Suitability of Ex Vivo-Expanded Microtic Perichondrocytes for Auricular Reconstruction

被引:0
作者
Jakob, Yvonne [1 ]
Kern, Johann [1 ]
Gvaramia, David [1 ]
Fisch, Philipp [2 ]
Magritz, Ralph [3 ]
Reutter, Sven [1 ]
Rotter, Nicole [1 ]
机构
[1] Heidelberg Univ, Med Fac Mannheim, Dept Otorhinolaryngol Head & Neck Surg, Theodor Kutzer Ufer 1-3, D-68167 Mannheim, Germany
[2] Swiss Fed Inst Technol, Dept Hlth Sci & Technol, Tissue Engn & Biofabricat Lab, Otto Stern Weg 7, CH-8093 Zurich, Switzerland
[3] Oberhavel Kliniken GmbH, Clin Otorhinolaryngol, Klin Henningsdorf, Marwitzer Str 91, D-16761 Hennigsdorf, Germany
关键词
perichondrocytes; microtia; tissue engineering; auricular reconstruction; 3D cell cultures; spheroids; COSTAL CARTILAGE FRAMEWORK; POROUS TISSUE BIOSCAFFOLDS; HUMAN ELASTIC CARTILAGE; EAR-SHAPED CARTILAGE; PROGENITOR CELLS; FORMING CAPACITY; STEM-CELL; CHONDROCYTES; AURICLE; REGENERATION;
D O I
10.3390/cells13020141
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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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页数:19
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