Effect of electrical stimulation on chondrogenic differentiation of mesenchymal stem cells cultured in hyaluronic acid – Gelatin injectable hydrogels

•The mathematical model allowed to design a bioreactor that stimulates 3D cultures.•Round cell morphologies were acquired and preserved after electric stimulation.•Electrical fields stimulated the expression of SOX-9 and aggrecan.•Glycosaminoglycans expression was higher at the first days of electri...

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Veröffentlicht in:Bioelectrochemistry (Amsterdam, Netherlands) Netherlands), 2020-08, Vol.134, p.107536-107536, Article 107536
Hauptverfasser: Vaca-González, Juan Jairo, Clara-Trujillo, Sandra, Guillot-Ferriols, María, Ródenas-Rochina, Joaquín, Sanchis, María J., Ribelles, José Luis Gómez, Garzón-Alvarado, Diego Alexander, Ferrer, Gloria Gallego
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container_title Bioelectrochemistry (Amsterdam, Netherlands)
container_volume 134
creator Vaca-González, Juan Jairo
Clara-Trujillo, Sandra
Guillot-Ferriols, María
Ródenas-Rochina, Joaquín
Sanchis, María J.
Ribelles, José Luis Gómez
Garzón-Alvarado, Diego Alexander
Ferrer, Gloria Gallego
description •The mathematical model allowed to design a bioreactor that stimulates 3D cultures.•Round cell morphologies were acquired and preserved after electric stimulation.•Electrical fields stimulated the expression of SOX-9 and aggrecan.•Glycosaminoglycans expression was higher at the first days of electric stimulation.•Collagen type II normalized to total collagen increased in stimulated hydrogels. Electrical stimulation (ES) has provided enhanced chondrogenesis of mesenchymal stem cells (MSCs) cultured in micro-mass without the addition of exogenous growth factors. In this study, we demonstrate for the first time that ES of MSCs encapsulated in an injectable hyaluronic acid (HA) – gelatin (GEL) mixture enhances the chondrogenic potential of the hydrogel. Samples were stimulated for 21 days with 10 mV/cm at 60 kHz, applied for 30 min every 6 h a day. Mechanical properties of hydrogels were higher if the precursors were dissolved in Calcium-Free Krebs Ringer Buffer (G′ = 1141 ± 23 Pa) compared to those diluted in culture media (G′ = 213 ± 19 Pa). Cells within stimulated hydrogels were rounder (55%) than non-stimulated cultures (32%) (p = 0.005). Chondrogenic markers such as SOX-9 and aggrecan were higher in stimulated hydrogels compared to controls. The ES demonstrated that normalized content of glycosaminoglycans and collagen to DNA was slightly higher in stimulated samples. Additionally, collagen type II normalized to total collagen was 2.43 times higher in stimulated hydrogels. These findings make ES a promising tool for enhancing articular cartilage tissue engineering outcomes by combining hydrogels and MSCs.
doi_str_mv 10.1016/j.bioelechem.2020.107536
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Electrical stimulation (ES) has provided enhanced chondrogenesis of mesenchymal stem cells (MSCs) cultured in micro-mass without the addition of exogenous growth factors. In this study, we demonstrate for the first time that ES of MSCs encapsulated in an injectable hyaluronic acid (HA) – gelatin (GEL) mixture enhances the chondrogenic potential of the hydrogel. Samples were stimulated for 21 days with 10 mV/cm at 60 kHz, applied for 30 min every 6 h a day. Mechanical properties of hydrogels were higher if the precursors were dissolved in Calcium-Free Krebs Ringer Buffer (G′ = 1141 ± 23 Pa) compared to those diluted in culture media (G′ = 213 ± 19 Pa). Cells within stimulated hydrogels were rounder (55%) than non-stimulated cultures (32%) (p = 0.005). Chondrogenic markers such as SOX-9 and aggrecan were higher in stimulated hydrogels compared to controls. The ES demonstrated that normalized content of glycosaminoglycans and collagen to DNA was slightly higher in stimulated samples. 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Electrical stimulation (ES) has provided enhanced chondrogenesis of mesenchymal stem cells (MSCs) cultured in micro-mass without the addition of exogenous growth factors. In this study, we demonstrate for the first time that ES of MSCs encapsulated in an injectable hyaluronic acid (HA) – gelatin (GEL) mixture enhances the chondrogenic potential of the hydrogel. Samples were stimulated for 21 days with 10 mV/cm at 60 kHz, applied for 30 min every 6 h a day. Mechanical properties of hydrogels were higher if the precursors were dissolved in Calcium-Free Krebs Ringer Buffer (G′ = 1141 ± 23 Pa) compared to those diluted in culture media (G′ = 213 ± 19 Pa). Cells within stimulated hydrogels were rounder (55%) than non-stimulated cultures (32%) (p = 0.005). Chondrogenic markers such as SOX-9 and aggrecan were higher in stimulated hydrogels compared to controls. The ES demonstrated that normalized content of glycosaminoglycans and collagen to DNA was slightly higher in stimulated samples. Additionally, collagen type II normalized to total collagen was 2.43 times higher in stimulated hydrogels. These findings make ES a promising tool for enhancing articular cartilage tissue engineering outcomes by combining hydrogels and MSCs.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>32335352</pmid><doi>10.1016/j.bioelechem.2020.107536</doi><tpages>1</tpages></addata></record>
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subjects Aggrecan
Animals
Calcium
Calcium buffering
Cartilage
Cartilage (articular)
Cell culture
Cell Culture Techniques
Cell differentiation
Cell Differentiation - drug effects
Cell Proliferation - drug effects
Cell Survival - drug effects
Chondrogenesis
Chondrogenesis - drug effects
Chondrogenic differentiation
Collagen
Collagen (type II)
Culture media
Deoxyribonucleic acid
DNA
Electric fields
Electric Stimulation
Electrical stimuli
Gelatin
Gelatin - chemistry
Gelatin, Mesenchymal stem cells
Glycosaminoglycans
Growth factors
Hyaluronic acid
Hyaluronic Acid - chemistry
Hyaluronic Acid - pharmacology
Hydrogels
Hydrogels - chemistry
Hydroxyapatite
Injectable hydrogels
Injections
Mechanical properties
Mesenchymal stem cells
Mesenchymal Stem Cells - cytology
Mesenchymal Stem Cells - drug effects
Stem cells
Stimulation
Swine
Time Factors
Tissue engineering
title Effect of electrical stimulation on chondrogenic differentiation of mesenchymal stem cells cultured in hyaluronic acid – Gelatin injectable hydrogels
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