Testing the Hypothesis that System y+L Accounts for High- and Low-Transport Phenotypes in Chicken Erythrocytes Using L-Leucine as Substrate

Testing the Hypothesis that System y+L Accounts for High- and Low-Transport Phenotypes in Chicken... Experiments were carried out to test the hypothesis that system y+L accounts for the high (HT) and low (LT) amino-acid transport phenotypes in chicken erythrocytes and to explain the different effect of selective breeding on lysine and leucine fluxes. L-Leucine transport was characterized in individuals which had been separated into two groups (HT and LT) according to their capacity to transport L-lysine across the erythrocyte membrane. Whereas lysine influx (1 μM) in the two groups differed by 32-fold (HT/LT), leucine influx was not significantly different. Average rates (nmol/ L cells/ min) were: 227 (HT) and 7.0 (LT) for L-lysine, and 8.9 (HT) and 7.1 (LT) for L-leucine. The differential ability of L-lysine and L-leucine fluxes to discriminate between the HT and LT phenotypes was shown to be consistent with the interactions of these substrates with system y+L and to vary depending on the conditions of the assay. It is shown that the two phenotypes can be clearly discriminated by measuring L-leucine influx in the presence of Li+. These results support the hypothesis that the HT and LT phenotypes reflect alterations in the function of system y+L and illustrate that the choice of the appropriate substrate and medium composition must be carefully considered when investigating the consequences of either experimental or natural alterations of broad-scope transporters. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png The Journal of Membrane Biology Springer Journals

Testing the Hypothesis that System y+L Accounts for High- and Low-Transport Phenotypes in Chicken Erythrocytes Using L-Leucine as Substrate

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Publisher
Springer-Verlag
Copyright
Copyright © 2005 by Springer Science+Business Media, Inc.
Subject
Life Sciences; Human Physiology; Biochemistry, general
ISSN
0022-2631
eISSN
1432-1424
D.O.I.
10.1007/s00232-005-0751-x
Publisher site
See Article on Publisher Site

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