<resource xmlns:datacite="http://datacite.org/schema/kernel-4">
<creators>
<creator>
<creatorName>Csukovich, Georg (University of Veterinary Medicine Vienna)</creatorName>
<givenName>Georg</givenName>
<familyName>Csukovich</familyName>
</creator>
<creator>
<creatorName>Burgener, Iwan Anton (University of Veterinary Medicine Vienna)</creatorName>
<givenName>Iwan Anton</givenName>
<familyName>Burgener</familyName>
</creator>
<creator>
<creatorName>Pratscher, Barbara (University of Veterinary Medicine Vienna)</creatorName>
<givenName>Barbara</givenName>
<familyName>Pratscher</familyName>
</creator>
<creator>
<creatorName>Huainig, Janina (University of Veterinary Medicine Vienna)</creatorName>
<givenName>Janina</givenName>
<familyName>Huainig</familyName>
</creator>
<creator>
<creatorName>Troester, Selina (University of Veterinary Medicine Vienna)</creatorName>
<givenName>Selina</givenName>
<familyName>Troester</familyName>
</creator>
</creators>
<titles>
<title>The Intricacies of Inflammatory Bowel Disease: A Preliminary Study of Redox Biology in Intestinal Organoids</title>
</titles>
<publisher>MDPI</publisher>
<publicationYear>2023</publicationYear>
<descriptions>
<description descriptionType="Other">We evaluated the redox status, precisely glutathione levels, which have a major impact in cellular detoxification and antioxidant defence in IBD-derived and healthy intestinal organoids. Therefore, we wanted to explore the differences in terms of their redox balance and mitochondrial fitness. To this end, we introduced a Grx1-roGFP2 construct into the organoids by lentiviral transduction before performing a stress assay by treating the organoids with hydrogen peroxide and examined the GSH/GSSG ratio using confocal imaging. Using ratio imaging, we could detect statistically significant differences between healthy and IBD-derived samples. To gain more insight, we also performed a GSH/GSSG assay, which directly measured glutathione levels. This analysis revealed that both organoid lines had higher levels of oxidized glutathione due to the stress treatment demonstrated by a lower GSH/GSSG ratio compared to the untreated control. Nevertheless, the results showed no significant difference between healthy and IBD-derived organoids. We further challenged organoids with hydrogen peroxide after incubation with MitoTracker® to see if mitochondrial fitness might be different in IBD-derived organoids. However, these results were also very comparable. In summary, our preliminary findings indicate that both organoid lines demonstrate a well-functioning system in terms of analysis but show no clear difference between healthy and IBD-derived samples.</description>
</descriptions>
<resourceType resourceTypeGeneral="Text">PDFDocument</resourceType>
<language>en</language>
<dates>
<date dateType="Created">2024-03-05T09:14:13.960Z</date>
</dates>
<subjects>
<subject>intestinal organoid; redox biology; IBD; glutathione; oxidative stress; ROS; redox imaging</subject>
</subjects>
<sizes>
<size>447854 b</size>
</sizes>
<formats>
<format>application/pdf</format>
</formats>
<rightsList>
<rights rightsURI="http://creativecommons.org/licenses/by/4.0/">CC BY 4.0 International</rights>
</rightsList>
</resource>
