Literature DB >> 6600738

Heteropore populations of bullfrog alveolar epithelium.

K J Kim, E D Crandall.   

Abstract

Diffusional fluxes of a large number of hydrophilic solutes and water across bullfrog (Rana catesbeiana) alveolar epithelium were measured in the Ussing-type flux chamber. Lungs were isolated from double-pithed animals and studied as flat sheets. Radioactive solutes and water were added to the upstream reservoir, and the rate of change of downstream reservoir radioactivity was monitored. A permeability coefficient was estimated for each substance from a linear relationship between radiotracer concentration in the downstream reservoir and time. These permeability data were used to analyze the equivalent water-filled pore characteristics of the alveolar epithelial barrier. The data reveal that the alveolar epithelium is best characterized by two distinct pore populations rather than by a single homogeneous pore population. The large-pore population consists of pores with a radius of about 5 nm and occupies 4% of the available pore area. The small-pore population consists of pores with a radius of about 0.5 nm and occupies 96% of the available pore area. The number of small pores to large pores is 2.68 X 10(3). After the alveolar surface was damaged by acid, a large-pore population with a radius of about 27 nm was seen, allowing nearly free diffusion of solutes. A major implication of the presence of two populations of pores in the alveolar epithelium is that hydrostatically driven bulk water flow occurs predominantly through the large pores, while osmotically driven bulk water flow takes place predominantly through the small pores. As a result, in general, hydrostatic and osmotic gradients may not be equally effective driving forces for water flow across this tissue.

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Year:  1983        PMID: 6600738     DOI: 10.1152/jappl.1983.54.1.140

Source DB:  PubMed          Journal:  J Appl Physiol Respir Environ Exerc Physiol        ISSN: 0161-7567


  13 in total

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5.  Horseradish peroxidase transport across rat alveolar epithelial cell monolayers.

Authors:  Y Matsukawa; H Yamahara; V H Lee; E D Crandall; K J Kim
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6.  Dipeptide transport across rat alveolar epithelial cell monolayers.

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7.  MAPK activation modulates permeability of isolated rat alveolar epithelial cell monolayers following cyclic stretch.

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9.  Disease Models: Lung Models for Testing Drugs Against Inflammation and Infection.

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10.  Tracking translocation of industrially relevant engineered nanomaterials (ENMs) across alveolar epithelial monolayers in vitro.

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