Volume 112, Issue 6 pp. 1050-1055
Article

Tissue-Engineered Cartilage on Biodegradable Macroporous Scaffolds: Cell Shape and Phenotypic Expression

Chung-Hwan Baek MD

Corresponding Author

Chung-Hwan Baek MD

Department of Otorhinolaryngology—Head and Neck Surgery, Sungkyunkwan University School of Medicine, Seoul, Korea.

Chung-Hwan Baek, MD, Department of Otorhinolaryngology—Head and Neck Surgery, Sungkyunkwan University School of Medicine, Samsung Medical Center, 50 Ilwon-dong, Kangnam-gu, Seoul, 135-710, Korea.Search for more papers by this author
Jong-Chan Lee MD

Jong-Chan Lee MD

Department of Otorhinolaryngology—Head and Neck Surgery, Sungkyunkwan University School of Medicine, Seoul, Korea.

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Yong-Gi Jung MD

Yong-Gi Jung MD

Department of Otorhinolaryngology—Head and Neck Surgery, Sungkyunkwan University School of Medicine, Seoul, Korea.

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Ye-Jeung Ko MS

Ye-Jeung Ko MS

Samsung Medical Center, Seoul, Korea

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Jun Jin Yoon MS

Jun Jin Yoon MS

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Taejon, Korea.

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Tae Gwan Park PhD

Tae Gwan Park PhD

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Taejon, Korea.

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First published: 02 January 2009
Citations: 22

Supported by a grant from Samsung Biomedical Research Institute.

Abstract

Objective The purpose of the study was to establish in vitro culture of chondrocytes on biodegradable, poly(D,L-lactic-co-glycolic acid) [PLGA] scaffolds.

Study Design Laboratory experiment using cartilage of rat rib and biodegradable scaffolds.

Methods Chondrocytes were cultured on a poly-hydroxyethyl methacrylate (poly-HEMA)–coated dish, proliferated, and transferred into the PLGA scaffolds. Phenotypic expression of cells was examined according to the condition of poly-HEMA coating. Morphological, biochemical, and immunohistochemical characteristics of cells cultured within PLGA scaffolds were also examined.

Results Chondrocytes cultured on a poly-HEMA–coated dish aggregated into distinct nodules containing large clusters of spherical cells and showed cartilage-specific phenotype, collagen type II. The results of immunostaining and reverse transcriptase–polymerase chain reaction of cells cultured within PLGA scaffolds showed cartilage-specific morphological appearance and structural characteristics such as lacunae and expression of collagen type II.

Conclusion The chondrocytes cultured on a poly-HEMA–coated dish and PLGA scaffolds showed chondrocyte-specific phenotypes and morphological appearance.

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