4.7 Article

Light Cross-Linkable Marine Collagen for Coaxial Printing of a 3D Model of Neuromuscular Junction Formation

Journal

BIOMEDICINES
Volume 9, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/biomedicines9010016

Keywords

3D bioprinting; neural cell; skeletal muscle cell; neuromuscular junction

Funding

  1. ARC Centre of Excellence for Electromaterials Science [CE140100012]
  2. International Education and Training program
  3. BIOFABrication for future Manufacturing
  4. EU ICI ECP International Joint Program Biofabrication Mobility Grant
  5. ARC Industrial Transformation Training Centre in Additive Biomanufacturing [IC160100026]

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Marine collagen, as an alternative source, shows potential in tissue engineering. The study revealed that marine collagen could serve as a low-cost, customizable, scalable, and quick-to-print platform for drug screening and researching neuromuscular junction physiology and pathogenesis.
Collagen is a major component of the extracellular matrix (ECM) that modulates cell adhesion, growth, and migration, and has been utilised in tissue engineering applications. However, the common terrestrial sources of collagen carry the risk of zoonotic disease transmission and there are religious barriers to the use of bovine and porcine products in many cultures. Marine based collagens offer an attractive alternative and have so far been under-utilized for use as biomaterials for tissue engineering. Marine collagen can be extracted from fish waste products, therefore industry by-products offer an economical and environmentally sustainable source of collagen. In a handful of studies, marine collagen has successfully been methacrylated to form collagen methacrylate (ColMA). Our work included the extraction, characterization and methacrylation of Red Snapper collagen, optimisation of conditions for neural cell seeding and encapsulation using the unmodified collagen, thermally cross-linked, and the methacrylated collagen with UV-induced cross-linking. Finally, the 3D co-axial printing of neural and skeletal muscle cell cultures as a model for neuromuscular junction (NMJ) formation was investigated. Overall, the results of this study show great potential for a novel NMJ in vitro 3D bioprinted model that, with further development, could provide a low-cost, customizable, scalable and quick-to-print platform for drug screening and to study neuromuscular junction physiology and pathogenesis.

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