Effects of photobiomodulation therapy on the extracellular matrix of human dental pulp cell sheets

Photobiomodulation therapy (PBMT) and the cell sheet (CS) technology improve processes relevant to tissue regeneration. The aim of this study was to investigate the effects of different PBMT parameters on the architecture (histology), protein composition (Western blotting and immunohistochemistry) a...

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Veröffentlicht in:Journal of photochemistry and photobiology. B, Biology Biology, 2019-05, Vol.194, p.149-157
Hauptverfasser: Garrido, P.R., Pedroni, A.C.F., Cury, D.P., Moreira, M.S., Rosin, F., Sarra, G., Marques, M.M.
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container_title Journal of photochemistry and photobiology. B, Biology
container_volume 194
creator Garrido, P.R.
Pedroni, A.C.F.
Cury, D.P.
Moreira, M.S.
Rosin, F.
Sarra, G.
Marques, M.M.
description Photobiomodulation therapy (PBMT) and the cell sheet (CS) technology improve processes relevant to tissue regeneration. The aim of this study was to investigate the effects of different PBMT parameters on the architecture (histology), protein composition (Western blotting and immunohistochemistry) and ultrastructure [scanning electron microscopy (SEM) and transmission electron microscopy (TEM)] of the extracellular matrix (ECM) synthesized by CSs composed by human dental pulp stem cells (hDPSCs). Thawed cells were recharacterized by the expression profile of the surface molecules of mesenchymal stem cells (MSCs) using flow cytometry. Clonogenic medium supplemented with vitamin C (20 μg/ml) was used for obtaining the CSs. PBMT was performed with continuous-wave diode laser (660 nm, 20 mW, 0.028cm2, 0.71 W/cm2) in punctual and contact mode. The CSs were allocated in 3 experimental groups: Control: no further treatment; PBMT1 [4 s, 3 J/cm2 (lower energy density), 0.08 J/point] and PBMT2 [7 s, 5 J/cm2 (higher energy density), 0.14 J/point]. Statistical comparisons were performed (p ≤ .05). The cells presented the classical immunoprofile of MSCs. Type I and type III collagens and fibronectin were present in the ECM of the CSs. PBMT1 induced higher amount of fibronectin. The overall ultrastructure of the CSs in the PBMT1 was epithelial-like, whereas the PBMT2 leads to CSs with fusiform cells arranged in bundles. TEM identified a more mature ECM and signs of apoptosis and necrosis in the PBMT2 group. PBMT influence the composition and ultrastructure of the ECM of CSs of hDPSCs. Thus, PBMT, specifically when applied in the lower energy density, could be of importance in the determination of the mechanical quality of CSs, which may favor cell therapy by improving the CS transplantation approach. [Display omitted] •Photobiomodulation therapy (PBMT) is able to improve the characteristics of the cell sheet (CS).•PBMT improved extracellular matrix maturation in CSs, which could facilitate the procedures of cell transplantation.•Fibronectin synthesis was increased by PBMT.•Fibronectin possibly influenced the epithelial-like differentiation of the human dental pulp stem cells (hDPSCs) in the CSs.•PBMT applied with the parameter of 5 J/cm2 induced damage to the hDPSCs in the CSs.
