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 technique might be used for MSC-expansion in scalable dynamic bioreactor systems, facilitating downstream procedures, such as cell harvest and differentiation into mature tissue grafts.

Highlights

  • Adipose-derived mesenchymal stem cells are primary candidates in tissue engineering and stem cell therapies due to their intriguing regenerative potential, immunomodulatory effects [1,2,3], and availability from different sources [4]

  • Adherent Mesenchymal stem cells (MSCs) were exposed to thickening agent-supplemented medium for 1 or 24 h followed by measuring their metabolic activity

  • After 1 h just slight differences can be seen between the control to the exposed cells, results are significant for the longer exposure, with a significant decrease in signal of PEG6000 and maltodextrin containing samples

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Summary

Introduction

Adipose-derived mesenchymal stem cells (adMSCs) are primary candidates in tissue engineering and stem cell therapies due to their intriguing regenerative potential, immunomodulatory effects [1,2,3], and availability from different sources [4]. The majority of cell-based therapies require large numbers of cells to reach clinical relevance (approximately 1–2 × 106 cells per kilogram of body weight), making large-scale ex-vivo expansion inevitable. Research has transitioning from 2D monolayer cultivation of MSCs on plasticware towards three-dimensional (3D) cultivation, as it provides the cells with a more relevant physiological environment. Their ability to self-assemble into 3D aggregates under dynamic cultures was shown to improve their therapeutic properties, including maintenance of stemness, differentiation potential, secretion of cytokines, and homing capacity after administration [5,6]. Monitoring and recovery are considerably more difficult than in their 2D counterparts [11]

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