Initial In Vitro Development of a Potassium-Based Intra-Articular Injection for Osteoarthritis

The long-term goal of this work is to develop a potassium (K + )-based intra-articular (IA) injection for osteoarthritis treatment. Within this context, the objectives of this study were to (1) demonstrate that hyperosmolar K + solutions can suppress proinflammatory macrophage activation and (2) eva...

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Veröffentlicht in:Tissue engineering. Part A 2018-09, Vol.24 (17-18), p.139-1392
Hauptverfasser: Erndt-Marino, Josh, Diaz-Rodriguez, Patricia, Hahn, Mariah S.
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Sprache:eng
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Zusammenfassung:The long-term goal of this work is to develop a potassium (K + )-based intra-articular (IA) injection for osteoarthritis treatment. Within this context, the objectives of this study were to (1) demonstrate that hyperosmolar K + solutions can suppress proinflammatory macrophage activation and (2) evaluate the therapeutic potential of a hyperosmolar K + solution relative to a clinically utilized drug-based (methylprednisolone acetate [MPA]—a corticosteroid) or cell-based (human mesenchymal stem cell [hMSC]) IA injectable. A 3D in vitro model with poly(ethylene glycol) diacrylate hydrogels encapsulated with proinflammatory interferon-gamma (IFN)-stimulated macrophages (M(IFN)s) was utilized. Long-term changes in cell phenotype in response to short-term stimulation (i.e., mimicking an IA injection) were assessed following treatment with 80 mM K + gluconate, hMSCs, or MPA. Addition of 80 mM K + gluconate to culture media significantly reduced iNOS and TNF protein levels in M(IFN)s. Furthermore, short-term stimulation with K + gluconate elicited a significant increase in the anti/proinflammatory cytokine profile in M(IFN)s, a response that is not noticed with either clinically utilized MPA or an hMSC injectable. Hyperosmolar K + solutions are capable of attenuating proinflammatory macrophage activation. Moreover, when evaluated in an in vitro setting mimicking an IA injection, K + performed significantly better than hMSCs or the corticosteroid MPA. Cumulatively, these results support further development and application of a K + -based IA injection toward osteoarthritis research.
ISSN:1937-3341
1937-335X
DOI:10.1089/ten.tea.2017.0390