Paracrine interaction between hepatocytes and macrophages after extrathyroidal proteolysis of thyroglobulin

Thyroglobulin (Tg), the precursor of the thyroid hormones triiodothyronine (T3) and thyroxine (T4), is known to derive from thyroid epithelial cells. Part of Tg reaches the circulation as an intact molecule by transcytosis across the epithelial wall of thyroid follicles. Circulating Tg is a potential ligand for the asialoglycoprotein receptor of hepatocytes. In this report we show, however, that clearance of circulating Tg occurred exclusively by endocytosis in liver macrophages, whereas hepatocytes did not participate in this process. The biological significance of this Tg uptake by the macrophages might consist in an increase of thyroid hormones in close proximity to the macrophages, thereby affecting the hepatocyte metabolism. To test this hypothesis, co‐cultures of hepatocytes and macrophages were incubated with Tg, which resulted in the release of thyroid hormones and in a significant increase in the activity of lipogenesis and of hepatocellular key enzymes of the hexose monophosphate shunt. This effect of Tg could be mimicked by equivalent amounts of T3 or T4 exclusively in the co‐cultures. When hepatocytes were incubated with thyroid hormones in the absence of macrophages, no or only little effect was observed, indicating that the interaction of macrophages and hepatocytes was a prerequisite for the stimulation of the hepatocellular metabolism. We conclude that the paracrine effect on HepG2 cells results from the degradation of Tg in J774 cells. Apparently, this process is not confined to the release of thyroid hormones, but it requires the interaction of both cell types, possibly mediated by an additional, as yet unknown stimulus.

[1]  G. Ramadori,et al.  Synthesis of insulinlike growth factor binding proteins and of the acid‐labile subunit in primary cultures of rat hepatocytes, of Kupffer cells, and in cocultures: Regulation by insulin, insulinlike growth factor, and growth hormone , 1996, Hepatology.

[2]  S. Mustafa,et al.  Endothelin association with the cultured rat Kupffer cell: Characterization and regulation , 1995, Hepatology.

[3]  T. Billiar,et al.  The role of nitric oxide in Kupffer cell-hepatocyte interactions. , 1995, Shock.

[4]  V. Herzog,et al.  Extrathyroidal release of thyroid hormones from thyroglobulin by J774 mouse macrophages. , 1994, The Journal of clinical investigation.

[5]  K. Nouri-Aria,et al.  Effect of supernatants from Kupffer cells stimulated with galactosamine and endotoxin on the function of isolated rat hepatocytes. , 1993, Hepato-gastroenterology.

[6]  R. Sormunen,et al.  Bile canaliculus formation in cultured HEPG2 cells. , 1993, Laboratory investigation; a journal of technical methods and pathology.

[7]  A. Varki Biological roles of oligosaccharides: all of the theories are correct , 1993, Glycobiology.

[8]  J. Liu,et al.  Identification of a thyroid hormone response element in the phosphoenolpyruvate carboxykinase (GTP) gene. Evidence for synergistic interaction between thyroid hormone and cAMP cis-regulatory elements. , 1991, The Journal of biological chemistry.

[9]  J. Lau,et al.  Hepatology , 1999, Digestive Disease Interventions.

[10]  P. Romagnoli,et al.  Transcytosis in thyroid follicle cells: regulation and implications for thyroglobulin transport. , 1991, Experimental cell research.

[11]  K. Decker,et al.  Biologically active products of stimulated liver macrophages (Kupffer cells). , 1990, European journal of biochemistry.

[12]  D. Grieco,et al.  Thyroid hormone-mediated transcriptional activation of the rat liver malic enzyme gene by dehydroepiandrosterone. , 1989, The Journal of biological chemistry.

[13]  H. Geuze,et al.  Sorting of endocytosed transferrin and asialoglycoprotein occurs immediately after internalization in HepG2 cells , 1987, The Journal of cell biology.

[14]  T. V. van Berkel,et al.  The interaction in vivo of transferrin and asialotransferrin with liver cells. , 1987, The Biochemical journal.

[15]  M. Magnuson,et al.  Thyroid hormone regulation of malic enzyme synthesis. Dual tissue-specific control. , 1986, The Journal of biological chemistry.

