Decellularised extracellular matrix-derived peptides from neural retina and retinal pigment epithelium enhance the expression of synaptic markers and light responsiveness of human pluripotent stem cell derived retinal organoids

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DOI

  • Birthe Dorgau
  • Majed Felemban
  • Gerrit Hilgen
  • Martin Kiening
  • Darin Zerti
  • Nicola Claire Hunt
  • Mary Doherty
  • Phil Whitfield
  • Dean Hallam
  • Kathryn White
  • Yuchun Ding
  • Natalio Krasnogor
  • Jumana Al-aama
  • Hani Z. Asfour
  • Evelyne Sernagor
  • Majlinda Lako

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Original languageEnglish
Pages (from-to)63-75
Number of pages13
JournalBiomaterials
Volume199
Early online date22 Jan 2019
DOIs
Publication statusPublished - Apr 2019

    Research areas

  • Decellularisation, Extracellular matrix, RPE, Neural retina, Retinal organoids, Human pluripotent stem cells

Abstract

Tissue specific extracellular matrices (ECM) provide structural support and enable access to molecular signals and metabolites, which are essential for directing stem cell renewal and differentiation. To mimic this phenomenon in vitro, tissue decellularisation approaches have been developed, resulting in the generation of natural ECM scaffolds that have comparable physical and biochemical properties of the natural tissues and are currently gaining traction in tissue engineering and regenerative therapies due to the ease of standardised production, and constant availability. In this manuscript we report the successful generation of decellularised ECM-derived peptides from neural retina (decel NR) and retinal pigment epithelium (decel RPE), and their impact on differentiation of human pluripotent stem cells (hPSCs) to retinal organoids. We show that culture media supplementation with decel RPE and RPE-conditioned media (CM RPE) significantly increases the generation of rod photoreceptors, whilst addition of decel NR and decel RPE significantly enhances ribbon synapse marker expression and the light responsiveness of retinal organoids. Photoreceptor maturation, formation of correct synapses between retinal cells and recording of robust light responses from hPSC-derived retinal organoids remain unresolved challenges for the field of regenerative medicine. Enhanced rod photoreceptor differentiation, synaptogenesis and light response in response to addition of decellularised matrices from RPE and neural retina as shown herein provide a novel and substantial advance in generation of retinal organoids for drug screening, tissue engineering and regenerative medicine.

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