Effect of Insulin on the Conversion of Glucose-C-14 to C-14-02 by Normal and Diabetic Fibroblasts in Culture

In an attempt to elucidate the basic genetic defect (s) in diabetes, the acute effect of insulin on the conversion of glucose-C-14 to C-14-02 in cultured human diploid fibroblasts was measured under various conditions. Freshly trypsinized cells did not respond to insulin, but after more than sixteen hours in growth medium, a small but significant stimulation, requiring high concentrations of insulin (0.26 U. per ml.) was observed. Stimulation by insulin in various normal strains ranged from 5 to 45 per cent with a mean of 18 per cent (p < .001). C-14-O2 production was approximately linear with time after an initial lag phase and proportional to the number of cells inoculated. Increasing the concentration of glucose in the medium increased C-14-O2 production, with stimulation by insulin apparent at only very low concentrations and at 250 mg. per 100 ml., the highest concentration studied. Experiments comparing the oxidation of glucose-l-C-14 versus glucose-6-C-14 showed that substantial C-14-O2 production occurred via the hexose monophosphate shunt, but that most of the increase in C-14-O2 production in the presence of insulin occurred via the Krebs cycle. A comparison of basal and insulin-stimulated C-14-O2 production in normal and diabetic fibroblasts revealed no significant differences. Possible explanations for the failure to distinguish between the two groups are discussed.

[1]  H. Amos,et al.  Insulin Dependence of Cells in Primary Culture: Influence on Ribosome Integrity , 1968, Nature.

[2]  M. Rodbell Metabolism of isolated fat cells. V. Preparation of "ghosts" and their properties; adenyl cyclase and other enzymes. , 1967, The Journal of biological chemistry.

[3]  M. Rodbell Metabolism of isolated fat cells. VI. The effects of insulin, lipolytic hormones, and theophylline on glucose transport and metabolism in "ghosts". , 1967, The Journal of biological chemistry.

[4]  Y. J. Topper,et al.  Hormone-Dependent Differentiation of Immature Mouse Mammary Gland in vitro , 1967, Science.

[5]  J. Kuo,et al.  Comparison of the effects of Bacillus subtilis protease, type 8 (subtilopeptidase A), and insulin on isolated adipose cells. , 1967, The Journal of biological chemistry.

[6]  F. Stockdale,et al.  Insulin-dependent DNA polymerase and DNA synthesis in mammary epithelial cells in vitro. , 1967, Proceedings of the National Academy of Sciences of the United States of America.

[7]  R. W. Turkington,et al.  Androgen inhibition of mammary gland differentiation in vitro. , 1967, Endocrinology.

[8]  F. Stockdale,et al.  The role of DNA synthesis and mitosis in hormone-dependent differentiation. , 1966, Proceedings of the National Academy of Sciences of the United States of America.

[9]  H. Katzen The effect of diabetes and insulin in vivo and in vitro on a low Km form of hexokinase from various rat tissues. , 1966, Biochemical and biophysical research communications.

[10]  H. Kalter Genetics and the Epidemiology of Chronic Diseases. , 1966 .

[11]  J. Gliemann Insulin-like Activity of Dilute Human Serum Assayed by an Isolated Adipose Cell Method , 1965, Diabetes.

[12]  R. Schimke,et al.  Multiple forms of hexokinase in the rat: tissue distribution, age dependency, and properties. , 1965, Proceedings of the National Academy of Sciences of the United States of America.

[13]  R. Levine Cell membrane as a primary site of insulin action. , 1965, Federation proceedings.

[14]  H. Nitowsky,et al.  KINETIC AND ELECTROPHORETIC EVIDENCE FOR MULTIPLE FORMS OF GLUCOSE-ATP PHOSPHOTRANSFERASE ACTIVITY FROM HUMAN CELL CULTURES AND RAT LIVER. , 1965, Biochemical and biophysical research communications.

[15]  L. Hayflick THE LIMITED IN VITRO LIFETIME OF HUMAN DIPLOID CELL STRAINS. , 1965, Experimental cell research.

[16]  P. Rieser,et al.  Anabolic Responses of Diaphragm Muscle to Insulin and to Other Pancreatic Proteins.∗ , 1964, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[17]  M. Rodbell METABOLISM OF ISOLATED FAT CELLS. I. EFFECTS OF HORMONES ON GLUCOSE METABOLISM AND LIPOLYSIS. , 1964, The Journal of biological chemistry.

[18]  J. Paul,et al.  A comparative study of respiratory metabolism in cultured mammalian cell strains. , 1963, Experimental cell research.

[19]  I. Mirsky,et al.  Action of oxytocin and related peptides on epididymal adipose tissue of the rat. , 1962, Endocrinology.

[20]  J. Paul,et al.  Environmental factors influencing respiration of strain L cells. , 1961, Experimental cell research.

[21]  P. Ove,et al.  Growth factors for mammalian cells in culture. , 1959, The Journal of biological chemistry.

[22]  E. Ball,et al.  Studies on the metabolism of adipose tissue. I. The effect of insulin on glucose utilization as measured by the manometric determination of carbon dioxide output. , 1959, The Journal of biological chemistry.

[23]  A. Renold,et al.  Studies on rat adipose tissue in vitro. II. Effects of insulin on the metabolism of specifically labeled glucose. , 1958, The Journal of biological chemistry.

[24]  E. F. Davidenkova,et al.  [Genetics of diabetes mellitus]. , 1970, Vestnik Akademii meditsinskikh nauk SSSR.

[25]  A. Sols,et al.  Induced biosynthesis of liver glucokinase. , 1964, Advances in enzyme regulation.

[26]  C. Park,et al.  The regulation of glucose uptake in muscle as studied in the perfused rat heart. , 1961, Recent progress in hormone research.

[27]  I. Leslie,et al.  The metabolism of human embryonic and malignant cells and their response to insulin. , 1957, Biochimica et biophysica acta.