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Electrospun Fibrous Scaffolds of Poly(glycerol-dodecanedioate) for Engineering Neural Tissues From Mouse Embryonic Stem Cells
Published on: June 18, 2014
Functionalized poly(γ-Glutamic Acid) fibrous scaffolds for tissue engineering.
Cristina Gentilini1, Yixiang Dong, Jessica R May
1Department of Materials and Department of Bioengineering, Imperial College London, London SW7 2AZ, UK.
Advanced Healthcare Materials
|November 28, 2012
Summary
New poly(γ-glutamic acid) scaffolds show enhanced cell adhesion and osteogenic differentiation for tissue engineering. Benzyl modification significantly improves cell interactions compared to other esters and PLLA, highlighting its role in biomaterial design.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Polymer Chemistry
Background:
- Poly(γ-glutamic acid) (γ-PGA) is a biocompatible, natural polymer with superior hydrolysis resistance compared to polyesters like PLLA.
- γ-PGA offers functionalizable carboxyl groups, making it suitable for scaffold development.
- Existing tissue engineering scaffolds often face limitations in biocompatibility and cell interaction.
Purpose of the Study:
- To engineer water-resistant fibrous scaffolds from esterified γ-PGA.
- To evaluate the cell adhesion, viability, and osteogenic differentiation potential of these scaffolds.
- To investigate the role of benzyl modification in cell-material interactions.
Main Methods:
- Synthesis of ethyl (Et), propyl (Pr), and benzyl (Bn) esterified γ-PGA scaffolds.
- Assessment of scaffold cytotoxicity and cell adhesion using human mesenchymal stem cells (hMSCs).
- Evaluation of hMSC viability, osteogenic differentiation (alkaline phosphatase, Runx2 expression), protein adsorption, and fibronectin conformation.
Main Results:
- All γ-PGA scaffolds were non-cytotoxic.
- γ-PGA-Bn scaffolds demonstrated significantly increased hMSC adhesion and viability compared to γ-PGA-Et, γ-PGA-Pr, and PLLA scaffolds.
- Cell attachment on partially modified γ-PGA-Bn scaffolds was restored by RGD peptide conjugation, confirming peptide accessibility.
- γ-PGA-Bn scaffolds supported hMSC differentiation towards an osteogenic lineage.
Conclusions:
- Esterified γ-PGA scaffolds, particularly γ-PGA-Bn, are versatile and effective for tissue engineering applications.
- Aromatic functionality, specifically benzyl modification, plays a crucial role in enhancing cell-scaffold interactions.
- These findings suggest γ-PGA-Bn as a promising biomaterial for bone tissue regeneration.

