Morphological characteristics on a Scanning Electron Microscope of generated hyaline cartilage tissue from adipose mesenchymal stem cells, on Polycaprolactone scaffolds
Cartilage regeneration is of great interest to the medical community, given the prevalence of osteocartilage defects in the population coupled with the tissue’s low intrinsic self-repair potential. A recently new FDA approved biomaterial and 3D-printing technology provided us the opportunity to fabricate tailor made scaffolds. We used collagen coated and uncoated scaffolds to develop hyaline cartilage from adipose mesenchymal stem cells (ADMSCs). The aim of this study is to present the scaffolds’ morphological characteristics, as observed on a Scanning Electron Microscope (SEM) of generated cartilage tissue and to compare the two types of scaffolds. Cylindrical shaped PCL scaffolds, 10mm in diameter, were fabricated. ADMSCs were harvested and were cultivated on PCL scaffolds. Half of the scaffolds were treated with collagen I by coating. After 26 days in culture, the scaffolds were examined by SEM. Visualization was succeeded on the top and bottom surfaces and on the cross sections of each scaffold. At day 26, scaffolds revealed extensive colonization and viability of ADMSCs, with concurrent depositions of extracellular matrix. SEM images show that surfaces were covered with a significant amount of material with a glossy, transparent appearance, indicating the development of regenerated cartilage, more apparent on the coated scaffolds. Cultured cells demonstrated aligned direction on the scaffolds' fibers and the ECM that was produced connected the pores of the scaffolds by building apparent bridges between them. The penetration of cells was limited in the coated scaffold. We used 3D printing technology for PCL scaffold production, towards a cartilaginous implant development. SEM images provide us visualization of the scaffolds with the newly developed cartilage tissue and demonstrate that the scaffolds’ purpose for chondrogenesis was served successfully in all cases and PCL displayed good biocompatibility. Collagenation of scaffolds led to a higher density of cells on the surfaces but also to a limited penetration within, not fully serving the purpose of a 3D culture
