Monteilh-Zoller MK, Zonno V, Storelli C, Ahearn GA
Department of Zoology, University of Hawaii at Manoa, Honolulu, Hawaii 96822, USA and Laboratorio di Fisiologia, Departimento di Biologia, Universita di Lecce, Italy.
J Exp Biol. 1999;202(Pt 21):3003-3010. doi: 10.1242/jeb.202.21.3003.
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.