Hexamethylene bisacetamide (HMBA) increases thyroglobulin levels in porcine thyroid cells without increasing Cyclic-AMP

Hormone and Metabolic Research

Volumn 31, Issue 7, 1999, Pages 402-405

  Aouani, A ^a   Samih, N ^a   Amphoux Fazekas, T ^a   Mezghrani, A ^a   Mykhaylov, S ^b   Hovsepian S ^a   Lombardo, D ^a   Fayet, G ^a  

^a INSERM   (France)

^b Institute of Pharmacology and Toxicology   (Ukraine)

Author keywords

Cyclic AMP; HMBA; Thyroglobulin; Thyroid; Thyroid Cells

Indexed keywords

CYCLIC AMP; HEXAMETHYLENEBISACETAMIDE; THYROGLOBULIN;

ANIMAL CELL; ARTICLE; CELL CULTURE; CELL LEVEL; HORMONAL REGULATION; HORMONE ACTION; NONHUMAN; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN LOCALIZATION; THYROID CELL;

ANIMALIA; MURINAE; SUIDAE;

EID: 0032781689     PISSN: 00185043     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-978763     Document Type: Article

References (30)

1. 1 Friend C, Scher W, Holland JG, Sato T. Hemoglobin synthesis in murine virus-induced leukemic cells in vitro: stimulation of erythroid differentiation by dimethyl sulfoxide. Proc Natl Acad Sci USA 1971; 68: 378-382
2. 2 Marks PA, Rifkind RA. Erythroleukemic differentiation. Annu Rev Biochem 1978; 47: 419-448
3. 3 Fibach E, Reuben RC, Rifkind RA, Marks PA. Effect of hexamethylene bisacetamide on the commitment to terminal differentiation of murine erythroleukemia cells. Cancer Res 1977; 37: 440-444
4. 4 Marks PA, Rifkind RA. Differentiation modifiers. Cancer 1984; 54: 2766-2769
5. 5 Fayet G, Amphoux-Fazekas T, Aouani A, Hovsépian S. Hexamethylene bisacetamide (HMBA) is a growth factor for human, ovine and porcine thyroid cells. Mol Cell Endocrinol 1996; 117: 111-116
6. 6 Amphoux-Fazekas T, Fayet G, Hovsépian S, Aouani A, Samih N. Hexamethylene bisacetamide (HMBA) prevents the loss of TSH-sensitivity in porcine thyroid monolayer cells. C R Acad Sci Paris 1997; 320: 1-11
7. 7 Amphoux-Fazekas T, Fayet G, Hovsépian S, Aouani A, Samih N. Hexamethylene bisacetamide (HMBA) induces follicle formation, prevents the loss in cell-TSH sensitivity but inhibits iodide metabolism and decreases cell protein levels in porcine thyroid cells. J Endocrinol Invest 1997; 20 (Suppl.): S42
8. 8 Fayet G, Hovsépian S. Active transport of iodide in isolated porcine thyroid cells. Application to an in vitro bioassay of thyrotropin. Mol Cell Endocrinol 1977; 7: 67-78
9. 9 Chambard M, Gabrion J, Mauchamp J. Influence of collagen gel on the orientation of epithelial polarity: follicle formation from isolated cells and from performed monolayers. J Cell Biol 1981; 91: 157-166
10. 10 Fayet G, Hovsépian S, Dickson JG, Lissitzky S. Reorganization of porcine thyroid cells into functional follicles in a chemically defined, serum-and thyrotropin-free medium. J Cell Biol 1982; 93: 479-488
11. -15 mole level. Anal Biochem 1973; 56: 394-407
12. 12 Fayet G, Aouani A, Hovsépian S. TSH-induced cyclic AMP production in an ovine thyroid cell line: OVNIS 5H. FEBS Lett 1986; 194: 287-291
13. 13 Minamide LS, Bambourg JR. A filter paper dye-binding assay for quantitative determination of protein without interference from reducing agents or detergents. Anal Biochem 1990; 190: 66-70
