Samenvatting
Recent advances in the field of ophthalmology show great potential in the design of bioengineered constructs to mimic the corneal stroma. Hydrogels based on synthetic supramolecular polymers, are attractive synthetic mimics of the natural highly hydrated corneal stroma. Here, a fully synthetic corneal stromal construct is developed via engineering of an injectable supramolecular hydrogel based on ureido-pyrimidinone (UPy) moieties. The hydrogel displays a dynamic and tunable behavior, which allows for control of biochemical and mechanical cues. Two hydrogels are developed, a fully synthetic hydrogel functionalized with a bioactive cyclic arginine-glycine-aspartate UPy (UPy-cRGD) additive, and a hybrid hydrogel based on UPy-moieties mixed with collagen type I fibers. Both hydrogels supported cell encapsulation and associated cellular deposition of extracellular matrix (ECM) proteins after 21 days. Excitingly, the hydrogels support the activation of isolated primary keratocytes into stromal fibroblasts as well as the differentiation toward more quiescent corneal stromal keratocytes, demonstrated by their characteristic long dendritic protrusions and a substantially diminished cytokine secretion. Furthermore, cells survive shear stresses during an injectability test. Together, these findings highlight the development of an injectable supramolecular hydrogel as a synthetic corneal stromal microenvironment able to host primary keratocytes.
Originele taal-2 | Engels |
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Artikelnummer | 2301392 |
Aantal pagina's | 14 |
Tijdschrift | Advanced Healthcare Materials |
Volume | 12 |
Nummer van het tijdschrift | 32 |
DOI's | |
Status | Gepubliceerd - 27 dec. 2023 |
Financiering
This research was financially supported by the Ministry of Education, Culture and Science (Gravity Programs 024.001.035 and 024.003.013), and the research program of Chemelot InSciTe, project EyeSciTe. The authors thank the EyeSciTe consortium partners from MERLN Institute for Technology-Inspired Regenerative Medicine and Maastricht UMC+ for providing them with the primary keratocytes. Furthermore, the authors thank Mark C. van Turnhout for his kind help with designing the MatLab script used to create the 3D height indication cell images. Finally, the authors acknowledge Cas van der Putten for the efficient collaboration during general cell culture and optimization of the immunofluorescent stainings.
Financiers | Financiernummer |
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MERLN Institute for Technology-Inspired Regenerative Medicine | |
Ministerie van OCW | 024.003.013, 024.001.035 |
Maastricht University Medical Center |