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. 1984 Oct 1;223(1):39–46. doi: 10.1042/bj2230039

Insulin-responsive cultured foetal-rat hepatocytes. Their preparation and characterization.

D C DeSante, L Little, D E Peavy, F Vinicor
PMCID: PMC1144261  PMID: 6388565

Abstract

An improved non-perfusion method for the preparation of cultured foetal-rat hepatocytes is described. Digestion of the liver with collagenase and deoxyribonuclease I gave yields of 40 X 10(6) hepatocytes/g of liver. The plating efficiency of hepatocytes in medium with 10 microM-cortisol was 50%. Cell morphology and metabolism were maintained through 3 days of monolayer culture, with minimal contamination by haematopoietic cells or fibroblasts. The cultured cells bound and degraded 125I-insulin in a time- and dose-dependent manner. The estimated ED50 for competitive binding at 37 degrees C was 1.1 nM. Curvilinear Scatchard plots were observed, with estimates of 16 500 high-affinity sites (Kd = 813 pM) and 53 000 low-affinity sites (Kd = 23 nM) per cell. The cultured cells demonstrated a glycogenic response to insulin, with an estimated ED50 of 120 pM. The degree of glycogenic response to insulin varied with time in culture: 500% above basal on day 1, 200% on day 2, and only 150% on day 3. Cultured foetal cells also exhibited a time-dependent uptake of 2-aminoisobutyric acid, which, in contrast with previous reports with adult cells, was not stimulated by the presence of 10 nM-insulin. Cultured foetal hepatocytes may provide an interesting model with which to study the relationship between insulin-receptor binding and insulin action.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Armato U., Draghi E., Andreis P. G. Effect of glucagon and insulin on the growth of neonatal rat hepatocytes in primary tissue culture. Endocrinology. 1978 Apr;102(4):1155–1166. doi: 10.1210/endo-102-4-1155. [DOI] [PubMed] [Google Scholar]
  2. Autuori F., Baldini P., Luzzatto A. C., Devirgiliis L. C., Dini L., Incerpi S., Luly P. Insulin binding and internalization in rat hepatocytes during prenatal and postnatal life. Biochim Biophys Acta. 1981 Nov 18;678(1):1–6. doi: 10.1016/0304-4165(81)90040-4. [DOI] [PubMed] [Google Scholar]
  3. Baur H., Kasperek S., Pfaff E. Criteria of viability of isolated liver cells. Hoppe Seylers Z Physiol Chem. 1975 Jun;356(6):827–838. doi: 10.1515/bchm2.1975.356.s1.827. [DOI] [PubMed] [Google Scholar]
  4. Bellemann P., Gebhardt R., Mecke D. An improved method for the isolation of hepatocytes from liver slices. Selective removal of Trypan blue-dyeable cells. Anal Biochem. 1977 Aug;81(2):408–415. doi: 10.1016/0003-2697(77)90711-4. [DOI] [PubMed] [Google Scholar]
  5. Blackard W. G., Nelson N. C. Portal and peripheral vein immunoreactive insulin concentrations before and after glucose infusion. Diabetes. 1970 May;19(5):302–306. doi: 10.2337/diab.19.5.302. [DOI] [PubMed] [Google Scholar]
  6. Blazquez E., Rubalcava B., Montesano R., Orci L., Unger R. H. Development of insulin and glucagon binding and the adenylate cyclase response in liver membranes of the prenatal, postnatal, and adult rat: evidence of glucagon "resistance". Endocrinology. 1976 Apr;98(4):1014–1023. doi: 10.1210/endo-98-4-1014. [DOI] [PubMed] [Google Scholar]
