Stimulation of Chondrocyte and Bone Marrow Mesenchymal Stem Cell Chondrogenic Response by Polypyrrole and Polypyrrole/Gold Nanoparticles.
Ilona UzielieneAnton PopovViktorija LisyteGabija KugaudaitePaulina BialaglovyteRaminta VaiciuleviciuteGiedrius KvederasEiva BernotieneArunas RamanaviciusPublished in: Polymers (2023)
Bone marrow mesenchymal stem cells (BMMSCs) possess a strong ability to differentiate into the chondrogenic lineage, which is important for cartilage regeneration. External stimuli, such as electrical stimulation (ES), are frequently studied for chondrogenic differentiation of BMMSCs; however, the application of conductive polymers such as polypyrrole (Ppy), has never been used for stimulating BMMSCs chondrogenesis in vitro before. Thus, the aim of this study was to evaluate the chondrogenic potential of human BMMSCs after stimulation with Ppy nanoparticles (Ppy NPs) and compare them to cartilage-derived chondrocytes. In this study, we tested Ppy NPs without and with 13 nm gold NPs (Ppy/Au) for BMMSCs and chondrocyte proliferation, viability, and chondrogenic differentiation for 21 days, without the use of ES. The results demonstrated significantly higher amounts of cartilage oligomeric matrix protein (COMP) in BMMSCs stimulated with Ppy and Ppy/Au NPs, as compared to the control. The expression of chondrogenic genes ( SOX9 , ACAN , COL2A1 ) in BMMSCs and chondrocytes were upregulated by Ppy and Ppy/Au NPs, as compared to controls. Histological staining with safranin-O indicated higher extracellular matrix production in Ppy and Ppy/Au NPs stimulated samples, as compared to controls. In conclusion, Ppy and Ppy/Au NPs stimulate BMMSC chondrogenic differentiation; however, BMMSCs were more responsive to Ppy, while chondrocytes possessed a stronger chondrogenic response to Ppy/Au NPs.
Keyphrases
- mesenchymal stem cells
- extracellular matrix
- reduced graphene oxide
- bone marrow
- gold nanoparticles
- sensitive detection
- stem cells
- risk assessment
- oxide nanoparticles
- transcription factor
- poor prognosis
- gene expression
- quantum dots
- photodynamic therapy
- endothelial cells
- dna methylation
- signaling pathway
- single cell
- tandem mass spectrometry