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Y Perrodon

Publications and source records attributed to Y Perrodon.

5 recordsLinked to original sources

Selection of BW 5147 subclones devoid of non-specific suppressive activity for use in cell hybridization.

Culture supernatants of BW 5147 cells widely used for T-cell hybridization often manifest non-MHC-restricted, non-antigen-specific regulatory activities on the mixed lymphocyte reaction (MLR) of mouse cells. This report demonstrates that, whereas supernatants of BW 5147 cells grown at low concentrations (2 X 10(5)/ml) enhanced MLR, high cell concentration (2 X 10(6)/ml) supernatants markedly inhibited this reaction. BW 5147 cell-free extracts significantly inhibited MLR and in vitro antibody production (PFC), as well as the mitogenic response to lipopolysaccharide E. coli (LPS) of mouse spleen cells, but did not affect the response to an optimal dose of phytohaemagglutinin (PHA). Both supernatant and cell-free extract inhibitory activities were located in 60,000 MW fraction. Inhibitory material of low MW (less than 12,000) was also found in high cell concentration supernatants. A similar suppressive activity was exerted by cell-free extracts of P3 X 63 NS cells used for B-cell hybridization. The suppressive activity seemed to stem from some kind of interaction between BW 5147 cells and the fetal calf serum (FCS) of the culture medium. Supernatants from subclones of BW 5147 cells obtained in selected batches of FCS and maintained in the same serum, even at high cell concentrations, did not affect MLR, whereas the supernatants from the same subclones maintained in other batches definitely suppressed this reaction. Thus, provided that culture conditions are chosen carefully, subclones of BW 5147 devoid of effect on in vitro immune reactions can be obtained.

Animals↗

Specification of the immune response: its suppression induced by chloramphenicol in vitro.

Specific in vitro PFC responses to trinitrophenyl conjugated to sheep red blood cells are inhibited by chloramphenicol (CAP), thiamphenicol (TAP), and diuron (DIU) by B-cell impairment. However, both mitogenic and polyclonal response to lipopolysaccharide is not affected by CAP and TAP but severely inhibited by DIU. Similarly, contact of cultured cells for the first 24 h with CAP did not much affect the 4th-day in vitro PFC response but the same incubation with DIU reduced it by 70%. Moreover, DIU used at the same concentration provoked an important mortality of cultured cells. These differences suggest that the target mechanism of CAP and TAP differs from that of DIU.

Animals↗

Separation and biological properties of Phaseolus vulgaris isolectins.

Two isolectins (L4E0-PHA and L0E4-PHA) from red kidney beans (Phaseolus vulgaris) were isolated by affinity chromatography on immobilized thyroglobulin and by chromatography on hydroxyapatite. The L4E0-PHA isolectin was not retarded on the affinity column and was eluted from the hydroxyapatite column with a 0.1 M Phosphate buffer. This isolectin had no erythroagglutinating activity but had high lymphoagglutinating and lymphocyte stimulating activities. The L0E4-PHA isolectin was adsorbed on the affinity column and was eluted from the hydroxyapatite column with a 0.25 M Phosphate buffer. This isolectin has a higo lymphocyte stimulating activity. These two isolectins are shown however to be closely related with respect to their oligomeric structure and reactivity towards anti-PHA antibodies. The lack of mitogenic activity of the L0E4-PHA isolectin suggests that in the other isolectins, the E monomer is not responsible for their mitogenic activity and that the membrane glycoproteins, which contain the E monomer - specific oligosaccharide, are not involved in the process inducing mitosis.

Agglutination↗

Limulin (Limulus polyphemus lectin): mitogenic effect on human peripheral lymphocytes.

The lectin from hemolymph of Limulus polyphemus was purified by affinity chromatography on insolubilized bovine submaxillary mucin. The purity of the protein was checked by crossed immunoelectrophoresis. Agglutination of human red blood cells was completely abolished after neuraminidase treatment, while other cells were still agglutinable after the same treatment but required a higher concentration of lectin. Limulin was able to simulate about 50% of human peripheral lymphocytes. This mitogenic effect could be inhibited by bovine submaxillary mucin but not by the disialylated mucin. Related to the known oligosaccharide-binding specificity of limulin and of the other nonspecific activators of lymphocytes, the authors suggest that lymphocyte stimulation is triggered by binding to a glyco-conjugate bearing the following carbohydrate chains: NANA leads to GalNac leads to or NANA leads to Gal leads to GlcNAc leads to Man.

Agglutinins↗