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Using a Supramolecular Approach to Engineer Modular Hydrogel Platforms for Culturing Protoplasts – from General Tissue Engineering to Cellular Agriculture

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Abstract

Protoplast regeneration into plant cells and further into plants is an ongoing challenge in agricultural biotechnology. Inspired by mammalian tissue engineering, a strategic shift is proposed in plant tissue engineering to steer protoplast culture using fully synthetic materials-based culture platforms. Here a supramolecular materials method to engineer modular culture methods for protoplasts is chosen to use. Supramolecular monomers as modular building blocks allow to make various hydrogel formulations and to study different protoplast cultures; including 2D cultures on top of supramolecular hydrogels, 2.5D cultures using supramolecular fibers in solution, and 3D cultures when encapsulated in bulk hydrogels or microgels. Importantly, the need is shown for bioactive functionalization of the supramolecular hydrogels with a peptide additive in 2D protoplast cultures. After 11 days, the bioactive hydrogel induced protoplast enlargement, which is absent on pristine hydrogels. The opposite effect is present for protoplasts cultured in 3D, showing plasmolysis as a result of the bioactive additive. Interestingly, in 2.5D lower bioactive additive concentrations in supramolecular fibers stimulated protoplast enlargement, demonstrated by similar morphological changes as in 2D. Finally, protoplast encapsulation in supramolecular microgels is showcased. This work demonstrates the potential to modularly engineer various synthetic platforms to facilitate cellular agriculture.

Original languageEnglish
Article numbere00690
Number of pages13
JournalAdvanced Biology
Volume9
Issue number11
Early online date4 Jun 2025
DOIs
Publication statusPublished - Nov 2025

Bibliographical note

Publisher Copyright:
© 2025 The Author(s). Advanced Biology published by Wiley-VCH GmbH.

Funding

The authors thank Dr. Bart Tiemeijer for introducing us to the microfluidic setup and Dr. Martin Rutten for measuring the rheology measurements (both Eindhoven University of Technology). Nicotiana tabacum L. cv. Bright Yellow 2 (tobacco BY-2) cells genetically modified with the fluorescent protein DsRed were kindly obtained via Prof. Dr. Stefan Schillberg (Fraunhofer Institute for Molecular Biology and Applied Ecology IME). This work was financially supported by a VICI grant from the Netherlands Organization for Scientific Research (NWO, VI.C.222.088), the Ministry of Education, Culture and Science (Gravity Program 024.005.020), and the European Union's Horizon research and innovation program under grant agreement 101079482 (‘SUPRALIFE’). Figures were made with BioRender software. The authors thank Dr. Bart Tiemeijer for introducing us to the microfluidic setup and Dr. Martin Rutten for measuring the rheology measurements (both Eindhoven University of Technology). L. cv. Bright Yellow 2 (tobacco BY‐2) cells genetically modified with the fluorescent protein DsRed were kindly obtained via Prof. Dr. Stefan Schillberg (Fraunhofer Institute for Molecular Biology and Applied Ecology IME). This work was financially supported by a VICI grant from the Netherlands Organization for Scientific Research (NWO, VI.C.222.088), the Ministry of Education, Culture and Science (Gravity Program 024.005.020), and the European Union's Horizon research and innovation program under grant agreement 101079482 (‘SUPRALIFE’). Figures were made with BioRender software. Nicotiana tabacum

Keywords

  • cell wall regeneration
  • cellular agriculture
  • protoplast regeneration
  • supramolecular hydrogels
  • tobacco BY-2
  • Tissue Engineering/methods
  • Cell Culture Techniques/methods
  • Protoplasts/cytology
  • Hydrogels/chemistry

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