Affiliation:
1. Laboratory of the Comparative Biochemistry of Enzymes, Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, Saint-Petersburg, Russian Federation
2. Department of Molecular Medicine and Byrd Alzheimer's Research Institute, Morsani College of Medicine, University of South Florida, Tampa, Florida 33612, United States
Abstract
Insulin internalization and processing of the Insulin Receptor Complex (IRC) inside the cell are
important components of the intracellular Mechanism of Insulin Action (MIA). They define the continuation
of intracellular signaling of IRC and allow utilization of the parts of the complex after ligand dissociation.
Traditionally, changes in the insulin regulatory system associated with the vertebrate phylogenesis have
been evaluated by changes of its two elements: the hormone and its receptor. A hormone-competent cell was
considered as an evolutionarily completed element of insulin regulatory system. However, previous studies
of the isolated hepatocytes of four classes of vertebrates (lamprey, frog, chicken, and rat) revealed significant
differences in the state of internalization of 125I-insulin and intracellular IRC processing. Radical differences
were noted in the regulation of 125I-insulin internalization and the intracellular fate of the IRC. Here,
cytosolic efficient insulin degradation and a complete lack of 125I-insulin exocytosis were observed in the
cyclostome cells, whereas in amphibians the hormone underwent lysosomal degradation and showed low
levels of exocytosis, while birds and mammals were characterized by high volumes of the excreted 125Iinsulin
containing proteolytic 125I-insulin fragments. Despite the established recognition of the importance
of the temperature factor, a complete understanding of the molecular mechanisms underlying the temperature
effects on MIA is still missing. This poorly studied problem of the MIA temperature dependence can be
behind the differences in the effect of temperature on the intracellular action of insulin and IGF-I. In fact, at
different phylogenetic stages, successive changes were reported for the temperature dependence of the 125Iinsulin
internalization and exocytosis. The following regularities were reported for the effect of temperature
on the 125I-insulin internalization in isolated hepatocytes of different origin: complete lack of receptibility of
the process to temperature in lampreys, receptibility of the process in a narrow range of low temperatures
(0-5°C) in amphibians, and flexible regulation of 125I-insulin internalization in a wide temperature range (6-
37°C) in the cells from endothermic organisms. Reported data make it possible to observe three stages in the
alteration of temperature regulation of 125I-insulin internalization (in cells of cyclostomes, amphibians, and
endothermic organisms) and two stages of temperature regulation of 125I-insulin exocytosis in cells of amphibians,
birds, and mammals. The data presented in this study reflect the specificity of the developmental
reorganization of the intracellular MIA regulation and hormone utilization, and emphasize the central role of
temperature in selective MIA formation during vertebrate phylogenesis.
Funder
Russian Academy of Sciences
State Oder
Publisher
Bentham Science Publishers Ltd.
Subject
Cell Biology,Molecular Biology,Biochemistry,General Medicine
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