[go: up one dir, main page]
More Web Proxy on the site http://driver.im/
Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Macrophage-induced angiogenesis is mediated by tumour necrosis factor-α

Abstract

Macrophages are important in the induction of new blood vessel growth during wound repair, inflammation and tumour growth1–4. We show here that tumour necrosis factor-α (TNF-α), a secretory product of activated macrophages that is believed to mediate tumour cytotoxicity5–9, is a potent inducer of new blood vessel growth (angiogenesis). In vivo, TNF-α induces capillary blood vessel formation in the rat cornea and the developing chick chorioallantoic membrane at very low doses. In vitro, TNF-α stimulates chemotaxis of bovine adrenal capillary endothelial cells and induces cultures of these cells grown on type-1 collagen gels to form capillary-tube-like structures. The angiogenic activity produced by activated murine peritoneal macrophages is completely neutralized by a polyclonal antibody to TNF-α, suggesting immunological features are common to TNF-α and the protein responsible for macrophage-derived angiogenic activity. In inflammation and wound repair, TNF-α could augment repair by stimulating new blood vessel growth; in tumours, TNF-α might both stimulate tumour development by promoting vessel growth and participate in tumour destruction by direct cytotoxicity10–12.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Leibovich, S. J. & Ross, R. Am. J. Path. 78, 71–100 (1975).

    CAS  PubMed  Google Scholar 

  2. Polverini, P. J., Cotran, R. S., Gimbrone, M. A. Jr & Unanue, E. R. Nature 269, 804–806 (1977).

    Article  ADS  CAS  Google Scholar 

  3. Clark, R. A. et al. Surg. Forum. 27, 16–22 (1976).

    CAS  PubMed  Google Scholar 

  4. Polverini, P. J. & Leibovich, S. J. Lab. Invest. 51, 635–642 (1985).

    Google Scholar 

  5. Nathan, C. F. J. clin. Invest. 79, 319–326 (1987).

    Article  CAS  Google Scholar 

  6. Carswell, E. A. et al. Proe. natn. Acad. Sci. U.S.A. 72, 3666–3670 (1975).

    Article  ADS  CAS  Google Scholar 

  7. Ruff, M. & Gifford, G. E. in Lymphokine Reports, 2 (ed. Pick, E.) 235–272 (Academic, New York, 1985).

    Google Scholar 

  8. Beutler, B. & Cerami, A. Nature 320, 584–588 (1986).

    Article  ADS  CAS  Google Scholar 

  9. Urban, J. L., Shepard, H. M., Rothstein, J. L., Sugarman, B. J. & Schreiber, H. Proc. natn. Acad. Sci. U.S.A. 83, 5233–5237 (1986).

    Article  ADS  CAS  Google Scholar 

  10. Sugarman, B. J. et al. Science 230, 943–945 (1985).

    Article  ADS  CAS  Google Scholar 

  11. Banda, M. J., Knighton, D. R., Hunt, T. K. & Werb, Z. Proc. natn. Acad. Sci. U.S.A. 79, 7773–7777 (1982).

    Article  ADS  CAS  Google Scholar 

  12. Koch, A. E., Polverini, P. J. & Leibovich, S. J. Arthritis Rheum. 29, 471–479 (1986).

    Article  CAS  Google Scholar 

  13. Shing, Y. et al. J. cell. Biochem. 29, 275–287 (1985).

    Article  CAS  Google Scholar 

  14. Thomas, K. A., Rios-Candelore, M., Gimenez-Gallego, G., Rodkey, J. & Fitzpatrick, S. Proc. natn. Acad. Sci. U.S.A. 82, 6409–6413 (1985).

    Article  ADS  CAS  Google Scholar 

  15. Esch, F. et al. Proc. natn. Acad. Sci. U.S.A. 82, 6507–6511 (1985).

    Article  ADS  CAS  Google Scholar 

  16. Fett, J. W. et al. Biochemistry 24, 5480–5486 (1985).

    Article  CAS  Google Scholar 

  17. Schreiber, A. B., Winkler, M. E. & Derynck, R. Science 232, 1250–1252 (1986).

    Article  ADS  CAS  Google Scholar 

  18. Beutler, B. et al. Nature 316, 552–554 (1985).

    Article  ADS  CAS  Google Scholar 

  19. Le, J. & Vilcek, J. Lab. Invest. 56, 234–248 (1987).

    CAS  PubMed  Google Scholar 

  20. Sato, N. et al. Proc. Japan Acad. 61, 471–474 (1985).

    Article  CAS  Google Scholar 

  21. Beutler, B., Tkacenko, V., Milsark, I., Krochin, N. & Cerami, A. J. exp. Med. 164, 1791–1796 (1986).

    Article  CAS  Google Scholar 

  22. Koch, A. E., Polverini, P. J. & Leibovich, S. J. J. Leukocyte Biol. 39, 233–238 (1986).

    Article  CAS  Google Scholar 

  23. Wiseman, D., Polverini, P. J., Kamp, D. & Leibovich, S. J. J. Cell Biol. (in the press).

  24. Assoian, R. K. & Sporn, M. B. J. cell Biol. 102, 1217–1223 (1986).

    Article  CAS  Google Scholar 

  25. Klagsburn, M., Sasse, J., Sullivan, R. & Smith, J. A. Proc. natn. Acad. Sci. U.S.A. 83, 2448–2452 (1986).

    Article  ADS  Google Scholar 

  26. Schweigerer, L. et al. Nature 325, 257–259 (1987).

    Article  ADS  CAS  Google Scholar 

  27. Denekamp, J. in Progress Microcirculation Vol. 42 (eds Hammersen, F. & Hudlicka, O.) 28–38 (Karger, Basel, 1984).

    Google Scholar 

  28. Baird, A., Mormede, P. & Bohlen, P. Biochem. biophys. Res. Commun. 126, 358–364 (1985).

    Article  CAS  Google Scholar 

  29. Montesano, R. & Orci, L. Cell 42, 469–477 (1985).

    Article  CAS  Google Scholar 

  30. Leibovich, S. J. & Polverini, P. J. Br. J. Rheumatol. 24, 197–202 (1985).

    Article  Google Scholar 

  31. Folkman, J., Haudenschild, C. C. & Zetter, B. R. Proc. natn. Acad. Sci. U.S.A. 76, 5217–5221 (1979).

    Article  ADS  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Leibovich, S., Polverini, P., Shepard, H. et al. Macrophage-induced angiogenesis is mediated by tumour necrosis factor-α. Nature 329, 630–632 (1987). https://doi.org/10.1038/329630a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/329630a0

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing