Characterization of Danio Rerio Retinal Regeneration and the Role of TNFα, Stat3, and Ascl1a During the Initiation of MÌ_ller Glia Proliferation

Doctoral Dissertation


Zebrafish is an excellent model organism to study the molecular basis of retinal regeneration. Damage-induced apoptosis of retinal neurons in adult zebrafish stimulates MÌ_ller glia within the inner nuclear layer to dedifferentiate and divide giving rise to undifferentiated transiently amplifying multipotent neuronal progenitor daughter cells. These cells continue to proliferate and migrate to the damaged retinal layer where they differentiate into functional and integrated retinal neurons. The mechanisms in which MÌ_ller glia are induced to divide by the apoptotic neurons during the initiation of regeneration are unknown.

Following retinal damage, the expression of transcription factors Signal transducer and activator of transcription 3 (Stat3) and Achaete-scute complex-like 1a (Ascl1a) are upregulated in MÌ_ller glia and are each required for maximal MÌ_ller glia proliferation following retinal damage. To examine the requirement of each of these factors for regeneration and their hierarchal relationship, morpholino-mediated knockdowns were performed. This analysis revealed a complex signaling cascade involving three separate populations of MÌ_ller glia that have differential requirements for the expression of Stat3, Ascl1a and proliferation (Nelson et al., in press).

To examine the mechanism in which MÌ_ller glia are signaled to divide, retinal lysates were collected at the peak of photoreceptor apoptosis, homogenized and injected into the intravitreal space of undamaged eyes. The light-damaged retinal homogenates stimulated MÌ_ller glia proliferation, which demonstrated that a MÌ_ller glia proliferation-stimulating factor was present during the peak of photoreceptor apoptosis.

To identify candidate protein signaling pathways that could be responsible for the initiation of MÌ_ller glia proliferation, I performed a MALDI-TOF mass spectrometry proteomic analysis comparing proteins of undamaged retinas to those isolated during the peak of light-induced photoreceptor apoptosis. Tumor necrosis factor α (TNFα) signaling proteins were increased in expression in the light-damaged retinas. TNFα expression was increased by apoptotic photoreceptors and later in MÌ_ller glia. Knockdown of TNFα significantly decreased the expression of Ascl1a and Stat3 and significantly reduced the number of MÌ_ller glia stimulated to reenter the cell cycle, but did not affect levels of photoreceptor death. This study identifies the TNFα signaling pathway as a novel participant that is induced by retinal damage which acts upstream of Ascl1a and Stat3 during Danio rerio photoreceptor regeneration.


Attribute NameValues
  • etd-08262012-102953

Author Craig Michael Nelson
Advisor David Hyde
Contributor David Hyde, Committee Chair
Contributor Lei Li, Committee Member
Contributor Joseph OTousa, Committee Member
Contributor Robert Schulz, Committee Member
Degree Level Doctoral Dissertation
Degree Discipline Biological Sciences
Degree Name PhD
Defense Date
  • 2012-08-23

Submission Date 2012-08-26
  • United States of America

  • regeneration

  • Tumor necrosis factor-alpha

  • zebrafish

  • neuroscience

  • ascl1a

  • stat3

  • University of Notre Dame

  • English

Record Visibility Public
Content License
  • All rights reserved

Departments and Units


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