Incorporation of Human-Platelet-Derived Growth Factor-BB Encapsulated Poly(lactic-co-glycolic acid) Microspheres into 3D CORAGRAF Enhances Osteogenic Differentiation of Mesenchymal Stromal Cells.
Saktiswaren MohanHanumantha Rao Balaji RaghavendranPuvanan KarunanithiMalliga Raman MuraliSangeetha Vasudevaraj NaveenSepehr TalebianMohammad MehraliMehdi MehraliElango NatarajanChee Ken ChanTunku KamarulPublished in: ACS applied materials & interfaces (2017)
Tissue engineering aims to generate or facilitate regrowth or healing of damaged tissues by applying a combination of biomaterials, cells, and bioactive signaling molecules. In this regard, growth factors clearly play important roles in regulating cellular fate. However, uncontrolled release of growth factors has been demonstrated to produce severe side effects on the surrounding tissues. In this study, poly(lactic-co-glycolic acid) (PLGA) microspheres (MS) incorporated three-dimensional (3D) CORAGRAF scaffolds were engineered to achieve controlled release of platelet-derived growth factor-BB (PDGF-BB) for the differentiation of stem cells within the 3D polymer network. Fourier transform infrared spectroscopy, energy-dispersive X-ray spectroscopy, scanning electron microscopy, and microtomography were applied to characterize the fabricated scaffolds. In vitro study revealed that the CORAGRAF-PLGA-PDGF-BB scaffold system enhanced the release of PDGF-BB for the regulation of cell behavior. Stromal cell attachment, viability, release of osteogenic differentiation markers such as osteocalcin, and upregulation of osteogenic gene expression exhibited positive response. Overall, the developed scaffold system was noted to support rapid cell expansion and differentiation of stromal cells into osteogenic cells in vitro for bone tissue engineering applications.
Keyphrases
- growth factor
- tissue engineering
- gene expression
- bone marrow
- electron microscopy
- single cell
- stem cells
- mesenchymal stem cells
- cell therapy
- induced apoptosis
- drug delivery
- high resolution
- cell cycle arrest
- smooth muscle
- multiple sclerosis
- endothelial cells
- dna methylation
- oxidative stress
- cell death
- bone regeneration
- poor prognosis
- bone mineral density
- long non coding rna
- endoplasmic reticulum stress
- molecularly imprinted
- solid phase extraction
- induced pluripotent stem cells
- bone loss