EMBO Molecular Medicine (Apr 2022)

Early disruption of photoreceptor cell architecture and loss of vision in a humanized pig model of usher syndromes

  • Sophia Grotz,
  • Jessica Schäfer,
  • Kirsten A Wunderlich,
  • Zdenka Ellederova,
  • Hannah Auch,
  • Andrea Bähr,
  • Petra Runa‐Vochozkova,
  • Janet Fadl,
  • Vanessa Arnold,
  • Taras Ardan,
  • Miroslav Veith,
  • Gianluca Santamaria,
  • Georg Dhom,
  • Wolfgang Hitzl,
  • Barbara Kessler,
  • Christian Eckardt,
  • Joshua Klein,
  • Anna Brymova,
  • Joshua Linnert,
  • Mayuko Kurome,
  • Valeri Zakharchenko,
  • Andrea Fischer,
  • Andreas Blutke,
  • Anna Döring,
  • Stepanka Suchankova,
  • Jiri Popelar,
  • Eduardo Rodríguez‐Bocanegra,
  • Julia Dlugaiczyk,
  • Hans Straka,
  • Helen May‐Simera,
  • Weiwei Wang,
  • Karl‐Ludwig Laugwitz,
  • Luk H Vandenberghe,
  • Eckhard Wolf,
  • Kerstin Nagel‐Wolfrum,
  • Tobias Peters,
  • Jan Motlik,
  • M Dominik Fischer,
  • Uwe Wolfrum,
  • Nikolai Klymiuk

DOI
https://doi.org/10.15252/emmm.202114817
Journal volume & issue
Vol. 14, no. 4
pp. n/a – n/a

Abstract

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Abstract Usher syndrome (USH) is the most common form of monogenic deaf‐blindness. Loss of vision is untreatable and there are no suitable animal models for testing therapeutic strategies of the ocular constituent of USH, so far. By introducing a human mutation into the harmonin‐encoding USH1C gene in pigs, we generated the first translational animal model for USH type 1 with characteristic hearing defect, vestibular dysfunction, and visual impairment. Changes in photoreceptor architecture, quantitative motion analysis, and electroretinography were characteristics of the reduced retinal virtue in USH1C pigs. Fibroblasts from USH1C pigs or USH1C patients showed significantly elongated primary cilia, confirming USH as a true and general ciliopathy. Primary cells also proved their capacity for assessing the therapeutic potential of CRISPR/Cas‐mediated gene repair or gene therapy in vitro. AAV‐based delivery of harmonin into the eye of USH1C pigs indicated therapeutic efficacy in vivo.

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