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Growth stimulation of murine fibroblasts by TGF-β1 depends on the expression of a functional p53 protein

Abstract

Transforming Growth Factor-β1 (TGF-β1) inhibits the proliferation of most cells, but stimulates some mesenchymal cell types, including murine NIH3T3 fibroblasts. We show here that TGF-β1 growth stimulation of NIH3T3 fibroblasts is reversed when these cells are transformed by SV40 or are transfected with a plasmid encoding the SV40 Large T antigen. Inversion of the TGF-β1 growth stimulation of NIH3T3 cells is not observed when these cells are transfected with plasmids expressing either a mutant Large T, unable to bind P53, or the E1A adenovirus oncoprotein which binds the retinoblastoma protein pRB but not P53. But when the TGF-β1-growth stimulated cells are transfected with a plasmid expressing a mutant form of Large T capable of binding to P53, but not to pRB, or with one expressing the E1B-55 kD adenovirus oncoprotein, which also binds to P53 but not to pRB, the cells are growth-inhibited by TGF-β1. The cdk inhibitor p21Waf is decreased in TGF-β1-stimulated NIH3T3 fibroblasts and increased in TGF-β1-inhibited SV40-transformed cells. Finally, we show that T12 fibroblasts, from a P53 knockout mouse, are growth inhibited by TGF-β1 and that they remain so upon transfection with a P53 which is mutant at restrictive temperature, but become growth-stimulated by this factor at permissive temperature when P53 is functional. These data strongly suggest that growth-stimulation of fibroblasts by TGF-β1 depends on the presence of a functional P53 protein and that inversion of this response occurs if P53 is absent or inactivated.

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References

  • Alexandrow MG and Moses HL. . 1995 Cancer Res. 55: 1452–1457.

  • Benoist C and Chambon P. . 1981 Nature 290: 304–309.

  • Benzakour O, Merzak A, Dooghe Y, Pironin M, Lawrence D and Vigier P. . 1992 Growth Factors 6: 265–275.

  • Blaydes JP, Schlumberger M, Wynford-Thomas D and Wyllie FS. . 1995 Oncogene 10: 307–317.

  • Daniel TO, Gibbs VC, Milfray DF and Williams LT. . 1987 J. Biol. Chem. 262: 11893–11896.

  • DeCaprio JA, Ludlow JW, Figge J, Shew CJY, Huang CM, Lee WH, Marsilio E, Paucha E and Livingston DM. . 1988 Cell 54: 275–283.

  • Derynck R. . 1994 Trends Biochem. Sci. 19: 548–553.

  • Dive C, Gregory CD, Phipps DJ, Evans DL, Milner AE and Wyllie AH. . 1992 Biochemica et Biophysica Acta. 1133: 275–285.

  • Donehover LA, Harvey M, Slagle BL, McArthur MG, Montgomery Jn CA, Butel JS and Bradley A. . 1992 Nature 356: 215–221.

  • El-Deiry WS, Tokino T, Velculescu VE, Levy DB, Parsons R, Trent JM, Lin D, Mercer E, Kinzler KW and Vogelstein B. . 1993 Cell 75: 817–825.

  • Evangelisti R, Valeno V, Bodo M, Bosi G, Stabellini G and Carinci P. . 1997 Cell Biochem. Func. 15: 47–51.

  • Finlay CA, Hinds PW, Tan TH, Eliyahu D, Oren M and Levine AJ. . 1988 Mol. Cell. Biol. 8: 531–539.

  • Gregoire M, Hernandez-Verdum D and Bouteille M. . 1984 Exp. Cell Res. 152: 38–46.

  • Hannon GJ and Beach D. . 1994 Nature 371: 257–261.

  • Heldin C-H, Miyazono K and ten Dijke P. . 1997 Nature 390: 465–471.

  • Hill DJ, Strain AJ, Elstow SF, Swenne I and Milner RDG. . 1986 J. Cell. Physiol. 128: 322–328.

  • Huang F, Hsu S, Yan Z, Winawer S and Friedman E. . 1994 Oncogene 9: 3701–3706.

  • Jochemsen AG, Peltenburg LTC, te Pas MFW, de Wit CM, Bos JL and van der Eb AJ. . 1987 EMBO J. 6: 3399–3405.

  • Kalderon D and Smith AE. . 1984 Virology 139: 109–137.

  • Kim TA, Cutry AF, Kinniburgh AJ and Wenner CE. . 1993 Cancer Letters 71: 125–132.

  • Kim TA, Ravitz MJ and Wenner CE. . 1994 J. Cell. Physiol. 160: 1–9.

