Loss of several cell functions including okadaic acid-induced apoptosis after multiple passages in FRTL-5 cells

Molecular and Cellular Endocrinology

Volumn 150, Issue 1-2, 1999, Pages 141-149

  Golstein, J ^a   Kimura, T ^a   Miot, F ^a   Dumont, J E ^a  

^a FREE UNIVERSITY OF BRUSSELS   (Belgium)

Author keywords

Aging; Apoptosis; FRTL 5 cells; Proliferation

Indexed keywords

CELL DNA; INSULIN; IODIDE; MESSENGER RNA; THYMIDINE; THYROGLOBULIN; TRITIUM;

AGING; ANIMAL CELL; APOPTOSIS; ARTICLE; CELL FUNCTION; CELL PROLIFERATION; CONTROLLED STUDY; MITOGENESIS; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; RAT; THYROID CELL;

ANIMALS; APOPTOSIS; CELL AGING; CELL DIVISION; CELL LINE; ENZYME INHIBITORS; OKADAIC ACID; RATS; THYROID GLAND; THYROTROPIN;

EID: 0033602681     PISSN: 03037207     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0303-7207(99)00009-X     Document Type: Article

References (27)

1. Ambesi-Impiombato F.S., Picone R., Tramontano D. Growth of Cells in Hormonally Defined Media. 9:1982;483-492 Cold Spring Harbor Laboratory, New York.
2. Ambesi-Impiombato F.S., Parks L.A.M., Coon H.G. Culture of hormone-dependent functional epithelial cells from rat thyroids. Proc. Natl. Acad. Sci. USA. 77:1980;3455-3459.
3. Bellur S., Tahara K., Saji M., Grollman E.F., Kohn L.D. Repeatedly passed FRTL-5 rat thyroid cells can develop insulin and insulin-like growth factor-I-sensitive cyclooxygenase and prostaglandin E2 isomerase-like activities together with altered basal and thyrotropin-responsive thymidine incorporation into DNA. Endocrinology. 127:1990;1526-1540.
4. Bertrand F., Atfi A., Cadoret A., L'Allemain G., Robin H., Lascols O., Capeau J., Cherqui G. A role for nuclear factor KB in the antiapoptotic function of insulin. J. Biol. Chem. 273:1998;2931-2938.
5. Chen G., Pekary A.E., Hershman J.M. Aging of FRTL-5 rat thyroid cells causes sensitivity to cytotoxicity induced by tumor necrosis factor-α Endocrinology. 131:1992;863-870.
6. D'Ambrosio C., Valentinis B., Prisco M., Reiss K., Rubini M., Baserga R. Protective effect of the insulin-like growth factor I receptor on apoptosis induced by okadaic acid. Cancer Research. 57:1997;3264-3271.
7. Depoortere F., Van Keymeulen A., Lukas J., Costagliola S., Bartkova J., Dumont J.E., Bartek J., Roger P.P., Dremier S. A requirement for cyclin D3-Cyclin-dependent kinase (cdk)-4 assembly, in the cyclic adenosine monophosphate-dependent pro1iferation of thyrocytes. J. Cell Biol. 140:1998;1427-1439.
8. Dumont J.E., Roger P.P., Ludgate M. Assays for thyroid growth immunoglobulins and their clinical implications: methods,concepts and misconceptions. Endocr. Rev. 8:1987;448-452.
9. Farid N.R., Shi Y., Zou M. Molecular basis of thyroid cancer. Endocr. Rev. 15:1994;202-232.
10. Francis-Lang H., Zannini M., De Felice M., Berlingieri M.T., Fusco A., Di Lauro R. Multiple mechanisms of interference between transformation and differentiation in thyroid cells. Mol. Cell. Biol. 12:1992;5793-5800.
11. Fujiki H., Suganuma M. Tumor promotion by inhibitors of protein phosphatases 1 and 2A: the okadaic acid class of compounds. Adv. Cancer Res. 61:1993;143-167.
