Regulatory effects of macrophage-secreted factors on T-lymphocyte colony growth

Sredni, B.; Michlin, H.; Kalechman, Y.; Rozenszajn, L.A.

Cellular Immunology 36(1): 15-27

1978


ISSN/ISBN: 0008-8749
PMID: 305288
DOI: 10.1016/0008-8749(78)90246-0
Accession: 068525768

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Abstract
Colonies of mouse T in liquid culture, were seeded in a 2-layer soft agar culture system containing the mitogen in the lower layer. The clonal proliferation was suppressed when culture fluid supernatants from macrophages (adherent peritoneal cells or spleen cells) from a number of mouse strains were incorporated in the agar culture system. The magnitude of the suppression was a function of the number of cells used to prepare the culture fluid and the amount of supernatant added to the culture. The inhibitory effect disappeared with dialysis and the dialyzed culture fluid exhibited an enhancing effect on T-lymphocyte colony proliferation. Diaflo ultrafiltration of culture fluid supernatant separated 2 substances; lymphocyte colony-inhibitory factor (LCIF), concentrated mainly in the fraction with MW of less than 1000; and lymphocyte colony-enhancing factor (LCEF), located chiefly in the fraction with MW of 10,000-30,000. The inhibitory factor was heat stable. The enhancing factor was heat sensitive. LCIF was not species specific. Adherent cells-macrophages release 2 biologic substances able to influence the cloning of T-lymphocytes, LCIF and LCEF. Unless the 2 are separated, the mild activity of LCEF is completely masked by the relatively strong action of LCIF.