  • Koike M, Ishino K, Huh N and Kuroki T. . 1994 Biochem. Biophys. Res. Comm. 201: 673–681.

  • Laiho M, DeCaprio JA, Ludlow JW, Livingston DM and Massagué J. . 1990 Cell 62: 175–185.

  • Lawrence DA. . 1995 Kidney Int. 47: S19–S23.

  • Leof EB, Proper JA, Goustin AS, Shipley GD, DiCorletto PE and Moses HL. . 1986 Proc. Natl. Acad. Sci. USA 83: 2453–2457.

  • Machwate M, Jullienne A, Moukhtar M, Lomri A and Marie PJ. . 1995 Mol. Endocrinol. 9: 187–198.

  • Malliri A, Yeudall A, Nikolic M, Crouch DH, Parkinson EK and Ozanne B. . 1996 Cell Growth & Differ. 7: 1291–1304.

  • Manfredi JJ and Prives C. . 1994 Biochim. Biophys. Acta. 1198: 65–83.

  • Massagué J and Polyak K. . 1995 Current Opin. Genet. Dev. 5: 91–96.

  • Michalovitz D, Halevy O and Oren M. . 1990 Cell 62: 671–680.

  • Michieli P, Chedid M, Lin D, Pierce JH, Mercer WE and Givol D. . 1994 Cancer Res. 54: 3391–3395.

  • Milner J and Medcalf E. . 1990 J. Mol. Biol. 216: 481–484.

  • Muller W and Gauthier F. . 1975 Eur. J. Biochem. 54: 385–394.

  • Nagy JA, Brown LF, Senger DR, Lanir N, Van de Water L, Dvorak AM and Dvorak HF. . 1988 Biochim. Biophys. Acta. 948: 305–326.

  • Okadome T, Yamashita H, Franzén P, Morén A and Heldin C-H. . 1994 J. Biol. Chem. 269: 30753–30756.

  • Ong G, Sikora K and Gullick WJ. . 1991 Oncogene 6: 761–763.

  • Ormerod MG, Collins MKL, Rodriguez-Tarduchy G and Robertson D. . 1992 J. Immunol. Methods 153: 57–65.

  • Pipas JM, Peden KW and Nathans D. . 1983 Mol. Cell. Biol. 3: 203–213.

  • Ravitz MJ, Yan S, Herr KD and Wenner CE. . 1995 Cancer Res. 55: 1413–1416.

  • Raynal S, Jullien P and Lawrence DA. . 1994 Growth Factors 11: 197–203.

  • Raynal S and Lawrence DA. . 1995 Int. J. Oncol. 7: 337–341.

  • Reynisdottir I, Polyak K, Iavarone A and Massagué J. . 1995 Genes & Development 9: 1831–1845.

  • Roberts AB and Sporn MB. . 1990 In Handbook of Experimental Pharmacology (eds.) MB Sporn and AB Roberts vol. 95 I Peptide Growth Factors and their Receptors Springer-Verlag.

    Google Scholar 

  • Sarnow P, Ho YS, Williams J and Levine AJ. . 1982 Cell 28: 387–394.

  • Sgamboto A, Doki Y, Schieren I and Weinstein IB. . 1997 Cell Growth Differ. 8: 393–405.

  • Ventura F, Doody J, Liu F, Wrana JL and Massagué J. . 1994 EMBO J. 13: 5581–5589.

  • Watabe K, Fukuda T, Tanaka J, Toyohara K and Sakai O. . 1994 J. Neurosci. Res. 39: 525–534.

  • Whyte P, Buchkovich KJ, Horowitz JM, Friend SH, Raybuck M, Weinberg RA and Harlow E. . 1988 Nature 334: 124–129.

  • Zantema A, Fransen JAM, Davis-Olivier A, Ramaekers FCS, Vooijis GP, DeLeys B and van der Eb AJ. . 1985 Virology 142: 44–58.

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Acknowledgements

We thank Drs E and P May, A Zantema, AJ van der Eb and D Trouche for supplying certain reagents and Zohar Mischal for the flow cytometry analysis. This work received financial suport from the `Association de Recherche sur le Cancer' and the Fondation de France. F.D. was financed by the `Association de Recherche sur le Cancer' (96-97) and by the `Ligue Nationale Contre le Cancer, Comité de l'Essonne' (97-98). SR received support from the `Fondation Singer-Polignac'. This work was started whilst all the authors were still at the Institut Curie, Orsay.

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Dkhissi, F., Raynal, S., Jullien, P. et al. Growth stimulation of murine fibroblasts by TGF-β1 depends on the expression of a functional p53 protein. Oncogene 18, 703–711 (1999). https://doi.org/10.1038/sj.onc.1202341

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