Isolated cortical collecting tubules from rabbit kidney were studied during perfusion with solutions made either isotonic or hypotonic to the external bathing medium. Examination of living tubules revealed a reversible increase in thickness of the cellular layer, prominence of lateral cell membranes, and formation of intracellular vacuoles during periods of vasopressin-induced osmotic water transport. Examination in the electron microscope revealed that vasopressin induced no changes in cell structure in collecting tubules in the absence of an osmotic difference and significant bulk water flow across the tubule wall. In contrast, tubules fixed during vasopressin-induced periods of high osmotic water transport showed prominent dilatation of lateral intercellular spaces, bulging of apical cell membranes into the tubular lumen, and formation of intracellular vacuoles. It is concluded that the ultrastructural changes are secondary to transepithelial bulk water flow and not to a direct effect of vasopressin on the cells, and that vasopressin induces osmotic flow by increasing water permeability of the luminal cell membrane. The lateral intercellular spaces may be part of the pathway for osmotically induced transepithelial bulk water flow.
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1 February 1968
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February 01 1968
ULTRASTRUCTURAL STUDIES OF VASOPRESSIN EFFECT ON ISOLATED PERFUSED RENAL COLLECTING TUBULES OF THE RABBIT
Charles E. Ganote,
Charles E. Ganote
From the Laboratory of Experimental Pathology, National Institute of Arthritis and Metabolic Diseases, and the Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Service, United States Department of Health, Education, and Welfare, Bethesda, Maryland 20014
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Jared J. Grantham,
Jared J. Grantham
From the Laboratory of Experimental Pathology, National Institute of Arthritis and Metabolic Diseases, and the Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Service, United States Department of Health, Education, and Welfare, Bethesda, Maryland 20014
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Harold L. Moses,
Harold L. Moses
From the Laboratory of Experimental Pathology, National Institute of Arthritis and Metabolic Diseases, and the Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Service, United States Department of Health, Education, and Welfare, Bethesda, Maryland 20014
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Maurice B. Burg,
Maurice B. Burg
From the Laboratory of Experimental Pathology, National Institute of Arthritis and Metabolic Diseases, and the Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Service, United States Department of Health, Education, and Welfare, Bethesda, Maryland 20014
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Jack Orloff
Jack Orloff
From the Laboratory of Experimental Pathology, National Institute of Arthritis and Metabolic Diseases, and the Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Service, United States Department of Health, Education, and Welfare, Bethesda, Maryland 20014
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Charles E. Ganote
From the Laboratory of Experimental Pathology, National Institute of Arthritis and Metabolic Diseases, and the Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Service, United States Department of Health, Education, and Welfare, Bethesda, Maryland 20014
Jared J. Grantham
From the Laboratory of Experimental Pathology, National Institute of Arthritis and Metabolic Diseases, and the Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Service, United States Department of Health, Education, and Welfare, Bethesda, Maryland 20014
Harold L. Moses
From the Laboratory of Experimental Pathology, National Institute of Arthritis and Metabolic Diseases, and the Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Service, United States Department of Health, Education, and Welfare, Bethesda, Maryland 20014
Maurice B. Burg
From the Laboratory of Experimental Pathology, National Institute of Arthritis and Metabolic Diseases, and the Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Service, United States Department of Health, Education, and Welfare, Bethesda, Maryland 20014
Jack Orloff
From the Laboratory of Experimental Pathology, National Institute of Arthritis and Metabolic Diseases, and the Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Service, United States Department of Health, Education, and Welfare, Bethesda, Maryland 20014
Received:
August 22 1967
Revision Received:
October 02 1967
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1968 by The Rockefeller University Press
1968
J Cell Biol (1968) 36 (2): 355–367.
Article history
Received:
August 22 1967
Revision Received:
October 02 1967
Citation
Charles E. Ganote, Jared J. Grantham, Harold L. Moses, Maurice B. Burg, Jack Orloff; ULTRASTRUCTURAL STUDIES OF VASOPRESSIN EFFECT ON ISOLATED PERFUSED RENAL COLLECTING TUBULES OF THE RABBIT . J Cell Biol 1 February 1968; 36 (2): 355–367. doi: https://doi.org/10.1083/jcb.36.2.355
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