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Title: Multiple hormonal control of enzyme synthesis in liver and hepatoma cells

Technical Report ·
DOI:https://doi.org/10.2172/5652696· OSTI ID:5652696

Synthesis of hepatic tyrosine aminotransferase is accelerated in vivo by either of the pancreatic hormones, insulin and glucagon as well as by glucocorticoids, and glucagon acts via the intracellular mediator, cyclic AMP. The mechanisms responsive to these hormones have also been retained in cultured hepatoma cells: in H-35 cells the responses appear to be essentially identical to those in liver, especially in that each inducer can act independently of the others. In this paper we describe recent analyses of the cellular mechanisms involved in this multiple hormonal control of synthesis of a single enzyme. These experiments have been done with rat liver in vivo, owing to a need for larger quantities of cellular components that can readily be obtained from cultured cells. As some of these results appear to be at variance in important respects with those of earlier analyses carried out in H-35 cells, we briefly review these earlier experiments as well.

Research Organization:
Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Tennessee Univ., Oak Ridge (USA). Graduate School of Biomedical Sciences
DOE Contract Number:
W-7405-ENG-26
OSTI ID:
5652696
Report Number(s):
CONF-780862-1
Resource Relation:
Conference: Symposium on hormones and cell culture, Cold Spring Harbor, NY, USA, 29 Aug 1978
Country of Publication:
United States
Language:
English