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C Sumida

Publications and source records attributed to C Sumida.

56 records · Page 4Linked to original sources

Fatty acids: ancestral ligands and modern co-regulators of the steroid hormone receptor cell signalling pathway.

Long chain fatty acids derived from endogenous metabolism and/or nutrition are regulators of cell signalling pathways. They can be lipid second messengers of signal transduction systems or modulators and regulators of intracellular signalling pathways such as those involved in the mechanism of action of steroid hormones. Fatty acids have been shown to activate gene transcription under the control of some evolutionarily primitive members of the steroid/thyroid superfamily of receptors. They may represent ancestral ligands of this superfamily of receptors. Fatty acids are also known to regulate the activity of protein kinases, particularly protein kinase C, and thereby phosphorylation of intracellular proteins involved in regulation of gene transcription. Fatty acids may be co-regulators in the cross-talk between membrane-triggered signal transduction and the intracellular steroid hormone signalling pathway. Fatty acids are known to affect either negatively and/or positively the binding of steroid hormones to their specific plasma transport proteins and their specific intracellular receptors and, very recently, fatty acids have also been shown to co-regulate glucocorticoid-dependent gene expression. The mechanism of action of steroid hormones will be used as an illustration of how fatty acids can intervene at different levels of cellular organization to regulate biological activity, with a focus on the glucocorticoid receptor.

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[Oestradiol receptors in foetal compartment (author's transl)].

Oestradiol concentration in the foetal plasma of guinea pig is 160-200 pg/ml (20-35 days of gestation), 200-300 pg/ml (35-45 days of gestation) and 170-450 pg/ml (45-60 days of gestation). After 3H-oestradiol administration to the foetus, this hormone circulates mainly as non-transformed 3H-oestradiol, 3H-oestrone and 3H-oestrone sulphate. 97-99% of the circulating oestradiol is found in unbound form. In vivo and in vitro studies in the foetus of guinea pig (40-55 days of gestation) show the presence of specific oestradiol receptors in the kidney, brain and Mullerian ducts of the foetus. The affinity constant in the cytosol of the brain is Kd=2 X 10(=9)M; in the cytosol kidney this value is Kd = 2.3 X 10(=10)M. A direct binding of 3H-oestradiol to the chromatin of the kidney was demonstrated with a Kd = 3.3 X 10(=10)M In the cytosol of Mullerian ducts the presence of a specific 3H-oestradiol macromolecule component with a sedimentation coefficient (in sucrose gradient) of 8-8.5S was detected. It is concluded that specific oestradiol receptors are present during foetal development in tissues such as kidney, brain and Mullerian ducts, but not in the liver.

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