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Polarized, Cobblestone, Human Retinal Pigment Epithelial Cell Maturation on a Synthetic PEG Matrix

  • Yangzi Tian
  • , Michael R. Zonca
  • , Joseph Imbrogno
  • , Andrea M. Unser
  • , Lauren Sfakis
  • , Sally Temple
  • , Georges Belfort
  • , Yubing Xie
  • SUNY Polytechnic Institute
  • Rensselaer Polytechnic Institute
  • Neural Stem Cell Institute

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Cell attachment is essential for the growth and polarization of retinal pigment epithelial (RPE) cells. Currently, surface coatings derived from biological proteins are used as the gold standard for cell culture. However, downstream processing and purification of these biological products can be cumbersome and expensive. In this study, we constructed a library of chemically modified nanofibers to mimic the Bruch's membrane of the retinal pigment epithelium. Using atmospheric-pressure plasma-induced graft polymerization with a high-Throughput screening platform to modify the nanofibers, we identified three polyethylene glycol (PEG)-grafted nanofiber surfaces (PEG methyl ether methacrylate, n = 4, 8, and 45) from a library of 62 different surfaces as favorable for RPE cell attachment, proliferation, and maturation in vitro with cobblestone morphology. Compared with the biologically derived culture matrices such as vitronectin-based peptide Synthemax, our newly discovered synthetic PEG surfaces exhibit similar growth and polarization of retinal pigment epithelial (RPE) cells. However, they are chemically defined, are easy to synthesize on a large scale, are cost-effective, are stable with long-Term storage capability, and provide a more physiologically accurate environment for RPE cell culture. To our knowledge, no one has reported that PEG derivatives directly support attachment and growth of RPE cells with cobblestone morphology. This study offers a unique PEG-modified 3D cell culture system that supports RPE proliferation, differentiation, and maturation with cobblestone morphology, providing a new avenue for RPE cell culture, disease modeling, and cell replacement therapy.

Original languageEnglish
Pages (from-to)890-902
Number of pages13
JournalACS Biomaterials Science and Engineering
Volume3
Issue number6
DOIs
StatePublished - Jun 12 2017

Keywords

  • PEG
  • RPE
  • high throughput screening
  • nanofibrous matrix
  • stem cells
  • surface chemistry

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