4.7 Article

Scaffolds from Self-Assembling Tetrapeptides Support 3D Spreading, Osteogenic Differentiation, and Angiogenesis of Mesenchymal Stem Cells

Journal

BIOMACROMOLECULES
Volume 22, Issue 5, Pages 2094-2106

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.biomac.1c00205

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Funding

  1. King Abdullah University of Science and Technology

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Using self-assembling tetrapeptide scaffolds can promote the growth and osteogenic differentiation of human mesenchymal stem cells, with the ability to adjust stiffness by changing concentration; the scaffold can also enhance angiogenesis of human umbilical vein endothelial cells in vitro, indicating great potential for bone tissue engineering applications.
The apparent rise of bone disorders demands advanced treatment protocols involving tissue engineering. Here, we describe self-assembling tetrapeptide scaffolds for the growth and osteogenic differentiation of human mesenchymal stem cells (hMSCs). The rationally designed peptides are synthetic amphiphilic self-assembling peptides composed of four amino acids that are nontoxic. These tetrapeptides can quickly solidify to nanofibrous hydrogels that resemble the extracellular matrix and provide a three-dimensional (3D) environment for cells with suitable mechanical properties. Furthermore, we can easily tune the stiffness of these peptide hydrogels by just increasing the peptide concentration, thus providing a wide range of peptide hydrogels with different stiffnesses for 3D cell culture applications. Since successful bone regeneration requires both osteogenesis and vascularization, our scaffold was found to be able to promote angiogenesis of human umbilical vein endothelial cells (HUVECs) in vitro. The results presented suggest that ultrashort peptide hydrogels are promising candidates for applications in bone tissue engineering.

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