Membrane permeability of an epithelial cell junction (Drosophila salivary gland) was examined with intracellular microelectrodes and with fluorescent tracers. In contrast to the non-junctional cell membrane surface, which has a low permeability to ions (10-4 mho/cm2), the junctional membrane surface is highly permeable. In fact, it introduces no substantial restriction to ion flow beyond that in the cytoplasm; the resistance through a chain of cells (150 Ω cm) is only slightly greater than in extruded cytoplasm (100 Ω cm). The diffusion resistance along the intercellular space to the exterior, on the other hand, is very high. Here, there exists an ion barrier of, at least, 104Ω cm2. As a result, small ions and fluorescein move rather freely from one cell to the next, but do not leak appreciably through the intercellular space to the exterior. The organ here, rather than the single cell, appears to be the unit of ion environment. The possible underlying structural aspects are discussed.
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1 September 1964
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September 01 1964
STUDIES ON AN EPITHELIAL (GLAND) CELL JUNCTION : I. Modifications of Surface Membrane Permeability
Werner R. Loewenstein,
Werner R. Loewenstein
From the Department of Physiology, Columbia University, College of Physicians and Surgeons, New York
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Yoshinobu Kanno
Yoshinobu Kanno
From the Department of Physiology, Columbia University, College of Physicians and Surgeons, New York
Search for other works by this author on:
Werner R. Loewenstein
From the Department of Physiology, Columbia University, College of Physicians and Surgeons, New York
Yoshinobu Kanno
From the Department of Physiology, Columbia University, College of Physicians and Surgeons, New York
Received:
November 13 1963
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1964 by The Rockefeller Institute Press
1964
J Cell Biol (1964) 22 (3): 565–586.
Article history
Received:
November 13 1963
Citation
Werner R. Loewenstein, Yoshinobu Kanno; STUDIES ON AN EPITHELIAL (GLAND) CELL JUNCTION : I. Modifications of Surface Membrane Permeability . J Cell Biol 1 September 1964; 22 (3): 565–586. doi: https://doi.org/10.1083/jcb.22.3.565
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