Alginate Core–Shell Capsules for 3D Cultivation of Adipose-Derived Mesenchymal Stem Cells

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Sabrina Nebel
  • Manuel Lux
  • Sonja Kuth
  • Faina Bider
  • Wolf Dietrich
  • Dominik Egger
  • Aldo R. Boccaccini
  • Cornelia Kasper

External Research Organisations

  • University of Natural Resources and Applied Life Sciences (BOKU)
  • Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU Erlangen-Nürnberg)
  • Karl Landsteiner University of Health Sciences
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Details

Original languageEnglish
Article number66
Number of pages15
JournalBioengineering
Volume9
Issue number2
Publication statusPublished - 6 Feb 2022
Externally publishedYes

Abstract

Mesenchymal stem cells (MSCs) are primary candidates in tissue engineering and stem cell therapies due to their intriguing regenerative and immunomodulatory potential. Their ability to self-assemble into three-dimensional (3D) aggregates further improves some of their therapeutic properties, e.g., differentiation potential, secretion of cytokines, and homing capacity after administration. However, high hydrodynamic shear forces and the resulting mechanical stresses within commercially available dynamic cultivation systems can decrease their regenerative properties. Cells embedded within a polymer matrix, however, lack cell-to-cell interactions found in their physiological environment. Here, we present a “semi scaffold-free” approach to protect the cells from high shear forces by a physical barrier, but still allow formation of a 3D structure with in vivo-like cell-to-cell contacts. We highlight a relatively simple method to create core–shell capsules by inverse gelation. The capsules consist of an outer barrier made from sodium alginate, which allows for nutrient and waste diffusion and an inner compartment for direct cell-cell interactions. Next to capsule characterization, a harvesting procedure was established and viability and proliferation of human adipose-derived MSCs were investigated. In the future, this encapsulation and cultivation tech-nique might be used for MSC-expansion in scalable dynamic bioreactor systems, facilitating down-stream procedures, such as cell harvest and differentiation into mature tissue grafts.

Keywords

    3D cell cultivation technologies, Alginate, Cell expansion, Core–shell capsule, Mesenchymal stem cells

ASJC Scopus subject areas

Cite this

Alginate Core–Shell Capsules for 3D Cultivation of Adipose-Derived Mesenchymal Stem Cells. / Nebel, Sabrina; Lux, Manuel; Kuth, Sonja et al.
In: Bioengineering, Vol. 9, No. 2, 66, 06.02.2022.