[16]  B. Dozin,et al.  Tissue-specific control of rat malic enzyme activity and messenger RNA levels by a high carbohydrate diet. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[17]  S. Nagataki,et al.  Release of thyroid hormone from circulating thyroglobulin in the rat. , 1986, Acta endocrinologica.

[18]  K. Howell,et al.  Immuno‐isolation of a plasma membrane fraction from the Fao cell. , 1985, The EMBO journal.

[19]  S. Nagataki,et al.  Degradation of circulating thyroglobulin. , 1985, Metabolism: clinical and experimental.

[20]  M. Magnuson,et al.  Tissue-specific regulation of two functional malic enzyme mRNAs by triiodothyronine. , 1985, Biochemistry.

[21]  S. Swillens,et al.  Primary structure of bovine thyroglobulin deduced from the sequence of its 8,431-base complementary DNA , 1985, Nature.

[22]  V. Herzog Transcytosis in thyroid follicle cells , 1983, The Journal of cell biology.

[23]  C. Wu,et al.  Model for specific rescue of normal hepatocytes during methotrexate treatment of hepatic malignancy. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[24]  R. Cummings,et al.  Characterization of the structural determinants required for the high affinity interaction of asparagine-linked oligosaccharides with immobilized Phaseolus vulgaris leukoagglutinating and erythroagglutinating lectins. , 1982, The Journal of biological chemistry.

[25]  C C Howe,et al.  Human hepatocellular carcinoma cell lines secrete the major plasma proteins and hepatitis B surface antigen. , 1980, Science.

[26]  A. Schneider,et al.  Clearance of normal and tumor-related thyroglobulin from the circulation of rats: role of the terminal sialic acid residues. , 1980, Metabolism: clinical and experimental.

[27]  G. Wilson,et al.  An electron microscope autoradiographic study of the carbohydrate recognition systems in rat liver. I. Distribution of 125I-ligands among the liver cell types , 1979, The Journal of cell biology.

[28]  H. Towbin,et al.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[29]  Y. Suzuki,et al.  Clearance of circulating desialylated thyroglobulins in the rat. , 1979, Biochimica et biophysica acta.

[30]  T. Colacchio,et al.  Thyroglobulin in benign and malignant thyroid disease. , 1979, JAMA.

[31]  P. Larsen,et al.  Metabolic clearance of endogenous and radioiodinated thyroglobulin in rats. , 1978, Endocrinology.

[32]  P. Ralph,et al.  Lysozyme synthesis by established human and murine histiocytic lymphoma cell lines , 1976, The Journal of experimental medicine.

[33]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[34]  M. Cohn,et al.  Reticulum cell sarcoma: an effector cell in antibody-dependent cell-mediated immunity. , 1975, Journal of immunology.

[35]  M. Surks,et al.  Quantitation of extrathyroidal conversion of L-thyroxine to 3,5,3'-triiodo-L-thyronine in the rat. , 1971, The Journal of clinical investigation.

[36]  G. Gregoriadis,et al.  The role of sialic acid in determining the survival of glycoproteins in the circulation. , 1971, The Journal of biological chemistry.

[37]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[38]  I. Roitt,et al.  Identification and estimation of undegraded thyroglobulin in human serum. , 1967, Endocrinology.

[39]  E. Assem THYROGLOBULIN IN THE SERUM OF PARTURIENT WOMEN AND NEWBORN INFANTS. , 1964, Lancet.

[40]  T. Hjort Determination of serum-thyroglobulin by a haemagglutination-inhibition test. , 1961, Lancet.

[41]  H. Jackson,et al.  The fate of 131I-labelled homologous and heterologous thyroglobulins in the rat, dog, monkey and rabbit. , 1956, The Biochemical journal.

[42]  K. Burton A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid. , 1956, The Biochemical journal.

[43]  T. Billiar,et al.  Liver nonparenchymal cells are stimulated to provide interleukin 6 for induction of the hepatic acute-phase response in endotoxemia but not in remote localized inflammation. , 1992, Archives of surgery.

[44]  R. Dernick,et al.  Improved silver staining procedure for fast staining in PhastSystem Development Unit. I. Staining of sodium dodecyl sulfate gels , 1988, Electrophoresis.

[45]  V. Herzog,et al.  Pathways of endocytosis in thyroid follicle cells. , 1984, International review of cytology.

[46]  G. Ashwell,et al.  Carbohydrate-specific receptors of the liver. , 1982, Annual review of biochemistry.