in vivo Ageing of human erythrocytes and cell-surface labeling by metaperiodate and sodium borotritide.

Young and old human erythrocytes, separated in vitro according to age, were labeled at the surface-sialic acid residues by sodium periodate and borotritide treatment. No qualitative difference was observed between the sialic acid derivatives of young- and old-erythrocyte membranes. The number of labeled residues was significantly decreased in the in vivo aged erythrocytes (12 +/- 2.

Red cell ageing: phagocytosis and life-span of young and old erythrocytes fractionated by centrifugation.

Young and old red blood cells, separated by centrifugation on the basis of differences in cell density, were submitted to phagocytosis by either autologous human alveolar macrophages or syngeneic murine bone-marrow macrophages. Young cells adhere to macrophages, but to a much smaller extent than old ones. The influence of both type and quality of the separation procedure on the differences observed between the two erythrocyte subpopulations is discussed in the light of the half-life times of murine young and old red blood cells.

A glucose-containing fraction extracted from the young erythrocyte membrane is capable of transferring glucose to hemoglobin in vitro.

Red blood cell (RBC) membranes are rich in a glycoconjugate that is extractable in chloroform/methanol solutions (2/1, v/v) and contains several hexoses, such as glucose. Old and young RBC are separated and their respective glycoconjugates are prepared. HbA0 is purified by column chromatography and incubated with solutions of this conjugate.

Receptors for peanut agglutinin in lymphocytes from patients with cirrhosis of the liver.

A population of peripheral blood lymphocytes exhibits specific receptor for the peanut lectin (Arachis hypogaea). In control subjects, this population represents 1.3% of all lymphocytes while it represents 13% in patients with alcoholic cirrhosis.

Design and feasibility of a flexible computerized system for the clinical laboratory, based on the IEEE 488 standardized interface.

Our target is to build a flexible computerized system based on an informational study of the clinical laboratory, which would leave the laboratory staff free to use equipment or modules from different manufacturers interchangeably. This applies to hardware and software. To fulfil this objective, it is necessary that automatic analyzers, microcomputers and minicomputers, have built-in standardized hardware and software interfaces.