Composite Coatings Based on Recombinant Spidroins and Peptides with Motifs of the Extracellular Matrix Proteins Enhance Neuronal Differentiation of Neural Precursor Cells Derived from Human Induced Pluripotent Stem Cells.
Ekaterina V NovosadovaOleg V DolotovLyudmila V NovosadovaLubov I DavydovaKonstantin V SidorukElena L ArsenyevaDarya M ShimchenkoVladimir G DebabovVladimir G BogushVyacheslav Z TarantulPublished in: International journal of molecular sciences (2023)
The production and transplantation of functionally active human neurons is a promising approach to cell therapy. Biocompatible and biodegradable matrices that effectively promote the growth and directed differentiation of neural precursor cells (NPCs) into the desired neuronal types are very important. The aim of this study was to evaluate the suitability of novel composite coatings (CCs) containing recombinant spidroins (RSs) rS1/9 and rS2/12 in combination with recombinant fused proteins (FP) carrying bioactive motifs (BAP) of the extracellular matrix (ECM) proteins for the growth of NPCs derived from human induced pluripotent stem cells (iPSC) and their differentiation into neurons. NPCs were produced by the directed differentiation of human iPSCs. The growth and differentiation of NPCs cultured on different CC variants were compared with a Matrigel (MG) coating using qPCR analysis, immunocytochemical staining, and ELISA. An investigation revealed that the use of CCs consisting of a mixture of two RSs and FPs with different peptide motifs of ECMs increased the efficiency of obtaining neurons differentiated from iPSCs compared to Matrigel. CC consisting of two RSs and FPs with Arg-Gly-Asp-Ser (RGDS) and heparin binding peptide (HBP) is the most effective for the support of NPCs and their neuronal differentiation.
Keyphrases
- induced pluripotent stem cells
- extracellular matrix
- endothelial cells
- cell therapy
- induced apoptosis
- spinal cord
- stem cells
- mesenchymal stem cells
- drug delivery
- dna methylation
- bone marrow
- cell free
- copy number
- growth factor
- signaling pathway
- ionic liquid
- endoplasmic reticulum stress
- spinal cord injury
- dna binding
- tissue engineering
- amino acid
- drug release