14. 14 Labarca C, Païgen K. A simple, rapid and sensitive DNA assay procedure. Anal Biochem 1980; 102: 344-352
15. 15 Lissitzky S, Fayet G, Verrier B, Hennen G, Jaquet P. Thyroid-stimulating hormone binding to cultured thyroid cells. FEBS Lett 1973; 29: 20-24
16. 16 Chebath J, Chabaud O, Mauchamp J. Modulation of thyroglobulin messenger RNA level by thyrotropin in cultured thyroid cells. Nucleic Acids Res 1979; 6: 3353-3367
17. 17 Avvedimento VE, Tramontano D, Ursin NV, Monticelli A, Di Lauro R. The level of thyroglobulin mRNA is regulated by TSH both in vitro and in vivo. Biochem Biophys Res Commun 1984; 122: 472-477
18. 18 Aouani A, Hovsépian S, Fayet G. cAMP dependent and independent regulation of thyroglobulin synthesis by two clones of the OVNIS 6H thyroid cell line. Mol Cell Endocrinol 1987; 52: 151-160
19. 19 Gilman AG, Rall TW. Factors influencing adenosine 3′,5′ phosphate accumulation in bovine thyroid slices. J Biol Chem 1968; 243: 5867-5871
20. 20 Van Heuverswyn B, Leriche A, Van Sande J, Dumont JE, Vassart G. Transcriptional control of thyroglobulin gene expression by cyclic AMP, FEBS Lett 1988; 188: 192-196
21. 21 Fayet G, Lissitzky S. Cyclic 3′,5′-adenosine monophosphate-mediated follicular reorganization of isolated thyroid cells in culture. FEBS Lett 1970; 11: 185-188
22. 22 Gazitt Y, Reuben RC, Deitch AD, Marks PA, Rifkind RA. Changes in cAMP levels during induction of differentiation in murine erythroleukemia cells. Cancer Res 1978; 38: 3779-3783
23. 23 Michaeli J, Busquets X, Orlow I, Younes A, Colomer D, Marks PA, Rifkind RA, Kolesnick RN. A rise and fall in 1,2-diacylglycerol content signal hexamethylene bisacetamide induced-erythropoeisis. J Biol Chem 1992; 267: 23463-23466
24. 24 Pessino A, Passalacqua M, Sparatore B, Patrone M, Melloni E, Pontremoli S. Antisense oligonucleotide inhibition of protein kinase C expression accelerates induced differentiation of murine erythroleukaemia cells. Biochem J 1995; 312: 549-554
25. 25 Kiyokawa H, Richon VM, Rifkind RA, Marks PA. Suppression of cyclin-dependent kinase 4 during induced differentiation of erythroleukemia cells. Mol Cell Biol 1994; 14: 7195-7203
26. 26 Coppola JA, Dole MD. Constitutive c-myc oncogene expression blocks mouse erythroleukemia cell differentiation but not commitment. Nature 1986; 320: 760-763
27. 27 Richon VM, Rifkind RA, Marks PA. Expression of phosphorylation of the retinoblastoma protein during induced differentiation of murine erythroleukemia cells. Cell Growth Differ 1992; 3: 413-420
28. 28 Kennedy BG, Lever JE. Transport by the (Na+, K+) ATPase: modulation by differentiation inducers and inhibition of protein synthesis in the MDCK kidney epithelial cell line. J Cell Physiol 1985; 123: 410-416
29. 29 Reuben RC, Rifkin RA, Marks PA. Chemically induced erythroleukemia differentiation. Biochem Biophys Res Commun 1980; 605: 325-346
30. 30 Reuben RC. Studies on the mechanism of action of hexamethylene bisacetamide, a potent inducer of erythroleukemic differentiation. Biochim Biophys Acta 1979; 588: 310-321