TY - JOUR
T1 - An inhibitor of cell proliferation released by cultures of macrophages
AU - Calderon, J.
AU - Williams, R. T.
AU - Unanue, E. R.
PY - 1974
Y1 - 1974
N2 - Culture fluids from mouse peritoneal exudate cells inhibited [3H]thymidine incorporation by, and proliferation of, EL 4 leukemia cells, 3T3 cells, and mitogen stimulated spleen lymphocytes. Inhibited EL 4 leukemia cells recovered their normal proliferative capacity when washed and incubated in normal medium. The inhibitory activity resided in a low mol wt substance that could be absorbed by incubation with the tumor cells. This substance was dialyzable and resistant to tryptic digestion and phosphodiesterase treatment. The mononuclear phagocytes in the peritoneal exudate seemed to be the source of the inhibitor. The inhibitory material was found in the same amounts in exudates of normal mice or mice injected with peptone or infected with Listeria monocytogenes; spleen cells adherent to plastic released the inhibitor but in lesser amount. It is suggested that this inhibitor may contribute to the deleterious effects found when various cells, including neoplastic ones, are cultured in the presence of macrophages.
AB - Culture fluids from mouse peritoneal exudate cells inhibited [3H]thymidine incorporation by, and proliferation of, EL 4 leukemia cells, 3T3 cells, and mitogen stimulated spleen lymphocytes. Inhibited EL 4 leukemia cells recovered their normal proliferative capacity when washed and incubated in normal medium. The inhibitory activity resided in a low mol wt substance that could be absorbed by incubation with the tumor cells. This substance was dialyzable and resistant to tryptic digestion and phosphodiesterase treatment. The mononuclear phagocytes in the peritoneal exudate seemed to be the source of the inhibitor. The inhibitory material was found in the same amounts in exudates of normal mice or mice injected with peptone or infected with Listeria monocytogenes; spleen cells adherent to plastic released the inhibitor but in lesser amount. It is suggested that this inhibitor may contribute to the deleterious effects found when various cells, including neoplastic ones, are cultured in the presence of macrophages.
UR - http://www.scopus.com/inward/record.url?scp=0016276606&partnerID=8YFLogxK
U2 - 10.1073/pnas.71.11.4273
DO - 10.1073/pnas.71.11.4273
M3 - Article
C2 - 4216017
AN - SCOPUS:0016276606
SN - 0027-8424
VL - 71
SP - 4273
EP - 4277
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 11
ER -