Cargando…

Airway Surface Liquid Osmolality Measured Using Fluorophore-Encapsulated Liposomes

The airway surface liquid (ASL) is the thin layer of fluid coating the luminal surface of airway epithelial cells at an air interface. Its composition and osmolality are thought to be important in normal airway physiology and in airway diseases such as asthma and cystic fibrosis. The determinants of...

Descripción completa

Detalles Bibliográficos
Autores principales: Jayaraman, Sujatha, Song, Yuanlin, Verkman, A.S.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2233658/
https://www.ncbi.nlm.nih.gov/pubmed/11331352
_version_ 1782150276769120256
author Jayaraman, Sujatha
Song, Yuanlin
Verkman, A.S.
author_facet Jayaraman, Sujatha
Song, Yuanlin
Verkman, A.S.
author_sort Jayaraman, Sujatha
collection PubMed
description The airway surface liquid (ASL) is the thin layer of fluid coating the luminal surface of airway epithelial cells at an air interface. Its composition and osmolality are thought to be important in normal airway physiology and in airway diseases such as asthma and cystic fibrosis. The determinants of ASL osmolality include epithelial cell solute and water transport properties, evaporative water loss, and the composition of secreted fluids. We developed a noninvasive approach to measure ASL osmolality using osmotically sensitive 400-nm-diam liposomes composed of phosphatidylcholine/cholesterol/polyethylene glycol-phosphatidylcholine (1:0.3:0.08 molar ratio). Calcein was encapsulated in the liposomes at self-quenching concentrations (30 mM) as a volume-sensitive marker, together with sulforhodamine 101 (2 mM) as a volume-insensitive reference. Liposome calcein/sulforhodamine 101 fluorescence ratios responded rapidly (<0.2 s) and stably to changes in solution osmolality. ASL osmolality was determined from calcein/sulforhodamine 101 fluorescence ratios after addition of microliter quantities of liposome suspensions to the ASL. In bovine airway epithelial cells cultured on porous supports at an air–liquid interface, ASL thickness (by confocal microscopy) was 22 μm and osmolality was 325 ± 12 mOsm. In anesthetized mice in which a transparent window was created in the trachea, ASL thickness was 55 μm and osmolality was 330 ± 36 mOsm. ASL osmolality was not affected by pharmacological inhibition of CFTR in airway cell cultures or by genetic deletion of CFTR in knockout mice. ASL osmolality could be increased substantially to >400 mOsm by exposure of the epithelium to dry air; the data were modeled mathematically using measured rates of osmosis and evaporative water loss. These results establish a ratio imaging method to map osmolality in biological compartments. ASL fluid is approximately isosmolar under normal physiological conditions, but can become hyperosmolar when exposed to dry air, which may induce cough and airway reactivity in some patients.
format Text
id pubmed-2233658
institution National Center for Biotechnology Information
language English
publishDate 2001
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-22336582008-04-21 Airway Surface Liquid Osmolality Measured Using Fluorophore-Encapsulated Liposomes Jayaraman, Sujatha Song, Yuanlin Verkman, A.S. J Gen Physiol Original Article The airway surface liquid (ASL) is the thin layer of fluid coating the luminal surface of airway epithelial cells at an air interface. Its composition and osmolality are thought to be important in normal airway physiology and in airway diseases such as asthma and cystic fibrosis. The determinants of ASL osmolality include epithelial cell solute and water transport properties, evaporative water loss, and the composition of secreted fluids. We developed a noninvasive approach to measure ASL osmolality using osmotically sensitive 400-nm-diam liposomes composed of phosphatidylcholine/cholesterol/polyethylene glycol-phosphatidylcholine (1:0.3:0.08 molar ratio). Calcein was encapsulated in the liposomes at self-quenching concentrations (30 mM) as a volume-sensitive marker, together with sulforhodamine 101 (2 mM) as a volume-insensitive reference. Liposome calcein/sulforhodamine 101 fluorescence ratios responded rapidly (<0.2 s) and stably to changes in solution osmolality. ASL osmolality was determined from calcein/sulforhodamine 101 fluorescence ratios after addition of microliter quantities of liposome suspensions to the ASL. In bovine airway epithelial cells cultured on porous supports at an air–liquid interface, ASL thickness (by confocal microscopy) was 22 μm and osmolality was 325 ± 12 mOsm. In anesthetized mice in which a transparent window was created in the trachea, ASL thickness was 55 μm and osmolality was 330 ± 36 mOsm. ASL osmolality was not affected by pharmacological inhibition of CFTR in airway cell cultures or by genetic deletion of CFTR in knockout mice. ASL osmolality could be increased substantially to >400 mOsm by exposure of the epithelium to dry air; the data were modeled mathematically using measured rates of osmosis and evaporative water loss. These results establish a ratio imaging method to map osmolality in biological compartments. ASL fluid is approximately isosmolar under normal physiological conditions, but can become hyperosmolar when exposed to dry air, which may induce cough and airway reactivity in some patients. The Rockefeller University Press 2001-05-01 /pmc/articles/PMC2233658/ /pubmed/11331352 Text en © 2001 The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Original Article
Jayaraman, Sujatha
Song, Yuanlin
Verkman, A.S.
Airway Surface Liquid Osmolality Measured Using Fluorophore-Encapsulated Liposomes
title Airway Surface Liquid Osmolality Measured Using Fluorophore-Encapsulated Liposomes
title_full Airway Surface Liquid Osmolality Measured Using Fluorophore-Encapsulated Liposomes
title_fullStr Airway Surface Liquid Osmolality Measured Using Fluorophore-Encapsulated Liposomes
title_full_unstemmed Airway Surface Liquid Osmolality Measured Using Fluorophore-Encapsulated Liposomes
title_short Airway Surface Liquid Osmolality Measured Using Fluorophore-Encapsulated Liposomes
title_sort airway surface liquid osmolality measured using fluorophore-encapsulated liposomes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2233658/
https://www.ncbi.nlm.nih.gov/pubmed/11331352
work_keys_str_mv AT jayaramansujatha airwaysurfaceliquidosmolalitymeasuredusingfluorophoreencapsulatedliposomes
AT songyuanlin airwaysurfaceliquidosmolalitymeasuredusingfluorophoreencapsulatedliposomes
AT verkmanas airwaysurfaceliquidosmolalitymeasuredusingfluorophoreencapsulatedliposomes