Electrical stimulation of adipose-derived mesenchymal stem cells in conductive scaffolds and the roles of voltage-gated ion channels

[Display omitted] Since electrical stimulation (ES) can significantly accelerate bone healing, a conductive scaffold that can deliver ES locally at the defect site is desirable for bone defect therapy. Herein, an electrically conductive scaffold was prepared via incorporation of polypyrrole (PPY) in...

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Veröffentlicht in:Acta biomaterialia 2016-03, Vol.32, p.46-56
Hauptverfasser: Zhang, Jieyu, Li, Min, Kang, En-Tang, Neoh, Koon Gee
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Neoh, Koon Gee
description [Display omitted] Since electrical stimulation (ES) can significantly accelerate bone healing, a conductive scaffold that can deliver ES locally at the defect site is desirable for bone defect therapy. Herein, an electrically conductive scaffold was prepared via incorporation of polypyrrole (PPY) in a polycaprolactone (PCL) template scaffold. In vitro tests with mouse osteoblasts indicate that the PPY/PCL scaffold has good biocompatibility, and is suitable for use as an ES substrate. When human adipose-derived mesenchymal stem cells (AD-MSCs) were cultured in the PPY/PCL scaffold and subjected to 200μA of direct current for 4h per day for 21days, the amount of calcium deposited was 100% higher than that without ES. When these cells were subjected to ES together with blockers of voltage-gated calcium (Ca2+v), sodium (Na+v), potassium (K+v), or chloride (Cl−v) channels, the ES-induced enhancement of AD-MSCs’ functions was reduced with Na+v, K+v, or Cl−v blockers and completely nullified with Ca2+v blocker. These results indicate that ion fluxes through these channels activated by ES induce different cascades of reactions in the cells, which subsequently regulate AD-MSCs’ functions, and Ca2+v plays a more critical role than the other three channels. Our results further the current understanding of the mechanisms by which ES regulates stem cells’ behavior, and also showed that the conductive PPY/PCL scaffold with application of ES has good potential in bone defect therapy. In this work, an electrically conductive and biocompatible scaffold was prepared by incorporating polypyrrole in a polycaprolactone template scaffold. Application of 200μA direct current for 4h per day to human adipose derived-mesenchymal stem cells cultured on this scaffold promoted migration of these cells into the inner region of the scaffold and enhanced their osteogenic differentiation. The roles of voltage-gated ion channels (Ca2+v, Na+v, K+v and Cl−v) in osteogenic differentiation stimulated by the electric current were investigated. The results from these experiments further the current understanding of the mechanisms by which electrical stimulation regulates stem cells’ behavior, and also show that the polypyrrole–polycaprolactone scaffold with application of electrical stimulation has good potential in bone defect therapy.
doi_str_mv 10.1016/j.actbio.2015.12.024
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Herein, an electrically conductive scaffold was prepared via incorporation of polypyrrole (PPY) in a polycaprolactone (PCL) template scaffold. In vitro tests with mouse osteoblasts indicate that the PPY/PCL scaffold has good biocompatibility, and is suitable for use as an ES substrate. When human adipose-derived mesenchymal stem cells (AD-MSCs) were cultured in the PPY/PCL scaffold and subjected to 200μA of direct current for 4h per day for 21days, the amount of calcium deposited was 100% higher than that without ES. When these cells were subjected to ES together with blockers of voltage-gated calcium (Ca2+v), sodium (Na+v), potassium (K+v), or chloride (Cl−v) channels, the ES-induced enhancement of AD-MSCs’ functions was reduced with Na+v, K+v, or Cl−v blockers and completely nullified with Ca2+v blocker. These results indicate that ion fluxes through these channels activated by ES induce different cascades of reactions in the cells, which subsequently regulate AD-MSCs’ functions, and Ca2+v plays a more critical role than the other three channels. Our results further the current understanding of the mechanisms by which ES regulates stem cells’ behavior, and also showed that the conductive PPY/PCL scaffold with application of ES has good potential in bone defect therapy. In this work, an electrically conductive and biocompatible scaffold was prepared by incorporating polypyrrole in a polycaprolactone template scaffold. Application of 200μA direct current for 4h per day to human adipose derived-mesenchymal stem cells cultured on this scaffold promoted migration of these cells into the inner region of the scaffold and enhanced their osteogenic differentiation. The roles of voltage-gated ion channels (Ca2+v, Na+v, K+v and Cl−v) in osteogenic differentiation stimulated by the electric current were investigated. 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Herein, an electrically conductive scaffold was prepared via incorporation of polypyrrole (PPY) in a polycaprolactone (PCL) template scaffold. In vitro tests with mouse osteoblasts indicate that the PPY/PCL scaffold has good biocompatibility, and is suitable for use as an ES substrate. When human adipose-derived mesenchymal stem cells (AD-MSCs) were cultured in the PPY/PCL scaffold and subjected to 200μA of direct current for 4h per day for 21days, the amount of calcium deposited was 100% higher than that without ES. When these cells were subjected to ES together with blockers of voltage-gated calcium (Ca2+v), sodium (Na+v), potassium (K+v), or chloride (Cl−v) channels, the ES-induced enhancement of AD-MSCs’ functions was reduced with Na+v, K+v, or Cl−v blockers and completely nullified with Ca2+v blocker. These results indicate that ion fluxes through these channels activated by ES induce different cascades of reactions in the cells, which subsequently regulate AD-MSCs’ functions, and Ca2+v plays a more critical role than the other three channels. Our results further the current understanding of the mechanisms by which ES regulates stem cells’ behavior, and also showed that the conductive PPY/PCL scaffold with application of ES has good potential in bone defect therapy. In this work, an electrically conductive and biocompatible scaffold was prepared by incorporating polypyrrole in a polycaprolactone template scaffold. Application of 200μA direct current for 4h per day to human adipose derived-mesenchymal stem cells cultured on this scaffold promoted migration of these cells into the inner region of the scaffold and enhanced their osteogenic differentiation. The roles of voltage-gated ion channels (Ca2+v, Na+v, K+v and Cl−v) in osteogenic differentiation stimulated by the electric current were investigated. The results from these experiments further the current understanding of the mechanisms by which electrical stimulation regulates stem cells’ behavior, and also show that the polypyrrole–polycaprolactone scaffold with application of electrical stimulation has good potential in bone defect therapy.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>26703122</pmid><doi>10.1016/j.actbio.2015.12.024</doi><tpages>11</tpages></addata></record>
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subjects Adipose Tissue - cytology
Adipose-derived mesenchymal stem cells
Animals
Biocompatibility
Biocompatible Materials - pharmacology
Bones
Cell Differentiation - drug effects
Cell Line
Cell Proliferation - drug effects
Cells, Cultured
Channels
Defects
Electric Stimulation
Electrical stimulation
Electrically conductive
Humans
Ion Channels - metabolism
Membrane Transport Modulators - pharmacology
Mesenchymal Stem Cells - cytology
Mesenchymal Stem Cells - drug effects
Mice
Microscopy, Electron, Scanning
Osteoblasts - cytology
Osteoblasts - drug effects
Osteogenesis - drug effects
Photoelectron Spectroscopy
Polycaprolactone scaffold
Polyesters - pharmacology
Polymers - pharmacology
Polypyrrole
Pyrroles - pharmacology
Scaffolds
Stem cells
Stimulation
Tissue Scaffolds - chemistry
Voltage-gated ion channels
title Electrical stimulation of adipose-derived mesenchymal stem cells in conductive scaffolds and the roles of voltage-gated ion channels
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