4.6 Article

Decellularized Avian Cartilage, a Promising Alternative for Human Cartilage Tissue Regeneration

Journal

MATERIALS
Volume 15, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/ma15051974

Keywords

chondrocytes; extracellular matrix; cartilage; decellularization; scaffold

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Articular cartilage defects are common and contribute to poor quality of life and osteoarthritis. Tissue engineering, using decellularized scaffolds, shows promise for regenerating damaged cartilage. In this study, avian articular cartilage scaffolds reseeded with human chondrocytes were found to support cell survival, proliferation, and interaction. The decellularized scaffolds had a porous architecture and mechanical properties similar to native cartilage. These findings suggest that decellularized scaffolds are suitable for cartilage regeneration.
Articular cartilage defects, and subsequent degeneration, are prevalent and account for the poor quality of life of most elderly persons; they are also one of the main predisposing factors to osteoarthritis. Articular cartilage is an avascular tissue and, thus, has limited capacity for healing and self-repair. Damage to the articular cartilage by trauma or pathological causes is irreversible. Many approaches to repair cartilage have been attempted with some potential; however, there is no consensus on any ideal therapy. Tissue engineering holds promise as an approach to regenerate damaged cartilage. Since cell adhesion is a critical step in tissue engineering, providing a 3D microenvironment that recapitulates the cartilage tissue is vital to inducing cartilage regeneration. Decellularized materials have emerged as promising scaffolds for tissue engineering, since this procedure produces scaffolds from native tissues that possess structural and chemical natures that are mimetic of the extracellular matrix (ECM) of the native tissue. In this work, we present, for the first time, a study of decellularized scaffolds, produced from avian articular cartilage (extracted from Gallus Gallus domesticus), reseeded with human chondrocytes, and we demonstrate for the first time that human chondrocytes survived, proliferated and interacted with the scaffolds. Morphological studies of the decellularized scaffolds revealed an interconnected, porous architecture, ideal for cell growth. Mechanical characterization showed that the decellularized scaffolds registered stiffness comparable to the native cartilage tissues. Cell growth inhibition and immunocytochemical analyses showed that the decellularized scaffolds are suitable for cartilage regeneration.

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