International Journal of Molecular Sciences · 2020 · 13 citations · 69 references
MedicineBioengineeringOphthalmologyRegenerative MedicineTissue EngineeringWound HealingCorneal PhysiologyCorneal Wound HealingMesenchymal Stem Cell TherapyMesenchymal Stromal Cell TherapyWound Healing PhysiologyWound Healing ResponseCell Viability AssaysCell Viability PreservationCorneal Healing ResponseCorneal Stromal Cell BiologyHypothermic PreservationImmune Cell Infiltration DensitySoluble Protein SecretionWound Healing Gels
Adipose-derived mesenchymal stromal cells (Ad-MSCs) may alleviate corneal injury through the secretion of therapeutic factors delivered at the injury site. We aimed to investigate the therapeutic factors secreted from hypothermically stored, alginate-encapsulated Ad-MSCs’ bandages in in vitro and in vivo corneal wounds. Ad-MSCs were encapsulated in 1.2% w/v alginate gels to form bandages and stored at 15 °C for 72 h before assessing cell viability and co-culture with corneal scratch wounds. Genes of interest, including HGF, TSG-6, and IGF were identified by qPCR and a human cytokine array kit used to profile the therapeutic factors secreted. In vivo, bandages were applied to adult male mice corneas following epithelial debridement. Bandages were shown to maintain Ad-MSCs viability during storage and able to indirectly improve corneal wound healing in vivo. Soluble protein concentration and paracrine factors such as TSG-6, HGF, IL-8, and MCP-1 release were greatest following hypothermic storage. In vivo, Ad-MSCs bandages-treated groups reduced immune cell infiltration when compared to untreated groups. In conclusion, bandages were shown to maintain Ad-MSCs ability to produce a cocktail of key therapeutic factors following storage and that these soluble factors can improve in vitro and in vivo corneal wound healing.
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