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Methacrylated gellan gum/poly-L-lysine polyelectrolyte complex beads for cell-based therapies

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Bibliographic Details
Summary:Cell encapsulation strategies using hydrogel beads have been considered as an alternative to immunosuppression in cell-based therapies. They rely on layer-by-layer (LbL) deposition of polymers to tune beadsâ permeability, creating a physical barrier to the host immune system. However, the LbL approach can also create diffusion barriers, hampering the flow of essential nutrients and therapeutic cell products. In this work, polyelectrolyte complex (PEC) methodology was used to circumvent the drawbacks of the LbL strategy, by inducing hydrogel beads formation through the interaction of anionic methacrylated gellan gum (GG-MA) with cationic poly-L-lysine (PLL). The interfacial complexation between both polymers resulted in beads with a cell-friendly GG-MA hydrogel core surrounded by a PEC semipermeable membrane. The beads showed great in vitro stability over time, a semi-permeable behavior, and supported human adipose-derived stem cells encapsulation. Additionally, and regarding immune recognition, the in vitro and in vivo studies pointed out that the hydrogel beads behave as an immunocompatible system. Overall, the engineered beads showed great potential for hydrogel-mediated cell therapies, when immunoprotection is required, as when treating different metabolic disorders.
Main Authors:Vieira, Sílvia Cristina Araújo
Other Authors:da Silva Morais, Alain; Garet, E.; Silva-Correia, Joana; Reis, R. L.; Gonzalez-Fernández, A.; Oliveira, Joaquim M.
Subject:Cell therapies Gellan Gum poly-l-lysine Polyelectrolyte Complexes Tissue engineering
Year:2021
Country:Portugal
Document type:article
Access type:restricted access
Associated institution:Universidade do Minho
Language:English
Origin:RepositóriUM - Universidade do Minho
Description
Summary:Cell encapsulation strategies using hydrogel beads have been considered as an alternative to immunosuppression in cell-based therapies. They rely on layer-by-layer (LbL) deposition of polymers to tune beadsâ permeability, creating a physical barrier to the host immune system. However, the LbL approach can also create diffusion barriers, hampering the flow of essential nutrients and therapeutic cell products. In this work, polyelectrolyte complex (PEC) methodology was used to circumvent the drawbacks of the LbL strategy, by inducing hydrogel beads formation through the interaction of anionic methacrylated gellan gum (GG-MA) with cationic poly-L-lysine (PLL). The interfacial complexation between both polymers resulted in beads with a cell-friendly GG-MA hydrogel core surrounded by a PEC semipermeable membrane. The beads showed great in vitro stability over time, a semi-permeable behavior, and supported human adipose-derived stem cells encapsulation. Additionally, and regarding immune recognition, the in vitro and in vivo studies pointed out that the hydrogel beads behave as an immunocompatible system. Overall, the engineered beads showed great potential for hydrogel-mediated cell therapies, when immunoprotection is required, as when treating different metabolic disorders.

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