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Desialation of transferrin by rat liver endothelium

Journal Article · · J. Clin. Invest.; (United States)
DOI:https://doi.org/10.1172/JCI113625· OSTI ID:7074916

To examine the role of liver endothelium in desialation of transferrin (TF), pulse-chase studies were done by incubation of either /sup 3/H (sialic acid labeled)-, or /sup 125/I, or /sup 59/Fe (protein core labeled)-TF with fractionated liver endothelium. While /sup 125/I or /sup 59/Fe labels were externalized after initial binding and internalization, a large proportion of 3H label was internalized and remained within the cell. When the supernatant of these experiments was studied by isoelectricfocusing and Ricinus communis agglutinin (RCA120) affinity chromatography, generation of asialotransferrin was noted by both techniques. Incubation of liver endothelium with double-labeled TF (sialic acids with /sup 3/H and protein core with /sup 125/I or /sup 59/Fe) led initially to a concordant uptake of the two labels, which were then dissociated and /sup 3/H was retained by the cell. These findings indicate desialation of TF by liver endothelium. The significance of these findings in the pathogenesis of hepatic siderosis is discussed.

Research Organization:
Veterans Administration Medical Center, Jackson, MS (USA)
OSTI ID:
7074916
Journal Information:
J. Clin. Invest.; (United States), Journal Name: J. Clin. Invest.; (United States) Vol. 82:2; ISSN JCINA
Country of Publication:
United States
Language:
English