homeostasis across human airway epithelial cell monolayers: role of diffusion, transport and metabolism

被引:49
作者
Kalsi, Kameljit K. [1 ]
Baker, Emma H. [1 ]
Fraser, Owen [2 ]
Chung, Yuen-Li [1 ]
Mace, Oliver J. [1 ]
Tarelli, Edward [2 ]
Philips, Barbara J. [1 ]
Baines, Deborah L. [1 ]
机构
[1] Univ London, Div Basic Med Sci, Ctr Ion Channel & Cell Signalling, London SW17 0RE, England
[2] Univ London, Biom Ctr, London SW17 0RE, England
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2009年 / 457卷 / 05期
基金
英国惠康基金;
关键词
Glucose; Glucose transport; Epithelium; Airways; Metabolism; ACTIVATED PROTEIN-KINASE; NA+ TRANSPORT; PERMEABILITY; ABSORPTION; HYPERGLYCEMIA; BARRIER; RATS; ION;
D O I
10.1007/s00424-008-0576-4
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Glucose in airway surface liquid (ASL) is maintained at low concentrations compared to blood glucose. Using radiolabelled [H-3]- d-glucose and [C-14]-l-glucose, detection of d- and l-glucose by high-performance liquid chromatography and metabolites by nuclear magnetic resonance, we found that glucose applied to the basolateral side of H441 human airway epithelial cell monolayers at a physiological concentration (5 mM) crossed to the apical side by paracellular diffusion. Transepithelial resistance of the monolayer was inversely correlated with paracellular diffusion. Appearance of glucose in the apical compartment was reduced by uptake of glucose into the cell by basolateral and apical phloretin-sensitive GLUT transporters. Glucose taken up into the cell was metabolised to lactate which was then released, at least in part, across the apical membrane. We suggest that glucose transport through GLUT transporters and its subsequent metabolism in lung epithelial cells help to maintain low glucose concentrations in human ASL which is important for protecting the lung against infection.
引用
收藏
页码:1061 / 1070
页数:10
相关论文
共 42 条
[1]   QUANTITATIVE APPROACHES TO DELINEATE PARACELLULAR DIFFUSION IN CULTURED EPITHELIAL-CELL MONOLAYERS [J].
ADSON, A ;
RAUB, TJ ;
BURTON, PS ;
BARSUHN, CL ;
HILGERS, AR ;
AUDUS, KL ;
HO, NFH .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1994, 83 (11) :1529-1536
[2]   EFFECTS OF PHLORETIN AND DEXTRAN-LINKED PHLORETIN ON PANCREATIC-ISLET METABOLISM AND INSULIN RELEASE [J].
ASHCROFT, SJH ;
NINO, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1978, 538 (02) :334-342
[3]   Hyperglycemia and cystic fibrosis alter respiratory fluid glucose concentrations estimated by breath condensate analysis [J].
Baker, Emma H. ;
Clark, Nicholas ;
Brennan, Amanda L. ;
Fisher, Donald A. ;
Gyi, Khin M. ;
Hodson, Margaret E. ;
Philips, Barbara J. ;
Baines, Deborah L. ;
Wood, David M. .
JOURNAL OF APPLIED PHYSIOLOGY, 2007, 102 (05) :1969-1975
[4]  
Bals Robert, 2004, J Cyst Fibros, V3 Suppl 2, P49, DOI 10.1016/j.jcf.2004.05.010
[5]   PULMONARY GLUCOSE-TRANSPORT IN THE FETAL SHEEP [J].
BARKER, PM ;
BOYD, CAR ;
RAMSDEN, CA ;
STRANG, LB ;
WALTERS, DV .
JOURNAL OF PHYSIOLOGY-LONDON, 1989, 409 :15-27
[6]   METABOLIC RESPONSE TO CARBON-MONOXIDE BY ISOLATED RAT LUNGS [J].
BASSETT, DJP ;
FISHER, AB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1976, 230 (03) :658-663
[7]   EFFECT OF HYPOXIA ON INCORPORATION OF GLUCOSE CARBONS INTO LIPIDS BY ISOLATED RAT LUNG [J].
BASSETT, DJP ;
FISHER, AB ;
RABINOWITZ, JL .
AMERICAN JOURNAL OF PHYSIOLOGY, 1974, 227 (05) :1103-1108
[8]   Characterization of ion and fluid transport in human bronchioles [J].
Blouquit, S ;
Morel, H ;
Hinnrasky, J ;
Naline, E ;
Puchelle, E ;
Chinet, T .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2002, 27 (04) :503-510
[9]   EVIDENCE FOR REDUCED CL- AND INCREASED NA+ PERMEABILITY IN CYSTIC-FIBROSIS HUMAN PRIMARY-CELL CULTURES [J].
BOUCHER, RC ;
COTTON, CU ;
GATZY, JT ;
KNOWLES, MR ;
YANKASKAS, JR .
JOURNAL OF PHYSIOLOGY-LONDON, 1988, 405 :77-103
[10]   ULTRASTRUCTURE OF AIRWAY EPITHELIAL-CELL MEMBRANES AMONG PATIENTS WITH CYSTIC-FIBROSIS [J].
CARSON, JL ;
COLLIER, AM ;
GAMBLING, TM ;
KNOWLES, MR ;
BOUCHER, RC .
HUMAN PATHOLOGY, 1990, 21 (06) :640-647