Selective Formation of Osteogenic and Vasculogenic Tissues for Cartilage Regeneration.
Zeyang LiuHaochen NanYi Shiou ChiouZhen ZhanPeter E LobieChengzhi HuPublished in: Advanced healthcare materials (2022)
Tissue-engineered periosteum substitutes (TEPSs) incorporating hierarchical architecture with osteoprogenitor and vascular niches are drawing much attention as a promising tool to support functional cells in defined zones and nourish the cortical bone. Current TEPSs usually lack technologies to closely observe cell performance, especially at the cell contact interface between distinct compartments containing defined biological configurations and functions. Here, an electrodeposition strategy is reported, which enables the selective formation of TEPSs with osteoprogenitor and vascular niches in a multiphasic scaffold in combination with different human cell types for cartilage regeneration in an in vivo osteochondral defect model. Human umbilical vein endothelial cells (HUVECs), dermal fibroblasts (HDFs), and bone marrow mesenchymal stem cells (hMSCs) are used to mirror both the vascular and osteogenic niches, respectively. It is observed that the intrinsic viscoelastic nature of the porous solid matrix is essential to successfully induce angiogenesis. Coculture of hMSCs with functional cells (HUVECs/HDFs) in TEPSs also effectively promoted periosteal regeneration, including osteogenic and angiogenic processes. The osteoarthritis cartilage histopathology assessment and histologic/histochemical grading system data indicate that the TEPSs containing hMSCs/HUVECs/HDFs exhibit superior potential for cartilage regeneration.
Keyphrases
- endothelial cells
- stem cells
- mesenchymal stem cells
- induced apoptosis
- single cell
- extracellular matrix
- bone marrow
- cell therapy
- wound healing
- cell cycle arrest
- gene expression
- working memory
- vascular endothelial growth factor
- signaling pathway
- risk assessment
- bone mineral density
- high glucose
- cell proliferation
- cell death
- climate change
- pi k akt
- oxidative stress
- electronic health record
- endoplasmic reticulum stress
- artificial intelligence