spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by WRIGHT, S. H.
Right arrow Articles by BRADLEY, T. J.
Right arrow Search for Related Content
PubMed
Right arrow Articles by WRIGHT, S. H.
Right arrow Articles by BRADLEY, T. J.
Journal of Experimental Biology 129,205-230 (1987)
Published by Company of Biologists 1987


Apical Membrane Permeability of Mytilus Gill: Influence of Ultrastructure, Salinity and Competitive Inhibitors on Amino Acid Fluxes

STEPHEN H. WRIGHT 1, TIMOTHY W. SECOMB 1, and TIMOTHY J. BRADLEY 2

1 Department of Physiology, College of Medicine, University of Arizona, Tucson AZ 85724, USA
2 Department of Development and Cell Biology, University of California, Irvine, CA 92717, USA

The apical membrane of gill integumental cells from the mussels Mytilus edulis and M. californianus serves as a permeability barrier separating sea water from a cytoplasm rich in amino acids and other small organic molecules. Morphometric analysis of transmission electronmicrographs indicates that the membrane area of these cells is increased between 10- and 18-fold by the presence of a microvillous brush border. The microvilli do not appear to influence the kinetics of solute transport across the cell apex, as determined using a mathematical model of the relationship between membrane structure and the kinetics of transport. Rates of amino acid loss from the integument were low, and estimates of the upper limit of the passive permeability of the apical membrane to amino acids ranged from 0.5 to 10x10-10 cm s-1. Abrupt exposure of intact mussels or isolated gill tissue to 60% sea water (19% salinity) resulted in a transient, 40- to 80-fold increase in the rate of loss of all amino acids from integumental tissues. Upon exposure to full-strength sea water, efflux rates returned to near control values. Exposure to 60% sea water also inhibited the carrier-mediated accumulation of amino acid: uptake of 0.5 µmol1-1 [14C]alanine and [14C]taurine was reduced by 80% compared to control uptake in 100% sea water. This inhibition was not adequate to account for the increase in net efflux of taurine from gill tissue into 60% artificial sea water (ASW), though the inhibition of alanine uptake may have contributed significantly to the increased loss of this amino acid. Efflux of discrete structural classes of amino acid occurred when integumental tissues were exposed to 50 µmoll-1 concentrations of structurally related analogues. It is concluded that the apical membrane of gill cells has a very low passive permeability to amino acids, and that the overall permeability of the gill can be increased in a reversible fashion by exposure to reduced salinity or to high external concentrations of amino acid.

Key words: transport, amino acid, integument, Mytilus, gill, epithelia

Accepted on November 6, 1986







© The Company of Biologists Ltd 1987