Peripheral blood aspirates overexpressing IGF-I via rAAV gene transfer undergo enhanced chondrogenic differentiation processes.
Janina FrischPatrick OrthAna Rey-RicoJagadeesh Kumar VenkatesanGertrud SchmittHenning MadryDieter KohnMagali CucchiariniPublished in: Journal of cellular and molecular medicine (2017)
Implantation of peripheral blood aspirates induced towards chondrogenic differentiation upon genetic modification in sites of articular cartilage injury may represent a powerful strategy to enhance cartilage repair. Such a single-step approach may be less invasive than procedures based on the use of isolated or concentrated MSCs, simplifying translational protocols in patients. In this study, we provide evidence showing the feasibility of overexpressing the mitogenic and pro-anabolic insulin-like growth factor I (IGF-I) in human peripheral blood aspirates via rAAV-mediated gene transfer, leading to enhanced proliferative and chondrogenic differentiation (proteoglycans, type-II collagen, SOX9) activities in the samples relative to control (reporter rAAV-lacZ) treatment over extended periods of time (at least 21 days, the longest time-point evaluated). Interestingly, IGF-I gene transfer also triggered hypertrophic, osteo- and adipogenic differentiation processes in the aspirates, suggesting that careful regulation of IGF-I expression may be necessary to contain these events in vivo. Still, the current results demonstrate the potential of targeting human peripheral blood aspirates via therapeutic rAAV transduction as a novel, convenient tool to treat articular cartilage injuries.
Keyphrases
- peripheral blood
- mesenchymal stem cells
- genome wide
- endothelial cells
- binding protein
- copy number
- growth hormone
- pi k akt
- end stage renal disease
- high glucose
- induced pluripotent stem cells
- stem cells
- newly diagnosed
- ejection fraction
- chronic kidney disease
- genome wide identification
- pluripotent stem cells
- bone marrow
- crispr cas
- prognostic factors
- gene expression
- cell proliferation
- signaling pathway
- diabetic rats
- oxidative stress
- wound healing
- long non coding rna