  7. Bourbon J., Gilbert M. Role of fetal insulin in glycogen metabolism in the liver of the rat fetus. Biol Neonate. 1981;40(1-2):38–45. doi: 10.1159/000241470. [DOI] [PubMed] [Google Scholar]
  8. Cesarone C. F., Bolognesi C., Santi L. Improved microfluorometric DNA determination in biological material using 33258 Hoechst. Anal Biochem. 1979 Nov 15;100(1):188–197. doi: 10.1016/0003-2697(79)90131-3. [DOI] [PubMed] [Google Scholar]
  9. DeLean A., Munson P. J., Rodbard D. Simultaneous analysis of families of sigmoidal curves: application to bioassay, radioligand assay, and physiological dose-response curves. Am J Physiol. 1978 Aug;235(2):E97–102. doi: 10.1152/ajpendo.1978.235.2.E97. [DOI] [PubMed] [Google Scholar]
  10. Devirgiliis L. C., Dini L., Di Pierro A., Leoni S., Spagnuolo S., Stefanini S. An improved non-perfusion method for the isolation and purification of rat foetal and neonatal hepatocytes. Cell Mol Biol Incl Cyto Enzymol. 1981;27(6):687–694. [PubMed] [Google Scholar]
  11. Draznin B., Trowbridge M. Inhibition of intracellular proteolysis by insulin in isolated rat hepatocytes. Possible role of internalized hormone. J Biol Chem. 1982 Oct 25;257(20):11988–11993. [PubMed] [Google Scholar]
  12. Feldman H. A. Mathematical theory of complex ligand-binding systems of equilibrium: some methods for parameter fitting. Anal Biochem. 1972 Aug;48(2):317–338. doi: 10.1016/0003-2697(72)90084-x. [DOI] [PubMed] [Google Scholar]
  13. Felix J. M., Sutter-Dub M. T., Legrele C. Studies on the different forms of material reacting with antiinsulin antibodies in the fetal and adult rat. Horm Metab Res. 1975 Sep;7(5):394–399. doi: 10.1055/s-0028-1093735. [DOI] [PubMed] [Google Scholar]
  14. Fricke R., Clark C. M., Jr Augmentation of glucose and amino acid uptake by insulin in the developing rat diaphragm. Am J Physiol. 1973 Jan;224(1):117–121. doi: 10.1152/ajplegacy.1973.224.1.117. [DOI] [PubMed] [Google Scholar]
  15. GOA J. A micro biuret method for protein determination; determination of total protein in cerebrospinal fluid. Scand J Clin Lab Invest. 1953;5(3):218–222. doi: 10.3109/00365515309094189. [DOI] [PubMed] [Google Scholar]
  16. Girard J. R., Cuendet G. S., Marliss E. B., Kervran A., Rieutort M., Assan R. Fuels, hormones, and liver metabolism at term and during the early postnatal period in the rat. J Clin Invest. 1973 Dec;52(12):3190–3200. doi: 10.1172/JCI107519. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Glinsmann W. H., Eisen H. J., Lynch A., Chez R. A. Glucose regulation by isolated near term fetal monkey liver. Pediatr Res. 1975 Jul;9(7):600–604. doi: 10.1203/00006450-197507000-00009. [DOI] [PubMed] [Google Scholar]
  18. Greengard O., Federman M., Knox W. E. Cytomorphometry of developing rat liver and its application to enzymic differentiation. J Cell Biol. 1972 Feb;52(2):261–272. doi: 10.1083/jcb.52.2.261. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Guidotti G. G., Borghetti A. F., Gazzola G. C. The regulation of amino acid transport in animal cells. Biochim Biophys Acta. 1978 Dec 15;515(4):329–366. doi: 10.1016/0304-4157(78)90009-6. [DOI] [PubMed] [Google Scholar]
  20. Handlogten M. E., Kilberg M. S. Transport system a is not responsive to hormonal stimulation in primary cultures of fetal rat hepatocytes. Biochem Biophys Res Commun. 1982 Oct 15;108(3):1113–1119. doi: 10.1016/0006-291x(82)92115-5. [DOI] [PubMed] [Google Scholar]
