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Journal of Experimental Biology, Vol 202, Issue 21 3003-3010, Copyright © 1999 by Company of Biologists
JOURNAL ARTICLES |
MK Monteilh-Zoller, V Zonno, C Storelli and GA Ahearn
Department of Zoology, University of Hawaii at Manoa, Honolulu, Hawaii 96822, USA and Laboratorio di Fisiologia, Departimento di Biologia, Universita di Lecce, Italy. ahearn@zoology.hawaii.edu
Epithelial brush-border membrane vesicles (BBMVs) from the hepatopancreas of the lobster Homarus americanus were prepared using a magnesium precipitation technique and employed in transport experiments designed to demonstrate the effects of external and internal divalent cationic heavy metals on the uptake of l-[(3)H]proline. When BBMVs were exposed to a high external concentration (2.5 mmol l(-)(1)) of Cd(2+), Cu(2+), Fe(2+), Mn(2+) or Zn(2+), l-[(3)H]proline (0.5 mmol l(-)(1)) uptake was significantly (P<0.05) decreased by each metal. However, if a 30 min pre-incubation period with each metal was used before incubation of the vesicles with amino acid and metal, a significant (P<0.05) enhancement of l-[(3)H]proline transport occurred. Zinc was the most stimulatory metal of those tested. Proline influxes (1.0 and 2.5 mmol l(-)(1)) were hyperbolic functions of bilateral [Zn(2+)], with a lower apparent zinc half-saturation constant (K(m)) at the higher amino acid concentration. l-[(3)H]proline influx was a hyperbolic function of external [l-proline] (K(m)=2.10+/-0.26 mmol l(-)(1); J(max)=2290+/-600 pmol mg(-)(1 )protein 10 s(-)(1)) (means +/- s.e.m., N=3), and bilateral exposure to zinc significantly (P<0.05) increased the maximal rate of influx, J(max), of proline (J(max)=4890+/-250 pmol mg(-)(1 )protein 10 s(-)(1)), but had no effect (P>0.05) on apparent l-[(3)H]proline binding to the membranes (K(m)=1.66+/-0.23 mmol l(-)(1)) (means +/- s.e.m., N=3). In the presence of 0.5 mmol l(-)(1 )l-pipecolate, bilateral zinc-stimulated, carrier-mediated, l-[(3)H]proline influx was abolished. At low external concentrations of zinc alone (e.g. below 1.0 mmol l(-)(1)), l-[(3)H]proline influx was enhanced by the metal. Enhanced amino acid uptake in the presence of external zinc alone was abolished by l-pipecolate. A model accounting for external and internal zinc enhancements of l-[(3)H]proline influx by the Na(+)-dependent l-pipecolate-sensitive IMINO transport system in these membranes is proposed.
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