Research output: Contribution to journalArticleResearchpeer review

Nebel, S, Lux, M, Kuth, S, Bider, F, Dietrich, W, Egger, D, Boccaccini, AR & Kasper, C 2022, 'Alginate Core–Shell Capsules for 3D Cultivation of Adipose-Derived Mesenchymal Stem Cells', Bioengineering, vol. 9, no. 2, 66. https://doi.org/10.3390/bioengineering9020066
Nebel, S., Lux, M., Kuth, S., Bider, F., Dietrich, W., Egger, D., Boccaccini, A. R., & Kasper, C. (2022). Alginate Core–Shell Capsules for 3D Cultivation of Adipose-Derived Mesenchymal Stem Cells. Bioengineering, 9(2), Article 66. https://doi.org/10.3390/bioengineering9020066
Nebel S, Lux M, Kuth S, Bider F, Dietrich W, Egger D et al. Alginate Core–Shell Capsules for 3D Cultivation of Adipose-Derived Mesenchymal Stem Cells. Bioengineering. 2022 Feb 6;9(2):66. doi: 10.3390/bioengineering9020066
Nebel, Sabrina ; Lux, Manuel ; Kuth, Sonja et al. / Alginate Core–Shell Capsules for 3D Cultivation of Adipose-Derived Mesenchymal Stem Cells. In: Bioengineering. 2022 ; Vol. 9, No. 2.
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title = "Alginate Core–Shell Capsules for 3D Cultivation of Adipose-Derived Mesenchymal Stem Cells",
abstract = "Mesenchymal stem cells (MSCs) are primary candidates in tissue engineering and stem cell therapies due to their intriguing regenerative and immunomodulatory potential. Their ability to self-assemble into three-dimensional (3D) aggregates further improves some of their therapeutic properties, e.g., differentiation potential, secretion of cytokines, and homing capacity after administration. However, high hydrodynamic shear forces and the resulting mechanical stresses within commercially available dynamic cultivation systems can decrease their regenerative properties. Cells embedded within a polymer matrix, however, lack cell-to-cell interactions found in their physiological environment. Here, we present a “semi scaffold-free” approach to protect the cells from high shear forces by a physical barrier, but still allow formation of a 3D structure with in vivo-like cell-to-cell contacts. We highlight a relatively simple method to create core–shell capsules by inverse gelation. The capsules consist of an outer barrier made from sodium alginate, which allows for nutrient and waste diffusion and an inner compartment for direct cell-cell interactions. Next to capsule characterization, a harvesting procedure was established and viability and proliferation of human adipose-derived MSCs were investigated. In the future, this encapsulation and cultivation tech-nique might be used for MSC-expansion in scalable dynamic bioreactor systems, facilitating down-stream procedures, such as cell harvest and differentiation into mature tissue grafts.",
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note = "Funding Information: Parts of this project were funded by the Doctoral School BioMatInt. Acknowledgments: We thank Markus Hofinger, Thomas Dalik, the Department of Food Science and Technology, and the Department of Chemistry for providing thickening agents for the initial testing; Christian Obruca (University Hospital Tulln) for enabling collection of human tissue; as well as Erik Reimhult and Eva-Kathrin Ehmoser from the Department of Nanobiotechnology for their advice and expertise. Further, we thank Monika Debreczeny for her help with the microscope ex-periments. The CLSM was kindly provided by the BOKU Core Facilities Multiscale Imaging. Funding Information: Funding: Parts of this project were funded by the Doctoral School BioMatInt. ",
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T1 - Alginate Core–Shell Capsules for 3D Cultivation of Adipose-Derived Mesenchymal Stem Cells

AU - Nebel, Sabrina

AU - Lux, Manuel

AU - Kuth, Sonja

AU - Bider, Faina

AU - Dietrich, Wolf

AU - Egger, Dominik

AU - Boccaccini, Aldo R.

AU - Kasper, Cornelia

N1 - Funding Information: Parts of this project were funded by the Doctoral School BioMatInt. Acknowledgments: We thank Markus Hofinger, Thomas Dalik, the Department of Food Science and Technology, and the Department of Chemistry for providing thickening agents for the initial testing; Christian Obruca (University Hospital Tulln) for enabling collection of human tissue; as well as Erik Reimhult and Eva-Kathrin Ehmoser from the Department of Nanobiotechnology for their advice and expertise. Further, we thank Monika Debreczeny for her help with the microscope ex-periments. The CLSM was kindly provided by the BOKU Core Facilities Multiscale Imaging. Funding Information: Funding: Parts of this project were funded by the Doctoral School BioMatInt.

PY - 2022/2/6

Y1 - 2022/2/6

N2 - Mesenchymal stem cells (MSCs) are primary candidates in tissue engineering and stem cell therapies due to their intriguing regenerative and immunomodulatory potential. Their ability to self-assemble into three-dimensional (3D) aggregates further improves some of their therapeutic properties, e.g., differentiation potential, secretion of cytokines, and homing capacity after administration. However, high hydrodynamic shear forces and the resulting mechanical stresses within commercially available dynamic cultivation systems can decrease their regenerative properties. Cells embedded within a polymer matrix, however, lack cell-to-cell interactions found in their physiological environment. Here, we present a “semi scaffold-free” approach to protect the cells from high shear forces by a physical barrier, but still allow formation of a 3D structure with in vivo-like cell-to-cell contacts. We highlight a relatively simple method to create core–shell capsules by inverse gelation. The capsules consist of an outer barrier made from sodium alginate, which allows for nutrient and waste diffusion and an inner compartment for direct cell-cell interactions. Next to capsule characterization, a harvesting procedure was established and viability and proliferation of human adipose-derived MSCs were investigated. In the future, this encapsulation and cultivation tech-nique might be used for MSC-expansion in scalable dynamic bioreactor systems, facilitating down-stream procedures, such as cell harvest and differentiation into mature tissue grafts.

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KW - 3D cell cultivation technologies

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KW - Cell expansion

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