At low concentrations (i.e., 10(-12)-10(-9) mol/1), PGF1 alpha and PGF2 alpha very intensely stimulated both the DNA-synthetic and mitotic activities of hepatocytes in 4-day-old primary cultures of neonatal rat liver. DNA replication was more intensely enhanced by PGF2 alpha than by PGF1 alpha, whereas mitotic activity was nearly equally affected by the two prostaglandins. On the whole, the growth-promoting activity of PGF1 alpha used by itself or in equimolar mixtures with other prostaglandins (e.g., A1, E1, etc.) mimicked that of arachidonic acid we previously reported (1). On a molar basis, PGF2 alpha by itself stimulated hepatocytes' DNA synthesis more powerfully than arachidonate did, and when used in equimolar mixtures with other prostaglandins was at least as potent as arachidonic acid. These observations establish prostaglandins of the F series as quite powerful commitment factors and, though by a lesser degree, also intracycle regulators for neonatal rat hepatocytes in primary culture. However, the understanding of the role(s) of prostaglandins of F and other series in the physiological control of hepatocytes' proliferative activation must await the clarification of their interaction(s) with other arachidonate derivative(s) and polypeptide growth factor(s) which also may be involved in the process.

Prostaglandins of the F series are extremely powerful growth factors for primary neonatal rat hepatocytes.

ARMATO, Ubaldo;
1983-01-01

Abstract

At low concentrations (i.e., 10(-12)-10(-9) mol/1), PGF1 alpha and PGF2 alpha very intensely stimulated both the DNA-synthetic and mitotic activities of hepatocytes in 4-day-old primary cultures of neonatal rat liver. DNA replication was more intensely enhanced by PGF2 alpha than by PGF1 alpha, whereas mitotic activity was nearly equally affected by the two prostaglandins. On the whole, the growth-promoting activity of PGF1 alpha used by itself or in equimolar mixtures with other prostaglandins (e.g., A1, E1, etc.) mimicked that of arachidonic acid we previously reported (1). On a molar basis, PGF2 alpha by itself stimulated hepatocytes' DNA synthesis more powerfully than arachidonate did, and when used in equimolar mixtures with other prostaglandins was at least as potent as arachidonic acid. These observations establish prostaglandins of the F series as quite powerful commitment factors and, though by a lesser degree, also intracycle regulators for neonatal rat hepatocytes in primary culture. However, the understanding of the role(s) of prostaglandins of F and other series in the physiological control of hepatocytes' proliferative activation must await the clarification of their interaction(s) with other arachidonate derivative(s) and polypeptide growth factor(s) which also may be involved in the process.
1983
F prostaglandins; proliferation; primary neonatal rat hepatocytes
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/233789
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