June 1997
Volume 38, Issue 7
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Articles  |   June 1997
Repair phenotype in corneal fibroblasts is controlled by an interleukin-1 alpha autocrine feedback loop.
Author Affiliations
  • J A West-Mays
    Vision Research Laboratories, New England Medical Center, Boston, MA 02111, USA.
  • P M Sadow
    Vision Research Laboratories, New England Medical Center, Boston, MA 02111, USA.
  • T W Tobin
    Vision Research Laboratories, New England Medical Center, Boston, MA 02111, USA.
  • K J Strissel
    Vision Research Laboratories, New England Medical Center, Boston, MA 02111, USA.
  • C Cintron
    Vision Research Laboratories, New England Medical Center, Boston, MA 02111, USA.
  • M E Fini
    Vision Research Laboratories, New England Medical Center, Boston, MA 02111, USA.
Investigative Ophthalmology & Visual Science June 1997, Vol.38, 1367-1379. doi:
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      J A West-Mays, P M Sadow, T W Tobin, K J Strissel, C Cintron, M E Fini; Repair phenotype in corneal fibroblasts is controlled by an interleukin-1 alpha autocrine feedback loop.. Invest. Ophthalmol. Vis. Sci. 1997;38(7):1367-1379.

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Abstract

PURPOSE: To explore the role of autocrine interleukin-1 alpha (IL-1 alpha) as a central regulator of the repair phenotype in corneal fibroblasts. METHODS: Disruption of the actin cytoskeleton with cytochalasin B (CB), which mimics changes in shape that occur in repair tissues, was used to stimulate repair gene expression in early-passage fibroblasts. Changes in expression of IL-1 alpha, IL-8, collagenase, and ENA-78 were determined by Northern blot analysis, radioimmunoassay, and an enzyme-amplified sensitivity immunoassay (EASIA). Expression of repair genes was also examined in repair fibroblasts, isolated from healing, penetrating keratectomy wounds in rabbits. RESULTS: Blocking IL-1 alpha activity prevented both constitutive and stimulated increases in synthesis of IL-8 and collagenase in early-passage cultures of corneal fibroblasts, demonstrating the role of IL-1 alpha as a necessary intermediate for expression of these genes. Evidence is also presented that the IL-1 alpha autocrine controls expression of an IL-8 related factor, ENA-78. Unlike early-passage fibroblasts, fibroblasts freshly isolated from the uninjured cornea did not express IL-1 alpha. However, fibroblasts freshly isolated from remodeling corneal repair tissue 3 weeks after injury were found to express substantial levels of IL-1 alpha, regulated through an autocrine feedback loop. Neutralization experiments demonstrated that the IL-1 alpha autocrine is largely responsible for controlling both collagenase and IL-8 synthesis in repair fibroblasts, as it is in early-passage fibroblasts. CONCLUSIONS: These findings provide evidence that activation of an autocrine IL-1 alpha feedback loop is an important mechanism by which fibroblasts adopt a repair phenotype during remodeling of the cornea.

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