12. Golstein J., Swillens S., Dumont J.E. Comparative cytotoxic effects of two protein phosphatase inhibitors, okadaic acid and calyculin A, on thyroid cells. Cell Death Diff. 2:1995;321-329.
13. Grigoriev V.G., Moerman E.J., Goldstein S. Overexpression of insulin-like growth factor binding protein-3 by senescent human fibroblasts: attenuation of the motogenic response to IGF-1. Exp. Cell Res. 219:1995;315-321.
14. Lazzereschi D., Coppa A., Mincione G., Lavitrano M., Fragomele F., Colletta G. The phosphatase inhibitor okadaic acid stimulates the TSH-induced G1-S phase transition in thyroid cells. Exp. Cell Res. 234:1997;425-433.
15. Maciel Rui M.B., Moses A.C., Villone G., Tramontano D., Ingbar S.H. Demonstration of the production and physiological role of insulin-like growth factor II in rat thyroid follicular cells in culture. J. Clin. Invest. 82:1988;1546-1553.
16. - symporter messenger ribonucleic acid levels in FRTL-5 cells. Endorinology. 139:1998;703.
17. Pekary A.E., Berg L., Wang J., Lee P., Dubinett S.M., Hershman J.M. TNF-α, TSH, and aging regulate TGF-β synthesis and secretion in FRTL-5 rat thyroid cells. Am. J. Physiol. 268:1995;R808-R815.
18. Pohl V., Roger P.P., Christophe D., Pattyn G., Vassart G., Dumont J.E. Differentiation expression during proliferative activity induced through different pathways: in situ hybridization study of thyroglobulin gene expression in thyroid epithelial cells. J. Cell Biol. 111:1990;663-672.
19. Roger P.P., Hotimsky A., Moreau C., Dumont J.E. Stimulation by thyrotropin, cholera toxin;: and dibutyryl cyclic AMP of the multiplication of differentiated thyroid cells in vitro. Mol. Cell. Endocrinol. 26:1982;165-176.
20. Roger P.P., Reuse S., Servais P., Van Heuverswyn B., Dumont J.E. Stimulation of cell proliferation and inhibition of differentiation expression by tumor-promoting phorbol esters in dog thyroid cells in primary culture. Cancer Res. 46:1986;898-906.
21. Sambrook, J., Fritish, E.F., Maniatis, T., 1989. Molecular Cloning: a Laboratory Manual, second ed. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York.
22. Stein G.H., Beeson M., Gordon L. Failure to phosphorylate the retinoblastoma gene product in senescent human fibriblasts. Science. 249:1990;666-669.
23. Tramontano D., Moses A.C., Ingbar S.H. The role of adenosine 3′,5′ monophosphate in the regulation of receptors for thyrotropin and insulin-like growth factor I in the FRTL-5 rat thyroid follicular cell. Endocrinology. 122:1988;133-136.
24. Tramontano D., Moses A.C., Veneziani B.M., Ingbar S.H. Adenosine 3′,5′ monophosphate mediates both the mitogenic effect of thyrotropin and its ability to amplify the response to insulin-like growth factor I in FRTL-5 cells. Endocrinology. 122:1988;127-132.
25. Tramontano D., Rotella C.M., Toccafondi R., Ambesi-Impiombato F.S. Thyrotropin-independent mutant clones from FRTL-5 rat thyroid cells: hormonal control mechanisms in differentiated cells. Endocrinology. 118:1986;862-868.
26. - symporter mRNAs in dog thyroid. Mol. Cell. Endocrinol. 131:1997;195-203.
27. Weiss S.J., Philp N.J., Ambesi-Impiombato F.S., Grollman E.F. Thyrotropin-stimulated iodide transport mediated by adenosine 3′,5′-monophosphate and dependent on protein synthesis. Endocrinology. 114:1984;1099-1107.