Suitability of ex vivo-expanded microtic perichondrocytes for auricular reconstruction

Tissue engineering (TE) techniques offer solutions for tissue regeneration but require large quantities of cells. For microtia patients, TE methods represent a unique opportunity for therapies with low donor-site morbidity and reliance on the surgeon’s individual expertise. Microtia-derived chondroc...

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Hauptverfasser: Jakob, Yvonne (VerfasserIn) , Kern, Johann (VerfasserIn) , Gvaramia, David (VerfasserIn) , Fisch, Philipp (VerfasserIn) , Magritz, Ralph (VerfasserIn) , Reutter, Sven (VerfasserIn) , Rotter, Nicole (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 12 January 2024
In: Cells
Year: 2024, Jahrgang: 13, Heft: 2, Pages: 1-19
ISSN:2073-4409
DOI:10.3390/cells13020141
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.3390/cells13020141
Verlag, kostenfrei, Volltext: https://www.mdpi.com/2073-4409/13/2/141
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Verfasserangaben:Yvonne Jakob, Johann Kern, David Gvaramia, Philipp Fisch, Ralph Magritz, Sven Reutter and Nicole Rotter

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520 |a Tissue engineering (TE) techniques offer solutions for tissue regeneration but require large quantities of cells. For microtia patients, TE methods represent a unique opportunity for therapies with low donor-site morbidity and reliance on the surgeon’s individual expertise. Microtia-derived chondrocytes and perichondrocytes are considered a valuable cell source for autologous reconstruction of the pinna. The aim of this study was to investigate the suitability of perichondrocytes from microtia patients for autologous reconstruction in comparison to healthy perichondrocytes and microtia chondrocytes. Perichondrocytes were isolated via two different methods: explant culture and enzymatic digestion. The isolated cells were analyzed in vitro for their chondrogenic cell properties. We examined migration activity, colony-forming ability, expression of mesenchymal stem cell markers, and gene expression profile. We found that microtic perichondrocytes exhibit similar chondrogenic properties compared to chondrocytes in vitro. We investigated the behavior in three-dimensional cell cultures (spheroids and scaffold-based 3D cell cultures) and assessed the expression of cartilage-specific proteins via immunohistochemistry, e.g., collagen II, which was detected in all samples. Our results show that perichondrocytes from microtia patients are comparable to healthy perichondrocytes and chondrocytes in terms of chondrogenic cell properties and could therefore be a promising cell source for auricular reconstruction. 
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