Skip to main content
The Journal of Biophysical and Biochemical Cytology logoLink to The Journal of Biophysical and Biochemical Cytology
. 1961 Aug 1;10(4):529–553. doi: 10.1083/jcb.10.4.529

STRUCTURE OF THE TOAD'S URINARY BLADDER AS RELATED TO ITS PHYSIOLOGY

Lee D Peachey 1, Howard Rasmussen 1
PMCID: PMC2225090  PMID: 13733732

Abstract

The structure of the urinary bladder of the toad Bufo marinus was studied by light and electron microscopy. The epithelium covering the mucosal surface of the bladder is 3 to 10 microns thick and consists of squamous epithelial cells, goblet cells, and a third class of cells containing many mitochondria and possibly representing goblet cells in early stages of their secretory cycle. This epithelium is supported on a lamina propria 30 to several hundred microns thick and containing collagen fibrils, bundles of smooth muscle fibers, and blood vessels. The serosal surface of the bladder is covered by an incomplete mesothelium. The cytoplasm of the squamous epithelial cells, which greatly outnumber the other types of cells, is organized in a way characteristic of epithelial secretory cells. Mitochondria, smooth and rough surfaced endoplasmic reticulum, a Golgi apparatus, "multivesicular bodies," and isolated particles and vesicles are present. Secretion granules are found immediately under the plasma membranes of the free surfaces of the epithelial cells and are seen to fuse with these membranes and release their contents to contribute to a fibrous surface coating found only on the free mucosal surfaces of the cells. Beneath the plasma membranes on these surfaces is an additional, finely granular component. Lateral and basal plasma membranes are heavily plicated and appear ordinary in fine structure. The cells of the epithelium are tightly held together by a terminal bar apparatus and sealed together, with an intervening space of only 0.02 mµ near the bladder lumen, in such a way as to prevent water leakage between the cells. It is demonstrated in in vitro experiments that water traversing the bladder wall passes through the cytoplasm of the epithelial cells and that a vesicle transport mechanism is not involved. In vitro experiments also show that the basal (serosal) surfaces of the epithelial cells are freely permeable to water, while the free (mucosal) surfaces are normally relatively impermeable but become permeable when the serosal surface of the bladder is treated with neurohypophyseal hormones. The permeability barrier found at the mucosal surface may be represented, structurally, either by the filamentous layer lying external to the plasma membrane, by the intracellular, granular component found just under the plasma membrane, or by both of these components of the mucosal surface complex. The polarity of the epithelial sheet is emphasized and related to the physiological role of the urinary bladder in amphibian water balance mechanisms.

Full Text

The Full Text of this article is available as a PDF (2.6 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BARRNETT R. J., BALL E. G. Metabolic and ultrastructural changes induced in adipose tissue by insulin. J Biophys Biochem Cytol. 1960 Sep;8:83–101. doi: 10.1083/jcb.8.1.83. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BENTLEY P. J. The effects of neurohypophysial extracts on the water transfer across the wall of the isolated urinary bladder of the toad Bufo marinus. J Endocrinol. 1958 Sep;17(3):201–209. doi: 10.1677/joe.0.0170201. [DOI] [PubMed] [Google Scholar]
  3. HUXLEY A. F. Local activation of striated muscle from the frog and the crab. J Physiol. 1957 Jan 23;135(1):17–8P. [PubMed] [Google Scholar]
  4. LEAF A., ANDERSON J., PAGE L. B. Active sodium transport by the isolated toad bladder. J Gen Physiol. 1958 Mar 20;41(4):657–668. doi: 10.1085/jgp.41.4.657. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. LEAF A., PAGE L. B., ANDERSON J. Respiration and active sodium transport of isolated toad bladder. J Biol Chem. 1959 Jun;234(6):1625–1629. [PubMed] [Google Scholar]
  6. LEAF A. Some actions of neurohypophyseal hormones on a living membrane. J Gen Physiol. 1960 May;43:175–189. doi: 10.1085/jgp.43.5.175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. LEAF A. The mechanism of the asymmetrical distribution of endogenous lactate about the isolated toad bladder. J Cell Comp Physiol. 1959 Aug;54:103–108. doi: 10.1002/jcp.1030540111. [DOI] [PubMed] [Google Scholar]
  8. MAFFLY R. H., HAYS R. M., LAMDIN E., LEAF A. The effect of neurohypophyseal hormones on the permeability of the toad bladder to urea. J Clin Invest. 1960 Apr;39:630–641. doi: 10.1172/JCI104078. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. MOORE D. H., RUSKA H. The fine structure of capillaries and small arteries. J Biophys Biochem Cytol. 1957 May 25;3(3):457–462. doi: 10.1083/jcb.3.3.457. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. ODLAND G. F. The fine structure of the interrelationship of cells in the human epidermis. J Biophys Biochem Cytol. 1958 Sep 25;4(5):529–538. [PMC free article] [PubMed] [Google Scholar]
  11. PAK POY R. F., BENTLEY P. J. Fine structure of the epithelial cells of the toad urinary bladder. Exp Cell Res. 1960 Jun;20:235–237. doi: 10.1016/0014-4827(60)90246-9. [DOI] [PubMed] [Google Scholar]
  12. PALADE G. E. A study of fixation for electron microscopy. J Exp Med. 1952 Mar;95(3):285–298. doi: 10.1084/jem.95.3.285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. PORTER K. R., BLUM J. A study in microtomy for electron microscopy. Anat Rec. 1953 Dec;117(4):685–710. doi: 10.1002/ar.1091170403. [DOI] [PubMed] [Google Scholar]
  14. RHODIN J., DALHAMN T. Electron microscopy of the tracheal ciliated mucosa in rat. Z Zellforsch Mikrosk Anat. 1956;44(4):345–412. doi: 10.1007/BF00345847. [DOI] [PubMed] [Google Scholar]
  15. RUSKA C. [The cell structures of the epithelium of the small intestine in their dependence on the physico-chemical character of the intestinal content. I. Water and sodium chloride]. Z Zellforsch Mikrosk Anat. 1960;52:748–777. [PubMed] [Google Scholar]
  16. Rasmussen H., Schwartz I. L., Schoessler M. A., Hochster G. STUDIES ON THE MECHANISM OF ACTION OF VASOPRESSIN. Proc Natl Acad Sci U S A. 1960 Oct;46(10):1278–1287. doi: 10.1073/pnas.46.10.1278. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. SAWYER W. H. Increased water permeability of the bullfrog (Rana catesbiana) bladder in vitro in response to synthetic oxytocin and arginine vasotocin and to neurohypophysial extracts from nomammalian vertebrates. Endocrinology. 1960 Jan;66:112–120. doi: 10.1210/endo-66-1-112. [DOI] [PubMed] [Google Scholar]
  18. SOTELO J. R., PORTER K. R. An electron microscope study of the rat ovum. J Biophys Biochem Cytol. 1959 Mar 25;5(2):327–342. doi: 10.1083/jcb.5.2.327. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Biophysical and Biochemical Cytology are provided here courtesy of The Rockefeller University Press

RESOURCES