  21. Hay W. W., Jr Fetal glucose metabolism. Semin Perinatol. 1979 Apr;3(2):157–176. [PubMed] [Google Scholar]
  22. Kelly P. A., Posner B. I., Tsushima T., Friesen H. G. Studies of insulin, growth hormone and prolactin binding: ontogenesis, effects of sex and pregnancy. Endocrinology. 1974 Aug;95(2):532–539. doi: 10.1210/endo-95-2-532. [DOI] [PubMed] [Google Scholar]
  23. Kilberg M. S. Amino acid transport in isolated rat hepatocytes. J Membr Biol. 1982;69(1):1–12. doi: 10.1007/BF01871236. [DOI] [PubMed] [Google Scholar]
  24. LEIBOVITZ A. THE GROWTH AND MAINTENANCE OF TISSUE-CELL CULTURES IN FREE GAS EXCHANGE WITH THE ATMOSPHERE. Am J Hyg. 1963 Sep;78:173–180. doi: 10.1093/oxfordjournals.aje.a120336. [DOI] [PubMed] [Google Scholar]
  25. Laishes B. A., Williams G. M. Conditions affecting primary cell cultures of functional adult rat hepatocytes. 1. The effect of insulin. In Vitro. 1976 Jul;12(7):521–532. doi: 10.1007/BF02796495. [DOI] [PubMed] [Google Scholar]
  26. Laishes B. A., Williams G. M. Conditions affecting primary cell cultures of functional adult rat hepatocytes. II. Dexamethasone enhanced longevity and maintenance of morphology. In Vitro. 1976 Dec;12(12):821–832. doi: 10.1007/BF02796367. [DOI] [PubMed] [Google Scholar]
  27. Leffert H. L., Paul D. Studies on primary cultures of differentiated fetal liver cells. J Cell Biol. 1972 Mar;52(3):559–568. doi: 10.1083/jcb.52.3.559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Marceau N., Goyette R., Valet J. P., Deschenes J. The effect of dexamethasone on formation of a fibronectin extracellular matrix by rat hepatocytes in vitro. Exp Cell Res. 1980 Feb;125(2):497–502. doi: 10.1016/0014-4827(80)90146-9. [DOI] [PubMed] [Google Scholar]
  29. Marceau N., Noël M., Deschênes J. Growth and functional activities of neonatal and adult rat hepatocytes cultured on fibronectin coated substratum in serum-free medium. In Vitro. 1982 Jan;18(1):1–11. doi: 10.1007/BF02796379. [DOI] [PubMed] [Google Scholar]
  30. McCormick K. L., Susa J. B., Widness J. A., Singer D. B., Adamsons K., Schwartz R. Chronic hyperinsulinemia in the fetal rhesus monkey: effects on hepatic enzymes active in lipogenesis and carbohydrate metabolism. Diabetes. 1979 Dec;28(12):1064–1068. doi: 10.2337/diab.28.12.1064. [DOI] [PubMed] [Google Scholar]
  31. Menuelle P., Plas C. Relationship between insulin binding and glycogenesis in cultured fetal hepatocytes. Diabetologia. 1981 Jun;20(6):647–653. doi: 10.1007/BF00257435. [DOI] [PubMed] [Google Scholar]
  32. Munson P. J., Rodbard D. Ligand: a versatile computerized approach for characterization of ligand-binding systems. Anal Biochem. 1980 Sep 1;107(1):220–239. doi: 10.1016/0003-2697(80)90515-1. [DOI] [PubMed] [Google Scholar]
  33. Murison G. L. Growth of fetal rat liver cells in response to hydrocortisone. Exp Cell Res. 1976 Jul;100(2):439–443. doi: 10.1016/0014-4827(76)90177-4. [DOI] [PubMed] [Google Scholar]
  34. Neufeld N. D., Scott M., Kaplan S. A. Ontogeny of the mammalian insulin receptor. Studies of human and rat fetal liver plasma membranes. Dev Biol. 1980 Jul;78(1):151–160. doi: 10.1016/0012-1606(80)90325-5. [DOI] [PubMed] [Google Scholar]
