Activation of Wnt/β-catenin signaling in Muller glia protects photoreceptors in a mouse model of inherited retinal degeneration

Amit K. Patel, Krishna Surapaneni, Hyun Yi, Rei E.I. Nakamura, Sapir Z. Karli, Sarah Syeda, Tinthu Lee, Abigail S. Hackam

Research output: Contribution to journalArticle

22 Scopus citations

Abstract

The canonical Wnt/β-catenin ("Wnt") pathway is an essential signaling cascade in the embryonic central nervous system (CNS) that regulates neuronal differentiation and survival. Loss of Wnt signaling in developing and adult tissue has been implicated in numerous CNS diseases, but the precise role of Wnt in regulating neuronal survival, and how its absence could lead to disease, is not understood. In this study, we investigated the effect of Wnt activation on neuronal survival in the adult retina, and identified cellular and molecular mediators. Pan-retinal Wnt signaling activation using Wnt3a induced functional and morphological rescue of photoreceptor neurons in the rd10 mouse model of retinal degeneration. Furthermore, Wnt activation using constitutively active β-catenin specifically targeted to Muller glia increased photoreceptor survival and reduced markers of glial and neuronal remodeling. Wnt-induced photoreceptor protection was associated with elevated levels of the prosurvival protein Stat3, and was reduced by shRNA-mediated knock-down of Stat3, indicating cross-talk between survival pathways. Therefore, these data increase our understanding of the role of Wnt signaling in the retina, and identify radial Muller glia as important cellular mediators of Wnt activity.

Original languageEnglish (US)
Pages (from-to)1-12
Number of pages12
JournalNeuropharmacology
Volume91
DOIs
StatePublished - Apr 2015

Keywords

  • Muller glia
  • Neuroprotection
  • Retina
  • Stat3
  • Wnt

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Pharmacology

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