doi_str_mv 10.1016/j.jphotobiol.2019.03.017
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The aim of this study was to investigate the effects of different PBMT parameters on the architecture (histology), protein composition (Western blotting and immunohistochemistry) and ultrastructure [scanning electron microscopy (SEM) and transmission electron microscopy (TEM)] of the extracellular matrix (ECM) synthesized by CSs composed by human dental pulp stem cells (hDPSCs). Thawed cells were recharacterized by the expression profile of the surface molecules of mesenchymal stem cells (MSCs) using flow cytometry. Clonogenic medium supplemented with vitamin C (20 μg/ml) was used for obtaining the CSs. PBMT was performed with continuous-wave diode laser (660 nm, 20 mW, 0.028cm2, 0.71 W/cm2) in punctual and contact mode. The CSs were allocated in 3 experimental groups: Control: no further treatment; PBMT1 [4 s, 3 J/cm2 (lower energy density), 0.08 J/point] and PBMT2 [7 s, 5 J/cm2 (higher energy density), 0.14 J/point]. Statistical comparisons were performed (p ≤ .05). The cells presented the classical immunoprofile of MSCs. Type I and type III collagens and fibronectin were present in the ECM of the CSs. PBMT1 induced higher amount of fibronectin. The overall ultrastructure of the CSs in the PBMT1 was epithelial-like, whereas the PBMT2 leads to CSs with fusiform cells arranged in bundles. TEM identified a more mature ECM and signs of apoptosis and necrosis in the PBMT2 group. PBMT influence the composition and ultrastructure of the ECM of CSs of hDPSCs. Thus, PBMT, specifically when applied in the lower energy density, could be of importance in the determination of the mechanical quality of CSs, which may favor cell therapy by improving the CS transplantation approach. [Display omitted] •Photobiomodulation therapy (PBMT) is able to improve the characteristics of the cell sheet (CS).•PBMT improved extracellular matrix maturation in CSs, which could facilitate the procedures of cell transplantation.•Fibronectin synthesis was increased by PBMT.•Fibronectin possibly influenced the epithelial-like differentiation of the human dental pulp stem cells (hDPSCs) in the CSs.•PBMT applied with the parameter of 5 J/cm2 induced damage to the hDPSCs in the CSs.</description><identifier>ISSN: 1011-1344</identifier><identifier>EISSN: 1873-2682</identifier><identifier>DOI: 10.1016/j.jphotobiol.2019.03.017</identifier><identifier>PMID: 30954874</identifier><language>eng</language><publisher>Switzerland: Elsevier B.V</publisher><subject>Apoptosis ; Ascorbic acid ; Cell sheet ; Collagen ; Collagen (type I) ; Composition ; Continuous radiation ; Density ; Dental materials ; Dental pulp ; Dental pulp stem cells ; Energy ; Extracellular matrix ; Fibronectin ; Flow cytometry ; Flux density ; Histology ; Immunohistochemistry ; Mechanical properties ; Mesenchyme ; Microscopy ; Necrosis ; Photobiomodulation therapy ; Protein composition ; Regeneration ; Scanning electron microscopy ; Scanning transmission electron microscopy ; Semiconductor lasers ; Stem cells ; Therapy ; Tissue engineering ; Transmission electron microscopy ; Transplantation ; Ultrastructure ; Vitamin C ; Western blotting</subject><ispartof>Journal of photochemistry and photobiology. 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B, Biology</title><addtitle>J Photochem Photobiol B</addtitle><description>Photobiomodulation therapy (PBMT) and the cell sheet (CS) technology improve processes relevant to tissue regeneration. The aim of this study was to investigate the effects of different PBMT parameters on the architecture (histology), protein composition (Western blotting and immunohistochemistry) and ultrastructure [scanning electron microscopy (SEM) and transmission electron microscopy (TEM)] of the extracellular matrix (ECM) synthesized by CSs composed by human dental pulp stem cells (hDPSCs). Thawed cells were recharacterized by the expression profile of the surface molecules of mesenchymal stem cells (MSCs) using flow cytometry. Clonogenic medium supplemented with vitamin C (20 μg/ml) was used for obtaining the CSs. PBMT was performed with continuous-wave diode laser (660 nm, 20 mW, 0.028cm2, 0.71 W/cm2) in punctual and contact mode. 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[Display omitted] •Photobiomodulation therapy (PBMT) is able to improve the characteristics of the cell sheet (CS).•PBMT improved extracellular matrix maturation in CSs, which could facilitate the procedures of cell transplantation.•Fibronectin synthesis was increased by PBMT.•Fibronectin possibly influenced the epithelial-like differentiation of the human dental pulp stem cells (hDPSCs) in the CSs.•PBMT applied with the parameter of 5 J/cm2 induced damage to the hDPSCs in the CSs.