Stem cell spheroid engineering with osteoinductive and ROS scavenging nanofibers for bone regeneration.
Ha Yeon ByunGyu Nam JangJinkyu LeeMin-Ho HongHyunjung ShinHeungsoo ShinPublished in: Biofabrication (2020)
Stem cell spheroids have been widely investigated to accelerate bone tissue regeneartion. However, the directed differentiation of stem cells into osteoblastic lineage and the prevention of cells from damage by reactive oxygen species (ROS) remain challenge. Here, we developed osteoinductive and ROS scavenging extracellular matrix (ECM)-mimicking synthetic fibers based on epigallocatechin gallate (EGCG) coating. They were then utilized to fabricate engineered spheroids with human adipose-derived stem cells (hADSCs) for bone tissue regeneation. The EGCG-mineral fibers (EMF) effectively conferred osteoinductive and ROS scavenging signals on the hADSCs within spheroids, demonstrating relative upregulation of antioxidant genes (SOD-1 (25.8±2.1) and GPX-1 (3.3±0.1) and greater level of expression of osteogenic markers, RUNX2 (5.8±0.1) and OPN (5.9±0.1), compared to hADSCs in the spheroids without EMF. The in vitro overexpression of osteogenic genes from hADSCs was achieved from absence of osteogenic supplenments. Furthermore, in vivo transplantation of hADSCs spheroids with the EMF significantly promoted calvarial bone regeneration (48.39±9.24%) compared to that from defect only (17.38±6.63%), suggesting that the stem cell spheroid biofabrication system with our novel mineralization method described here is a promising tool for bone tissue regeneration.
Keyphrases
- bone regeneration
- stem cells
- reactive oxygen species
- extracellular matrix
- mesenchymal stem cells
- dna damage
- cell death
- bone marrow
- cell therapy
- poor prognosis
- oxidative stress
- genome wide
- endothelial cells
- transcription factor
- dna methylation
- bone mineral density
- gene expression
- bioinformatics analysis
- binding protein
- single cell
- body composition
- induced pluripotent stem cells
- genome wide analysis
- soft tissue
- cell fate