TY - JOUR
T1 - Chondrogenesis of human adipose-derived mesenchymal stromal cells on the [devitalized costal cartilage matrix/poly(vinyl alcohol)/fibrin] hybrid scaffolds
AU - Setayeshmehr, Mohsen
AU - Esfandiari, Ebrahim
AU - Hashemibeni, Batool
AU - Tavakoli, Amir Hossein
AU - Rafienia, Mohammad
AU - Samadikuchaksaraei, Ali
AU - Moroni, Lorenzo
AU - Joghataei, Mohammad Taghi
N1 - Funding Information:
We would like to thank Dr. Mohammad Kazemi for critical comments on the RT-PCR studies. This work was supported by grants from the Iran University of Medical Sciences , Tehran, Iran.
Publisher Copyright:
© 2019 Elsevier Ltd
PY - 2019/9
Y1 - 2019/9
N2 - Porous scaffolds derived from native cartilage matrix along with autologous cells could be an effective tool for cartilage tissue engineering (CTE). Recently, it was shown that scaffolds based on cartilage extra cellular matrix (ECM) can induce chondrogenesis of human adipose-derived mesenchymal stromal cells (ASCs) without using exogenous growth factors. However, lack of mechanical properties, rapid biodegradation, and contraction of these scaffolds in culture limit further applications. The present study investigated the fabrication of novel scaffolds based on devitalized costal cartilage matrix (DCM) and poly vinyl alcohol (PVA), using genipin as a natural crosslinker. For this purpose, PVA was modified to expose amine groups (PVA-A), which crosslinked with DCM powder via the lowest genipin percentage of 0.04% (wt/wt). The crosslinked scaffolds were characterized by different techniques including porosity percentage, pore size, mechanical properties, crosslinking density, and swelling. ASCs were seeded on the scaffolds using fibrin hydrogel. Gene expression measurements, biochemical assays and histological staining confirmed that ASC-seeded constructs cultured in the chondrogenic medium can express cartilage-specific genes and synthesize cartilage-related macromolecules. In the presence of TGF-beta 3 the constructs exhibited significant expression of these markers compared to the control medium. These findings suggest that [genipin-crosslinked DCM-PVA-A/ fibrin] can be considered as an appealing hybrid scaffold for CTE applications.
AB - Porous scaffolds derived from native cartilage matrix along with autologous cells could be an effective tool for cartilage tissue engineering (CTE). Recently, it was shown that scaffolds based on cartilage extra cellular matrix (ECM) can induce chondrogenesis of human adipose-derived mesenchymal stromal cells (ASCs) without using exogenous growth factors. However, lack of mechanical properties, rapid biodegradation, and contraction of these scaffolds in culture limit further applications. The present study investigated the fabrication of novel scaffolds based on devitalized costal cartilage matrix (DCM) and poly vinyl alcohol (PVA), using genipin as a natural crosslinker. For this purpose, PVA was modified to expose amine groups (PVA-A), which crosslinked with DCM powder via the lowest genipin percentage of 0.04% (wt/wt). The crosslinked scaffolds were characterized by different techniques including porosity percentage, pore size, mechanical properties, crosslinking density, and swelling. ASCs were seeded on the scaffolds using fibrin hydrogel. Gene expression measurements, biochemical assays and histological staining confirmed that ASC-seeded constructs cultured in the chondrogenic medium can express cartilage-specific genes and synthesize cartilage-related macromolecules. In the presence of TGF-beta 3 the constructs exhibited significant expression of these markers compared to the control medium. These findings suggest that [genipin-crosslinked DCM-PVA-A/ fibrin] can be considered as an appealing hybrid scaffold for CTE applications.
KW - Devitalized costal cartilage matrix
KW - Poly vinyl alcohol
KW - Genipin
KW - Hybrid scaffold
KW - Cartilage tissue engineering
KW - TISSUE-ENGINEERED CARTILAGE
KW - COLLAGEN-GAG SCAFFOLDS
KW - ADULT STEM-CELLS
KW - CROSS-LINKING
KW - ARTICULAR-CARTILAGE
KW - IN-VITRO
KW - MECHANICAL-PROPERTIES
KW - BIOLOGICAL TISSUE
KW - MATRIX SYNTHESIS
KW - WOVEN SCAFFOLDS
U2 - 10.1016/j.eurpolymj.2019.04.044
DO - 10.1016/j.eurpolymj.2019.04.044
M3 - Article
SN - 0014-3057
VL - 118
SP - 528
EP - 541
JO - European Polymer Journal
JF - European Polymer Journal
ER -