This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yu, C L
Right arrow Articles by Stacey, D W
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yu, C L
Right arrow Articles by Stacey, D W

 Previous Article  |  Next Article 

Mol Cell Biol. 1990 December; 10(12): 6683-6689

Serum stimulation of NIH 3T3 cells induces the production of lipids able to inhibit GTPase-activating protein activity.

C L Yu, M H Tsai and D W Stacey

Department of Molecular Biology, Cleveland Clinic Foundation, Ohio 44106.

ABSTRACT

Quiescent NIH 3T3 cells were stimulated with serum prior to the extraction of total cellular lipids. These lipids were fractionated on thin-layer chromatography plates, and individual fractions were tested for the ability to inhibit GTPase-activating protein (GAP) activity. Two separate GAP inhibitory lipids were produced. One behaved similarly to arachidonic acid during silica gel chromatography, whereas the other was related to a phosphoinositide. Further study of the arachidonic acid-related material indicated that it was produced between 1 and 5 min after serum addition but was never observed in high-density, contact-inhibited cultures. The identity of these lipids is under investigation. The possibility raised by these results, that a metabolite of arachidonic acid is involved in mitogenic signaling, was supported by the finding that several lipoxygenase products of arachidonic acid efficiently inhibited GAP activity. These results provide further support for the hypothesis that lipids, GAP, and ras activity function together in the control of cellular proliferation.


Mol Cell Biol. 1990 December; 10(12): 6683-6689




This article has been cited by other articles:

  • Collett, E. D., Davidson, L. A., Fan, Y.-Y., Lupton, J. R., Chapkin, R. S. (2001). n-6 and n-3 polyunsaturated fatty acids differentially modulate oncogenic Ras activation in colonocytes. Am. J. Physiol. Cell Physiol. 280: C1066-C1075 [Abstract] [Full Text]  
  • Llorente, A, van Deurs, B, Garred, O, Eker, P, Sandvig, K (2000). Apical endocytosis of ricin in MDCK cells is regulated by the cyclooxygenase pathway. J. Cell Sci. 113: 1213-1221 [Abstract]  
  • Sun, C.-W., Falck, J. R., Harder, D. R., Roman, R. J. (1999). Role of Tyrosine Kinase and PKC in the Vasoconstrictor Response to 20-HETE in Renal Arterioles. Hypertension 33: 414-418 [Abstract] [Full Text]  
  • Mills, E. M., Takeda, K., Yu, Z.-X., Ferrans, V., Katagiri, Y., Jiang, H., Lavigne, M. C., Leto, T. L., Guroff, G. (1998). Nerve Growth Factor Treatment Prevents the Increase in Superoxide Produced by Epidermal Growth Factor in PC12 Cells. J. Biol. Chem. 273: 22165-22168 [Abstract] [Full Text]  
  • Jiang, Y., Lu, Z., Zang, Q., Foster, D. A. (1996). Regulation of Phosphatidic Acid Phosphohydrolase by Epidermal Growth Factor. REDUCED ASSOCIATION WITH THE EGF RECEPTOR FOLLOWED BY INCREASED ASSOCIATION WITH PROTEIN KINASE Cepsilon. J. Biol. Chem. 271: 29529-29532 [Abstract] [Full Text]  
  • Schubert, C., Carel, K., DePaolo, D., Leitner, W., Draznin, B. (1996). Interactions of Protein Kinase C with Insulin Signaling. INFLUENCE ON GAP AND SOS ACTIVITIES. J. Biol. Chem. 271: 15311-15314 [Abstract] [Full Text]  
  • Sermon, B. A., Eccleston, J. F., Skinner, R. H., Lowe, P. N. (1996). Mechanism of Inhibition by Arachidonic Acid of the Catalytic Activity of Ras GTPase-activating Proteins. J. Biol. Chem. 271: 1566-1572 [Abstract] [Full Text]  
  • Kim, J. A., Gu, J.-L., Natarajan, R., Berliner, J. A., Nadler, J. L. (1995). A Leukocyte Type of 12-Lipoxygenase Is Expressed in Human Vascular and Mononuclear Cells : Evidence for Upregulation by Angiotensin II. Arterioscler. Thromb. Vasc. Bio. 15: 942-948 [Abstract] [Full Text]  
  • Gu, J.-L., Veerapanane, D., Rossi, J., Natarajan, R., Thomas, L., Nadler, J. (1995). Ribozyme-Mediated Inhibition of Expression of Leukocyte-type 12-Lipoxygenase in Porcine Aortic Vascular Smooth Muscle Cells. Circ. Res. 77: 14-20 [Abstract] [Full Text]  
  • Han, J., McCormick, F, Macara, I. (1991). Regulation of Ras-GAP and the neurofibromatosis-1 gene product by eicosanoids. Science 252: 576-579 [Abstract]