July 2018
Volume 59, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2018
Expression of an Anti-Inflammatory Peptide using a Minicircle-Plasmid delivery system in RPE Cell Culture
Author Affiliations & Notes
  • Max Brinkmann
    Department of Ophthalmology, University of Luebeck, Luebeck, Germany
  • Maximilian Kurz
    Department of Ophthalmology, University of Luebeck, Luebeck, Germany
  • Markus Mandl
    Institute of Integrative and Experimental Genomics, University of Lübeck, Luebeck, Germany
  • Zouhair Aherrahrou
    Institute of Integrative and Experimental Genomics, University of Lübeck, Luebeck, Germany
  • Armin Mohi
    Department of Ophthalmology, University of Luebeck, Luebeck, Germany
  • Salvatore Grisanti
    Department of Ophthalmology, University of Luebeck, Luebeck, Germany
  • Mahdy Ranjbar
    Department of Ophthalmology, University of Luebeck, Luebeck, Germany
  • Martin Rudolf
    Department of Ophthalmology, University of Luebeck, Luebeck, Germany
  • Footnotes
    Commercial Relationships   Max Brinkmann, None; Maximilian Kurz, None; Markus Mandl, None; Zouhair Aherrahrou, None; Armin Mohi, None; Salvatore Grisanti, None; Mahdy Ranjbar, None; Martin Rudolf, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science July 2018, Vol.59, 73. doi:
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      Max Brinkmann, Maximilian Kurz, Markus Mandl, Zouhair Aherrahrou, Armin Mohi, Salvatore Grisanti, Mahdy Ranjbar, Martin Rudolf; Expression of an Anti-Inflammatory Peptide using a Minicircle-Plasmid delivery system in RPE Cell Culture. Invest. Ophthalmol. Vis. Sci. 2018;59(9):73.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Several retinal diseases are marked by chronically increased local inflammation in which the retinal pigment epithelium (RPE) is a main responder. To make stressed RPE cells more resistant to local inflammation we want to transfect them with minicircles, which are small circular plasmid derivates free of all prokaryotic DNA elements. Encoded is an 18 amino acids long peptide which is able to scavenge pro-inflammatory oxidized phospholipids thereby regulating RPE environment. Here we present the RPE-transfection with minicircles and peptide detection.

Methods : Primary human RPE- cells and ARPE-19 cells were cultured and were transfected with minicircles. Our first minicirlce (MC1) encodes for the active peptide as well for green fluorescent protein (GFP). Both sequences are separated by an internal ribosome entry site (IRES) and translated independently from the same mRNA. Our control minicircle (MC2) encodes no peptide but only a red fluorescent protein (RFP) to monitor transfection efficiency. Finally, GFP and RFP expression is analysed by fluorescence microscopy.

Results : Both GFP and RFP are already detectable in RPE cells after 24h by fluorescence microscopy after MC transfer. The signal rose after 48h. Because GFP and the active scavenging peptide are transcribed on the same mRNA but translated as two independent molecules, the fluorescent marker is an indicator for expression efficiency.

Conclusions : The presented results show the feasibility to transfect human RPE cells with minicircle plasmids. A polyclonal antibody raised against the peptide will be used in future experiments for direct detection. In order to complement this study a very sensitive approach using mass spectrometry is planned.


This is an abstract that was submitted for the 2018 ARVO Annual Meeting, held in Honolulu, Hawaii, April 29 - May 3, 2018.

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