Skip to main content
Log in

In vivo observations on experimental corneal neovascularization with a newly developed macroscope

  • Laboratory Investigations
  • Published:
Graefe's Archive for Clinical and Experimental Ophthalmology Aims and scope Submit manuscript

Abstract

The process of corneal neovascularization induced by alkali burns was periodically observed with a newly developed macroscope. The central corneas were burned using filter discs measuring 6 mm in diameter that had been immersed in 1 N NaOH. At 0, 1, 3 and 7 days and at 2, 3 and 4 weeks after injury, the corneas were observed with the macroscope and then examined histologically. At 1 day post-burn, the limbal vascular plexus was engorged but no new vessel formation was detected. By 3 days, many vascular sprouts had arisen from the limbal vascular arcade. At 7 days, the vascular sprouts grew and became fine new vessels. At 2 weeks, the new vessels lengthened further to the central cornea. At 3 weeks, trunk vessels extended and branched like a vascular tree. Blood in the trunk vessels appeared to flow slowly to and fro. The ends of the vessels swelled in a fusiform shape on the application of slight pressure of the macroscope probe. Histological examination revealed that the ends of the vessels consisted of single vascular endothelial cells and the trunk vessels were covered by pericytes. By 4 weeks, the branch vessels around the burned lesion had degenerated and collapsed. Thus, our in vivo study using the new macroscope not only clarified the process of corneal neovascularization from the early to the regressive phases but also provided some valuable new information.

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. Beck DW, Hart MN, Cancilla PA (1983) The role of the macrophage in microvascular regeneration following brain injury. J Neuropathol Exp Neurol 42:601–612

    Google Scholar 

  2. BenEzra D (1978) Mediators of immunological reactions: function as inducers of neovascularization. Metab Ophthalmol 2:339–341

    Google Scholar 

  3. Burger PC, Chandler DB, Klintworth GK (1983) Corneal neovascularization as studied by scanning electron microscopy of vascular casts. Lab Invest 48:169–180

    Google Scholar 

  4. Cogan DG (1949) Vascularization of the cornea: its experimental induction by small lesions and a new theory of its pathogenesis. Arch Ophthalmol 41:406–416

    Google Scholar 

  5. Epstein RJ, Hughes WF (1981) Lymphocyte-induced corneal neovascularization: a morphological assessment. Invest Ophthalmol Vis Sci 21:87–94

    Google Scholar 

  6. Folkman J, Merler E, Abenathy C, Willams G (1971) Isolation of a tumor factor responsible for angiogenesis. J Exp Med 133:275–288

    Google Scholar 

  7. Fromer CH, Klintworth GK (1975) An evaluation of the role of leukocytes in the pathogenesis of experimentally induced corneal neovascularization: I. Comparison of experimental models of corneal vascularization. Am J Pathol 79:537–550

    Google Scholar 

  8. Fromer CH, Klintworth GK (1976) An evaluation of the role of leukocytes in the pathogenesis of experimentally induced corneal vascularization: III. Studies related to vasoproliferative capability of polymorphonuclear leukocytes and lymphocytes. Am J Pathol 82:157–166

    Google Scholar 

  9. Klintworth GK (1977) The contribution of morphology to our understanding of the pathogenesis of experimentally produced corneal neovascularization. Invest Ophthalmol 16:281–285

    Google Scholar 

  10. Klintworth GK, Burger PC (1983) Neovascularization of the cornea: current concepts of its pathogenesis. Am J Pathol Int Ophthalmol Clin 23:27–39

    Google Scholar 

  11. Lutty GA, Lui SH, Prendergast RA (1983) Angiogenic lym-phokines of activated T-cell origin. Invest Ophthalmol Vis Sci 24:1595–1601

    Google Scholar 

  12. Matsuhashi K (1962) Experimental study on the corneal neovascularization: II. Electron microscope observation on the corneal vascularization. Acta Soc Ophthalmol Jpn 66:942–952

    Google Scholar 

  13. Maurice DM, Zauberman H, Michaelson IC (1966) The stimulus to neovascularization in the cornea. Exp Eye Res 5:168–184

    Google Scholar 

  14. McCracken JS, Burger PC, Klintworth GK (1979) Morphologic observations on experimental corneal vascularization in the rat. Lab Invest 41:519–530

    Google Scholar 

  15. Ormerod LD, Abelson MB, Kenyon KR (1989) Standard models of corneal injury using alkali-immersed filter discs. Invest Ophthalmol Vis Sci 30:2148–2153

    Google Scholar 

  16. Polverini PJ, Cotran RS, Gimborne MA Jr, Unanue ER (1977) Activated macrophages induce vascular proliferation. Nature 269:804–806

    Google Scholar 

  17. Schanzlin DJ, Cyr RJ, Friedlaender MH (1983) Histopathology of corneal vascularization. Arch Ophthalmol 101:472–474

    Google Scholar 

  18. Sholley MM, Ferguson GP, Seibel HR, Montour JL, Wilson J (1984) Mechanisms of neovascularization: vascular sprouting can occur without proliferation of endothelial cells. Lab Invest 51:624–634

    Google Scholar 

  19. 19.Sugiura S, Matsuda H (1969) Electron microscopic studies on the corneal neovascularization. Acta Soc Ophthalmol Jpn 73:1208–1221

    Google Scholar 

  20. Yamagami I (1969) Electron microscopic studies of the cornea: I. The mechanism of experimental new vessels formation. Acta Soc Ophthalmol Jpn 73:1222–1242

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hayashi, K., Ishibashi, T. In vivo observations on experimental corneal neovascularization with a newly developed macroscope. Graefe's Arch Clin Exp Ophthalmol 229, 473–479 (1991). https://doi.org/10.1007/BF00166313

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00166313

Keywords

Navigation