August 1974
Volume 13, Issue 8
Free
Articles  |   August 1974
Induction of Endothelial Cell Proliferation in Rat Retinal Venules by Chemical and Indirect Physical Trauma
Author Affiliations
  • CLARK W. DEEM
    Department of Ophthalmology, University of Washington School of Medicine, Seattle, Wash. 98195
  • SIDNEY FUTTERMAN
    Department of Ophthalmology, University of Washington School of Medicine, Seattle, Wash. 98195
  • ROBERT E. KALINA
    Department of Ophthalmology, University of Washington School of Medicine, Seattle, Wash. 98195
Investigative Ophthalmology & Visual Science August 1974, Vol.13, 580-585. doi:
  • Views
  • PDF
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      CLARK W. DEEM, SIDNEY FUTTERMAN, ROBERT E. KALINA; Induction of Endothelial Cell Proliferation in Rat Retinal Venules by Chemical and Indirect Physical Trauma. Invest. Ophthalmol. Vis. Sci. 1974;13(8):580-585.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
This content is PDF only. Please click on the PDF icon to access.
Abstract

The capacity of retinal vessels to incorporate tritiated thymidine was studied in normal rats and in rats previously exposed to ocular trauma for the purpose of developing a model for the study of neovascularization in the retina. Needle puncture of the lens capsule caused intraocular inflammation and a 30- to 70-fold increase in the number of venular endothelial cells which incorporated tritiated thymidine. The time course of entry of venular endothelial cells into the S-phase of the cell cycle was studied following lens injury. An increase in the frequency of labeled cells was first detected six hours after lens injury and two hours after the appearance of leukocytes within the lumen of vessels. The number of endothelial cells in S-phase peaked sharply at eight hours and again at 40 hours following lens injury, indicating cell synchrony and a 32-hour duration for the complete cell cycle.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×