AI Article Synopsis

  • Gelatin methacryloyl (GelMA) has been adapted to create a bio-ink from fish skin for 3D bioprinting, providing a more sustainable alternative to traditional mammalian sources.
  • The study involved assessing the physical-mechanical properties of various GelMA concentrations and incorporating human adipose-derived stem cells (ASCs) and platelet lysate into the bio-ink for enhanced functionality.
  • In vivo tests on rat models showed that the ASCs + HPL-loaded GelMA scaffolds promoted better wound healing by improving cell viability, collagen deposition, and blood vessel formation compared to untreated conditions.

Article Abstract

Gelatin methacryloyl (GelMA), typically derived from mammalian sources, has recently emerged as an ideal bio-ink for three-dimensional (3D) bioprinting. Herein, we developed a fish skin-based GelMA bio-ink for the fabrication of a 3D GelMA skin substitute with a 3D bioprinter. Several concentrations of methacrylic acid anhydride were used to fabricate GelMA, in which their physical-mechanical properties were assessed. This fish skin-based GelMA bio-ink was loaded with human adipose tissue-derived mesenchymal stromal cells (ASCs) and human platelet lysate (HPL) and then printed to obtain 3D ASCs + HPL-loaded GelMA scaffolds. Cell viability test and a preliminary investigation of its effectiveness in promoting wound closure were evaluated in a critical-sized full thickness skin defect in a rat model. The cell viability results showed that the number of ASCs increased significantly within the 3D GelMA hydrogel scaffold, indicating its biocompatibility property. In vivo results demonstrated that ASCs + HPL-loaded GelMA scaffolds could delay wound contraction, markedly enhanced collagen deposition, and promoted the formation of new blood vessels, especially at the wound edge, compared to the untreated group. Therefore, this newly fish skin-based GelMA bio-ink developed in this study has the potential to be utilized for the printing of 3D GelMA skin substitutes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11455937PMC
http://dx.doi.org/10.1038/s41598-024-73774-1DOI Listing

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