Skip to main content
Log in

Apical and basolateral membrane ionic channels in rabbit urinary bladder epithelium

  • Characterization of Ion Channels
  • Published:
Pflügers Archiv Aims and scope Submit manuscript

Abstract

This paper reviews the properties and regulation of single amiloride-sensitive Na+ channels in the apical membrane, and Cl and K+ channels in the basolateral membrane of rabbit urinary bladder. According to fluctuation analysis, there is an average of one amiloride-sensitive Na+ channel for every 40 μm2 of apical membrane. Each Na+ channel passes 0.7 pA of current under normal, short-circuit conditions. Apical channels are hydrolysed by the endogenous enzyme urokinase, which is released into the urine by the kidney. After exposure to urokinase, the Na+ channel loses its amiloride sensitivity, and eventually becomes unstable in the membrane. The selectivity and kinetic properties of single anion and K+ channels in the basolateral membrane were also studied using the patch clamp technique. The properties of these channels are discussed in terms of the regulation of transepithelial Na+ transport.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Hamill OP, Marty A, Neher E, Sakman B, Sigworth FJ (1981) Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflügers Arch 391:85–100

    Google Scholar 

  • Hanrahan JW, Alles WP, Lewis SA (1984) Basolateral anion and K+ channels from rabbit urinary bladder epithelium. J Gen Physiol 84:30a

    Google Scholar 

  • Hanrahan JW, Alles WP, Lewis SA (1985) Single basolateral K+ channels are expressed in primary cultures of urinary bladder epithelial cells. Biophys J (in press)

  • Hudson RL, Schultz SG (1984) Sodium coupled sugar transport: Effects of intracellular sodium activities and sodium-pump activity. Science 224:1237–1239

    Google Scholar 

  • Jorgensen PL (1975) Isolation and characterization of the components of the sodium pump. Quart Rev Biophys 7:239–274

    Google Scholar 

  • Koefoed-Johnson V, Ussing HH (1958) The nature of the frog skin potential. Acta Physiol Scand 42:298–308

    Google Scholar 

  • Lewis SA, de Moura JLC (1982) Incorporation of cytoplasmic vesicles into apical membrane of mammalian urinary bladder. Nature 297:685–688

    Google Scholar 

  • Lewis SA, Eaton DC, Diamond JM (1976) The mechanism of Na+ transport by rabbit urinary bladder. J Membr Biol 28: 41–70

    Google Scholar 

  • Lewis SA, Wills NK (1983) Apical membrane permeability and kinetic properties of the sodium pump in rabbit urinary bladder. J Physiol 341:169–184

    Google Scholar 

  • Lewis SA, Eaton DC, Clausen C, Diamond JM (1977) Nystatin as a probe for investigating the electrical properties of a tight epithelium. J Gen Physiol 70:427–440

    Google Scholar 

  • Lewis SA, Wills NK, Eaton DC (1978) Basolateral membrane potential of a tight epithelium: ionic diffusion and electrogenic pumps. J Memb Biol 41:117–148

    Google Scholar 

  • Lewis SA, Butt AG, Bowler MJ, Leader JP, MacKnight ADC (1984a) Anions modulate the basolateral membrane potassium conductance in toad urinary bladder. Biophys J 45:303a

    Google Scholar 

  • Lewis SA, Ifshin MS, Loo DDF, Diamond JM (1984b) Studies of sodium channels in rabbit urinary bladder by noise analysis. J Membr Biol 80:135–151

    Google Scholar 

  • Lindemann B, Van Driessche W (1977) Sodium-specific membrane channels of frog skin are pores: Current fluctuations reveal high turnover. Science 195:292–294

    Google Scholar 

  • Minsky BD, Chlapowski FJ (1978) Morphometric analysis of the translocation of luminal membrane between cytoplasm and cell surface of transitional epithelial cells during the expansion-contraction cycles of mammalian urinary bladder. J Cell Biol 77:685–697

    Google Scholar 

  • Neher E, Stevens CF (1977) Conductance fluctuations and ionic pores in membranes. Ann Rev Biophys Bioeng 6:345–381

    Google Scholar 

  • Schneider BH, Bachmann F, Sauser D (1982) Urokinase. A short review of its properties and of its metabolism. In: Mannucci PM, D'Angelo A (eds) Urokinase: basic and clinical aspects, chapter 1. Academic Press, New York, p 1

    Google Scholar 

  • Staehelin LA, Chlapowski FJ, Bonneville MA (1972) Luminal plasma membrane of the urinary bladder. I. Three-dimensional reconstruction from freeze-etch images. J Cell Biol 53:73–91

    Google Scholar 

  • Wills NK, Lewis SA (1980) Intracellular Na+ activity as a function of Na+ transport rate across a tight epithelium. Biophys J 30:181–186

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lewis, S.A., Hanrahan, J.W. Apical and basolateral membrane ionic channels in rabbit urinary bladder epithelium. Pflugers Arch. 405 (Suppl 1), S83–S88 (1985). https://doi.org/10.1007/BF00581785

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00581785

Key words

Navigation