  35. Noyes W. F. Culture of human fetal liver. Proc Soc Exp Biol Med. 1973 Oct 1;144(1):245–248. doi: 10.3181/00379727-144-37565. [DOI] [PubMed] [Google Scholar]
  36. Peavy D. E., Edmondson J. W., Duckworth W. C. Selective effects of inhibitors of hormone processing on insulin action in isolated hepatocytes. Endocrinology. 1984 Mar;114(3):753–760. doi: 10.1210/endo-114-3-753. [DOI] [PubMed] [Google Scholar]
  37. Plas C., Chapeville F., Jacquot R. Development of glycogen storage ability under cortisol control in primary cultures of rat fetal hepatocytes. Dev Biol. 1973 May;32(1):82–91. doi: 10.1016/0012-1606(73)90221-2. [DOI] [PubMed] [Google Scholar]
  38. Plas C., Desbuquois B. Receptor-mediated insulin degradation and insulin-stimulated glycogenesis in cultured foetal hepatocytes. Biochem J. 1982 Feb 15;202(2):333–341. doi: 10.1042/bj2020333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Plas C., Nunez J. Role of cortisol on the glycogenolytic effect of glucagon and on the glycogenic response to insulin in fetal hepatocyte culture. J Biol Chem. 1976 Mar 10;251(5):1431–1437. [PubMed] [Google Scholar]
  40. Plas C. Recherches sur la différenciation fonctionnelle chez le foetus de rat. Séparation et culture des hépatocytes à partir d'une suspension cellulaire. C R Acad Sci Hebd Seances Acad Sci D. 1969 Jan 6;268(1):143–146. [PubMed] [Google Scholar]
  41. Salhanick A. I., Krupp M. N., Amatruda J. M. Dexamethasone stimulates insulin receptor synthesis in cultured rat hepatocytes. J Biol Chem. 1983 Dec 10;258(23):14130–14135. [PubMed] [Google Scholar]
  42. Sara V. R., Hall K., Misaki M., Fryklund L., Christensen N., Wetterberg L. Ontogenesis of somatomedin and insulin receptors in the human fetus. J Clin Invest. 1983 May;71(5):1084–1094. doi: 10.1172/JCI110858. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Van Handel E. Estimation of glycogen in small amounts of tissue. Anal Biochem. 1965 May;11(2):256–265. doi: 10.1016/0003-2697(65)90013-8. [DOI] [PubMed] [Google Scholar]
  44. Vinicor F., Higdon G., Clark J. F., Clark C. M., Jr Development of glucagon sensitivity in neonatal rat liver. J Clin Invest. 1976 Sep;58(3):571–578. doi: 10.1172/JCI108503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Vinicor F., Kiedrowski L. Characterization of the hepatic receptor for insulin in the perinatal rat. Endocrinology. 1982 Mar;110(3):782–790. doi: 10.1210/endo-110-3-782. [DOI] [PubMed] [Google Scholar]
  46. Watts C., Gain K. R. Insulin in the rat fetus. A new form of circulating insulin. Diabetes. 1984 Jan;33(1):50–56. doi: 10.2337/diab.33.1.50. [DOI] [PubMed] [Google Scholar]
  47. Williams G. M., Bermudez E., San R. H., Goldblatt P. J., Laspia M. F. Rat hepatocyte primary cultures. IV. Maintenance in defined medium and the role of production of plasminogen activator and other proteases. In Vitro. 1978 Oct;14(10):824–837. doi: 10.1007/BF02616152. [DOI] [PubMed] [Google Scholar]
  48. de Meyts P., Roth J., Neville D. M., Jr, Gavin J. R., 3rd, Lesniak M. A. Insulin interactions with its receptors: experimental evidence for negative cooperativity. Biochem Biophys Res Commun. 1973 Nov 1;55(1):154–161. doi: 10.1016/s0006-291x(73)80072-5. [DOI] [PubMed] [Google Scholar]

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