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V-Ras and V-Raf Block Differentiation of Transformable C3h10t1/2-Derived Preadipocytes At Lower Levels Than Required For Neoplastic Transformation

  1. Author:
    Raptis, L.
    Brownell, H. L.
    Lu, Y.
    Preston, T.
    Narsimhan, R. P.
    Anderson, S.
    Schaefer, E.
    Haliotis, T.
  2. Author Address

    Raptis L QUEENS UNIV DEPT MICROBIOL & IMMUNOL KINGSTON ON CANADA QUEENS UNIV DEPT PATHOL KINGSTON ON CANADA HARVARD UNIV SCH MED DANA FARBER CANC INST CAMBRIDGE, MA 02138 USA NCI FREDERICK, MD 21702 USA PROMEGA CORP MADISON, WI 53711 USA
    1. Year: 1997
  1. Journal: Experimental Cell Research
    1. 235
    2. 1
    3. Pages: 188-197
  2. Type of Article: Article
  1. Abstract:

    To investigate the functional relationship between the transforming ability of Ras and its role as an integral component of the differentiative insulin signaling pathway, we introduced a leu61-activated ms gene into a Ras-transformable, C3H1OT1/2-derived preadipocytic cell line. The results demonstrate that ras(leu61) expression in this Line blocks differentiation and that this block. appears at lower levels than required for full. neoplastic transformation, In addition, to examine whether the inability of Ras(leu61) to induce differentiation by replacing the insulin signal could be attributed to its transforming effect in this system, we examined the effect of Ras(leu61) at levels below the baseline, by expressing ras(leu61) in a series of preadipocytes which were rendered deficient in endogenous c-Ras activity, The results show that even very low Ras(leu61) levels, insufficient to restore the growth rate of these cells to normal, blocked rather than enhanced differentiation, indicating that ras(leu61) expression alone is not sufficient to promote adipocytic differentiation in this system, even in the absence of neoplastic transformation. Consistent with its established role as a downstream effector of Ras, v-Raf expression mirrored the v-Ras effects upon adipocytic differentiation and transformation. (C) 1997 Academic Press. [References: 42]

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