Comparison of ion transport by cultured secretory and absorptive canine airway epithelia

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Comparison of ion transport by cultured secretory and absorptive canine airway epithelia. / Boucher, R C; Larsen, Erik Hviid.

I: American Journal of Physiology (Consolidated), Bind 254, Nr. 4 Pt 1, 04.1988, s. C535-47.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Boucher, RC & Larsen, EH 1988, 'Comparison of ion transport by cultured secretory and absorptive canine airway epithelia', American Journal of Physiology (Consolidated), bind 254, nr. 4 Pt 1, s. C535-47.

APA

Boucher, R. C., & Larsen, E. H. (1988). Comparison of ion transport by cultured secretory and absorptive canine airway epithelia. American Journal of Physiology (Consolidated), 254(4 Pt 1), C535-47.

Vancouver

Boucher RC, Larsen EH. Comparison of ion transport by cultured secretory and absorptive canine airway epithelia. American Journal of Physiology (Consolidated). 1988 apr.;254(4 Pt 1):C535-47.

Author

Boucher, R C ; Larsen, Erik Hviid. / Comparison of ion transport by cultured secretory and absorptive canine airway epithelia. I: American Journal of Physiology (Consolidated). 1988 ; Bind 254, Nr. 4 Pt 1. s. C535-47.

Bibtex

@article{7377c1e0333c4d728d751ca39d6044d0,
title = "Comparison of ion transport by cultured secretory and absorptive canine airway epithelia",
abstract = "The use of primary cell culture techniques to predict the function of native respiratory epithelia was tested in studies of dog airway epithelia. Epithelial cells from Cl- secretory (tracheal) and Na+ absorptive (bronchial) airway regions were isolated by enzymatic digestion, plated on collagen matrices, and maintained in serum-free, hormone-supplemented media. Transepithelial and intracellular studies showed that both the tracheal and bronchial culture preparations exhibited bioelectric parameters quantitatively similar to those of intact tissues. Similar to the native tissue, the tracheal preparation exhibited an equivalent short-circuit circuit (Ieq) that was sensitive to inhibitors of Cl- transport (bumetanide, diphenylamine carboxylic acid) but was insensitive to an inhibitor of Na+ transport, amiloride. In contrast, the bronchial preparation, like the native tissue, exhibited an Ieq sensitive to amiloride but insensitive to bumetanide. As compared with the trachea, the bronchial (absorptive) epithelium is characterized by 1) a large amiloride-sensitive cellular conductance and 2) a relatively depolarized basolateral membrane. We conclude that this primary cell culture technique provides epithelial preparations comparable to the native tissue and suitable for quantitative studies of regional differences in ion transport function.",
keywords = "Amiloride, Animals, Bronchi, Bumetanide, Cell Adhesion, Cells, Cultured, Dogs, Epithelial Cells, Epithelium, Isoproterenol, Kinetics, Male, Membrane Potentials, Microscopy, Electron, Sodium, Trachea",
author = "Boucher, {R C} and Larsen, {Erik Hviid}",
year = "1988",
month = apr,
language = "English",
volume = "254",
pages = "C535--47",
journal = "American Journal of Physiology - Cell Physiology",
issn = "0363-6143",
publisher = "American Physiological Society",
number = "4 Pt 1",

}

RIS

TY - JOUR

T1 - Comparison of ion transport by cultured secretory and absorptive canine airway epithelia

AU - Boucher, R C

AU - Larsen, Erik Hviid

PY - 1988/4

Y1 - 1988/4

N2 - The use of primary cell culture techniques to predict the function of native respiratory epithelia was tested in studies of dog airway epithelia. Epithelial cells from Cl- secretory (tracheal) and Na+ absorptive (bronchial) airway regions were isolated by enzymatic digestion, plated on collagen matrices, and maintained in serum-free, hormone-supplemented media. Transepithelial and intracellular studies showed that both the tracheal and bronchial culture preparations exhibited bioelectric parameters quantitatively similar to those of intact tissues. Similar to the native tissue, the tracheal preparation exhibited an equivalent short-circuit circuit (Ieq) that was sensitive to inhibitors of Cl- transport (bumetanide, diphenylamine carboxylic acid) but was insensitive to an inhibitor of Na+ transport, amiloride. In contrast, the bronchial preparation, like the native tissue, exhibited an Ieq sensitive to amiloride but insensitive to bumetanide. As compared with the trachea, the bronchial (absorptive) epithelium is characterized by 1) a large amiloride-sensitive cellular conductance and 2) a relatively depolarized basolateral membrane. We conclude that this primary cell culture technique provides epithelial preparations comparable to the native tissue and suitable for quantitative studies of regional differences in ion transport function.

AB - The use of primary cell culture techniques to predict the function of native respiratory epithelia was tested in studies of dog airway epithelia. Epithelial cells from Cl- secretory (tracheal) and Na+ absorptive (bronchial) airway regions were isolated by enzymatic digestion, plated on collagen matrices, and maintained in serum-free, hormone-supplemented media. Transepithelial and intracellular studies showed that both the tracheal and bronchial culture preparations exhibited bioelectric parameters quantitatively similar to those of intact tissues. Similar to the native tissue, the tracheal preparation exhibited an equivalent short-circuit circuit (Ieq) that was sensitive to inhibitors of Cl- transport (bumetanide, diphenylamine carboxylic acid) but was insensitive to an inhibitor of Na+ transport, amiloride. In contrast, the bronchial preparation, like the native tissue, exhibited an Ieq sensitive to amiloride but insensitive to bumetanide. As compared with the trachea, the bronchial (absorptive) epithelium is characterized by 1) a large amiloride-sensitive cellular conductance and 2) a relatively depolarized basolateral membrane. We conclude that this primary cell culture technique provides epithelial preparations comparable to the native tissue and suitable for quantitative studies of regional differences in ion transport function.

KW - Amiloride

KW - Animals

KW - Bronchi

KW - Bumetanide

KW - Cell Adhesion

KW - Cells, Cultured

KW - Dogs

KW - Epithelial Cells

KW - Epithelium

KW - Isoproterenol

KW - Kinetics

KW - Male

KW - Membrane Potentials

KW - Microscopy, Electron

KW - Sodium

KW - Trachea

M3 - Journal article

C2 - 3354651

VL - 254

SP - C535-47

JO - American Journal of Physiology - Cell Physiology

JF - American Journal of Physiology - Cell Physiology

SN - 0363-6143

IS - 4 Pt 1

ER -

ID: 103934478