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The Role of Sialic Acid in Determining the Survival of Glycoproteins in the Circulation

Anatol G. Morell 1, Gregory Gregoriadis 1, I. Herbert Scheinberg 1, Jean Hickman 2, and Gilbert Ashwell 2

From the 1 From the Department of Medicine, Albert Einstein College of Medicine, New York, New York 10461
2 From the National Institute of Arthritis and Metabolic Diseases, National Institutes of Health, Bethesda, Maryland 20014

Evidence is presented to indicate a generalized role for the terminal sialic acid residues of circulating glycoproteins. Upon injection into rats, all of the desialylated plasma proteins tested, with the exception of transferrin, were promptly removed from the circulation and were recovered from the liver. The materials examined included orosomucoid, fetuin, ceruloplasmin, haptoglobin, agr2-macroglobulin, thyroglobulin, lactoferrin, and the two gonadotropic hormones, human chorionic gonadotropin and follicle-stimulating hormone.

Competitive inhibition of hepatic uptake was demonstrated by the injection of tracer amounts of 64Cu-ceruloplasmin together with substantive amounts of the above-mentioned desialylated proteins or the glycopeptides derived from them. Uptake was not inhibited by the fully sialylated protein or their glycopeptides.

Submitted on November 4, 1970


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