Premium
Specific binding and biological effects of tumor promoting phorbol esters on sponges
Author(s) -
Mazzorana M.,
Garrone R.,
Martel N.,
Yamasaki H.
Publication year - 1985
Publication title -
biology of the cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 85
eISSN - 1768-322X
pISSN - 0248-4900
DOI - 10.1111/j.1768-322x.1985.tb00322.x
Subject(s) - biology , potency , phorbol , receptor , binding site , biochemistry , biological activity , phorbol ester , sponge , in vitro , protein kinase c , microbiology and biotechnology , enzyme , botany
Sponges grown in the presence of 12‐O‐tetradecanoyl phorbol‐13‐acetate (TPA) show deep alterations of their structure and development. Their aquiferous system (flagellated cells and canals) is largely altered and the tissues show an unusually high cell density. This focalized effect of TPA on the aquiferous system seems specific and is reversible at low concentrations (100 ng/ml). A toxic, non‐specific effect is also noted, particularly at high concentrations (5000 ng/ml). Using 3H‐phorbol‐12, 13‐dibutyrate (3H‐PDBu), we demonstrate a class of specific binding sites for phorbol esters in the homogenates of sponges. These binding sites have high affinity (Kd = 26.0 nM) for PDBu and at saturation about 20 pmoles of 3H‐PDBu is bound per mg protein of sponge homogenates. The binding of 3H‐PDBu was inhibited by other phorbol esters and their congeners, and there was a good correlation between their potency in binding inhibition and their tumor promoting activity. It is concluded that sponges have a class of specific saturable and high affinity receptors for phorbol esters and that there is a very high conservation of these receptors during evolution. Such specific binding may be responsible for subsequent biological effect of TPA on sponges.