Intestinal Transport of Cystine and Cysteine in Man: Evidence for Separate Mechanisms*
Open Access
- 1 January 1967
- journal article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 46 (1) , 30-34
- https://doi.org/10.1172/jci105508
Abstract
Cystine and cysteine are transported by energy-dependent, mediated processes in human gut. When either of these amino acids is transported, only cysteine is recovered intracellularly, indicating that cystine is reduced to cysteine after achieving an intracellular location. In contrast to results with cystine, cysteine uptake is not defective in gut from cystinuric patients, nor do lysine and arginine compete with cysteine for transport. It is, therefore, concluded that cystine and cysteine are transported by different mechanisms, and that only the cystine transport mechanism is defective in cystinuria.Keywords
This publication has 11 references indexed in Scilit:
- Dithiothreitol in the study of cysteine transportBiochimica et Biophysica Acta (BBA) - General Subjects, 1966
- Cystinuria: biochemical evidence for three genetically distinct diseases.Journal of Clinical Investigation, 1966
- Intestinal Absorption and Renal Extraction of Cystine and Cysteine in CystinuriaNew England Journal of Medicine, 1965
- Cysteine metabolism in cystinuria.1965
- Cystine metabolism in cystinuria.1965
- Cystinuria: Defective Intestinal Transport of Dibasic Amino Acids and Cystine*Journal of Clinical Investigation, 1965
- Defective Uptake of Basic Amino Acids and l-Cystine by Intestinal Mucosa of Patients with Cystinuria *Journal of Clinical Investigation, 1964
- Evidence against a Single Renal Transport Defect in CystinuriaNew England Journal of Medicine, 1964
- Competitive Inhibition of Dibasic Amino Acid Transport in Rat KidneyJournal of Biological Chemistry, 1962
- The absorption of cystine and cysteine from rat small intestineBiochemical Journal, 1959