Skip to main content

Advertisement

Log in

Lymphocyte-induced angiogenesis factor is produced by L3T4+ murine T lymphocytes, and its production declines with age

  • Original Articles
  • Published:
Cancer Immunology, Immunotherapy Aims and scope Submit manuscript

Summary

Lymphocyte-induced angiogenesis factor (LIA) is a product of T lymphocytes which has been shown to stimulate new vessel formation. Because immune senescence most profoundly affects T lymphocyte functions, we suspected that LIA production would decline with age. An assay for angiogenesis stimulated by allogeneic reaction was performed by injecting spleen cells from young or old donor mice into the skin of irradiated allogeneic recipient mice. The spleen cells from young mice induced a significantly greater number of vessels than did cells from older mice. In additional experiments, spleen cells from young and old animals were treated with a monoclonal antibody GK1.5) directed at the L3T4 antigen on murine T helper lymphocytes. Such treatment significantly reduced the new vessel formation induced by young lymphocytes but had no effect on that induced by lymphocytes from old animals. Studies employing indirect immunofluorescence demonstrated that the proportion of L3T4+ cells in the mononuclear fraction of splenocytes was nearly identical in both young and old mice. From these investigations we can conclude that (1) L3T4+ lymphocytes are responsible for LIA production, and (2) production, like that of other T lymphokines, declines with age.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Auerbach R (1981) Angiogenesis-inducing factors: A review. Lymphokines 4:69

    Google Scholar 

  2. Auerbach R, Kubai L, Sidky Y (1976) Angiogenesis induction by tumors, embryoynic tissues, and lymphocytes. Cancer Res 36:3435

    Google Scholar 

  3. Dialynas DP, Quan ZS, Wall KA, Pierres A, Quintans J, Loken MR, Pierres M, Fitch FW (1983) Characterization of the murine T cell surface molecule, designated L3T4, identified by monoclonal antibody GK1.5: Similarity of L3T4 to the human Leu-3/T4 molecule. J Immunol 131:2445

    Google Scholar 

  4. Ershler WB, Gamelli RL, Moore AL, Hacker MP, Blow AJ (1984) Experimental tumors and aging: Local factors that may account for the observed age advantage in the B16 murine melanoma model. Exp Gerontol 19:367

    Google Scholar 

  5. Ershler WB, Moore AL, Shore H, Gamelli RL (1984) Transfer of age-associated restrained tumor growth in mice by old-to-young bone marrow transplantation. Cancer Res 44:5677

    Google Scholar 

  6. Ershler WB, Stewart JA, Hacker MP, Moore AL, Tindle BH (1984) B16 murine melanoma and aging: Slower growth and longer survival in old mice. J Natl Cancer Inst 72:161

    Google Scholar 

  7. Folkman J (1985) Angiogenesis and its inhibitors: In: Important advances in oncology 1985. JB Lippincott Company, Philadelphia, p 42

    Google Scholar 

  8. Folkman J (1985) Tumor angiogenesis: In: Advances in cancer research. New York Academic Press, New York, p 175

    Google Scholar 

  9. Folkman J (1986) How is blood vessel growth regulated in normal and neoplastic tissue? G. H. A. Clowes Memorial Award Lecture. Cancer Res 46:467

    CAS  PubMed  Google Scholar 

  10. Gimbrone MA Jr., Leapman SB, Cotran RS, Folkman J (1972) Tumor dormancy in vivo by prevention of neovascularization. J Exp Med 136:261

    Google Scholar 

  11. Gimbrone MS, Leapman S, Cotran RS, Folkman J (1973) Tumor angiogenesis: Iris neovascularization at a distance from experimental intraocular tumors. J Natl Cancer Inst 50:219

    Google Scholar 

  12. Greenblatt M, Shubik P (1968) Tumor angiogenesis: Trans-filter diffusion studies in the hamster by the transparent chamber technque. J Natl Cancer Inst 41:111

    Google Scholar 

  13. Koch AE, Polverini PJ, Leibovich SJ (1986) Induction of neovascularization by activated human monocytes. J Leuk biol 39:233

    Google Scholar 

  14. Majewski S, Kaminski M, Jablonska S, Szmurlo A, Pawinska M (1985) Angiogenic capability of peripheral blood mononuclear cells in psoriasis. Arch Dermatol 121:1018

    Google Scholar 

  15. Makinodan T, Kay MM (1980) Age influence on the immune system. Adv Immunol 29:287

    Google Scholar 

  16. Moore K, Moore M (1977) Intra-tumour host cells of transplanted rat neoplasms of different immunogenicity. Int J Cancer 19:803

    Google Scholar 

  17. Sidky YA, Auerbach R (1975) Lymphocyte-induced angiogenesis: A quantitative and sensitive assay of the graft-vs.-host reaction. J Exp Med 141:1084

    Google Scholar 

  18. Sidky YA, Auerbach R (1979) Response of the host vascular system to immunocompetent lymphocytes: Effect of preimmunization of donor or host animals. Proc Soc Exp Biol Med 161:174

    Google Scholar 

  19. Weksler ME, Innes JB, Goldstein G (1978) Immunological studies of aging. IV. The contribution of thymic involution to the immune deficiencies of aging mice and reversal with thymopoietin. J Exp Med 148:996

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported by NIH grant AG 00332 and VA Merit Award (WBE)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hadar, E.J., Ershler, W.B., Kreisle, R.A. et al. Lymphocyte-induced angiogenesis factor is produced by L3T4+ murine T lymphocytes, and its production declines with age. Cancer Immunol Immunother 26, 31–34 (1988). https://doi.org/10.1007/BF00199844

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00199844

Keywords

Navigation