» Articles » PMID: 4326455

Correlation Between Pinocytosis and Hydroosmosis Induced by Neurohypophyseal Hormones and Mediated by Adenosine 3',5'-cyclic Monophosphate

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 1971 Jun 1
PMID 4326455
Citations 33
Authors
Affiliations
Soon will be listed here.
Abstract

The isolated urinary bladder of the toad responds to neurohypophyseal hormone with a net increase of water transport from the mucosal to the serosal solution in the presence of an osmotic gradient. This response is mediated intracellularly by cyclic 3',5'-adenosine monophosphate (AMP). The present study demonstrates that hydroosmotically active substances such as oxytocin, dibutyryl cyclic 3',5'-AMP, and theophylline, but not hydroosmotically inactive substances, induce the uptake of horseradish peroxidase from the mucosal solution. Peroxidase taken up by the mucosal cells is demonstrable in small tubules and vesicles, and eventually accumulates in lysosomes. The uptake of peroxidase from the serosal solution into similar bodies in the mucosal cells is not hormone-dependent. It is also shown that peroxidase does not penetrate the tight junction from either the mucosal or serosal solution. These results extend previous findings which implicated the apical membrane of the mucosal epithelium as the site affected by neurohypophyseal hormones. A mechanism based on secretory phenomena is proposed as a framework for future investigations of apical membrane permeability changes and pinocytosis.

Citing Articles

Evidence for the sorting of endocytic vesicle contents during the receptor-mediated transport of IgG across the newborn rat intestine.

Abrahamson D, Rodewald R J Cell Biol. 1981; 91(1):270-80.

PMID: 7298722 PMC: 2111928. DOI: 10.1083/jcb.91.1.270.


Multiple localizations of adenylate cyclase in rat hippocampus. A histochemical study.

Poeggel G, LUPPA H, Weiss J Histochemistry. 1982; 74(1):139-47.

PMID: 7085346 DOI: 10.1007/BF00495059.


Electron-microscopic and morphometric study of vesiculation in the epithelial cell layer of the toad urinary bladder. Effect of antidiuretic hormone.

Davis W, Jones R, Ciumei J, Knight J, GOODMAN D Cell Tissue Res. 1982; 225(3):619-31.

PMID: 6812956 DOI: 10.1007/BF00214808.


Quantitative analysis of exocytosis and endocytosis in the hydroosmotic response of toad bladder.

Gronowicz G, Masur S, Holtzman E J Membr Biol. 1980; 52(3):221-35.

PMID: 6770096 DOI: 10.1007/BF01869191.


Evidence that ADH-stimulated intramembrane particle aggregates are transferred from cytoplasmic to luminal membranes in toad bladder epithelial cells.

Muller J, Kachadorian W, DiScala V J Cell Biol. 1980; 85(1):83-95.

PMID: 6767731 PMC: 2110591. DOI: 10.1083/jcb.85.1.83.


References
1.
Manning M . Synthesis by the Merrifield method of a protected nonapeptide amide with the amino acid sequence of oxytocin. J Am Chem Soc. 1968; 90(5):1348-9. DOI: 10.1021/ja01007a041. View

2.
LUFT J . Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961; 9:409-14. PMC: 2224998. DOI: 10.1083/jcb.9.2.409. View

3.
Dibona D, Civan M . Toad urinary bladder: intercellular spaces. Science. 1969; 165(3892):503-4. DOI: 10.1126/science.165.3892.503. View

4.
Eggena P, SCHWARTZ I, Walter R . A sensitive hydroosmotic toad bladder assay. Affinity and intrinsic activity of neurohypophyseal peptides. J Gen Physiol. 1968; 52(3):465-81. PMC: 2225828. DOI: 10.1085/jgp.52.3.465. View

5.
GRAHAM Jr R, Karnovsky M . The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique. J Histochem Cytochem. 1966; 14(4):291-302. DOI: 10.1177/14.4.291. View