</description><subject>Apoptosis</subject><subject>Ascorbic acid</subject><subject>Cell sheet</subject><subject>Collagen</subject><subject>Collagen (type I)</subject><subject>Composition</subject><subject>Continuous radiation</subject><subject>Density</subject><subject>Dental materials</subject><subject>Dental pulp</subject><subject>Dental pulp stem cells</subject><subject>Energy</subject><subject>Extracellular matrix</subject><subject>Fibronectin</subject><subject>Flow cytometry</subject><subject>Flux density</subject><subject>Histology</subject><subject>Immunohistochemistry</subject><subject>Mechanical properties</subject><subject>Mesenchyme</subject><subject>Microscopy</subject><subject>Necrosis</subject><subject>Photobiomodulation therapy</subject><subject>Protein composition</subject><subject>Regeneration</subject><subject>Scanning electron microscopy</subject><subject>Scanning transmission electron microscopy</subject><subject>Semiconductor lasers</subject><subject>Stem cells</subject><subject>Therapy</subject><subject>Tissue engineering</subject><subject>Transmission electron microscopy</subject><subject>Transplantation</subject><subject>Ultrastructure</subject><subject>Vitamin C</subject><subject>Western blotting</subject><issn>1011-1344</issn><issn>1873-2682</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkU2L1jAQx4Mo7rr6FSTgxUtr0jQvPeqyvsCCFz2HNJnwpLRNTVLZ_fab8uwqeHEuMzC__8wwf4QwJS0lVHyY2mk7xRLHEOe2I3RoCWsJlc_QJVWSNZ1Q3fNaE0obyvr-Ar3KeSI1uJAv0QUjA--V7C_ReOM92JJx9Php5BLdPpsS4orLCZLZ7vG5xHBXkrEwz7Wf8GJKCneH8rQvZsUO1mJmvO3zhg8I5xNAya_RC2_mDG8e8xX6-fnmx_XX5vb7l2_XH28b2wtVGjM6PvZ25BaENFIIR6RX3gwdF5R1hnbKugG48dJybpQASQQDyq1zxHPDrtD789wtxV875KKXkI87zApxz7rrCO-JYrKv6Lt_0Cnuaa3XVYqxgQlFD0qdKZtizgm83lJYTLrXlOjDBz3pvz7owwdNmK4-VOnbxwX7uID7I3x6fAU-nQGoH_kdIOlsA6wWXEjVD-1i-P-WB_3coFQ</recordid><startdate>20190501</startdate><enddate>20190501</enddate><creator>Garrido, P.R.</creator><creator>Pedroni, A.C.F.</creator><creator>Cury, D.P.</creator><creator>Moreira, M.S.</creator><creator>Rosin, F.</creator><creator>Sarra, G.</creator><creator>Marques, M.M.</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8571-7144</orcidid></search><sort><creationdate>20190501</creationdate><title>Effects of photobiomodulation therapy on the extracellular matrix of human dental pulp cell sheets</title><author>Garrido, P.R. ; 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The aim of this study was to investigate the effects of different PBMT parameters on the architecture (histology), protein composition (Western blotting and immunohistochemistry) and ultrastructure [scanning electron microscopy (SEM) and transmission electron microscopy (TEM)] of the extracellular matrix (ECM) synthesized by CSs composed by human dental pulp stem cells (hDPSCs). Thawed cells were recharacterized by the expression profile of the surface molecules of mesenchymal stem cells (MSCs) using flow cytometry. Clonogenic medium supplemented with vitamin C (20 μg/ml) was used for obtaining the CSs. PBMT was performed with continuous-wave diode laser (660 nm, 20 mW, 0.028cm2, 0.71 W/cm2) in punctual and contact mode. The CSs were allocated in 3 experimental groups: Control: no further treatment; PBMT1 [4 s, 3 J/cm2 (lower energy density), 0.08 J/point] and PBMT2 [7 s, 5 J/cm2 (higher energy density), 0.14 J/point]. Statistical comparisons were performed (p ≤ .05). The cells presented the classical immunoprofile of MSCs. Type I and type III collagens and fibronectin were present in the ECM of the CSs. PBMT1 induced higher amount of fibronectin. The overall ultrastructure of the CSs in the PBMT1 was epithelial-like, whereas the PBMT2 leads to CSs with fusiform cells arranged in bundles. TEM identified a more mature ECM and signs of apoptosis and necrosis in the PBMT2 group. PBMT influence the composition and ultrastructure of the ECM of CSs of hDPSCs. Thus, PBMT, specifically when applied in the lower energy density, could be of importance in the determination of the mechanical quality of CSs, which may favor cell therapy by improving the CS transplantation approach. [Display omitted] •Photobiomodulation therapy (PBMT) is able to improve the characteristics of the cell sheet (CS).•PBMT improved extracellular matrix maturation in CSs, which could facilitate the procedures of cell transplantation.•Fibronectin synthesis was increased by PBMT.•Fibronectin possibly influenced the epithelial-like differentiation of the human dental pulp stem cells (hDPSCs) in the CSs.•PBMT applied with the parameter of 5 J/cm2 induced damage to the hDPSCs in the CSs.</abstract><cop>Switzerland</cop><pub>Elsevier B.V</pub><pmid>30954874</pmid><doi>10.1016/j.jphotobiol.2019.03.017</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-8571-7144</orcidid></addata></record>
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subjects Apoptosis
Ascorbic acid
Cell sheet
Collagen
Collagen (type I)
Composition
Continuous radiation
Density
Dental materials
Dental pulp
Dental pulp stem cells
Energy
Extracellular matrix
Fibronectin
Flow cytometry
Flux density
Histology
Immunohistochemistry
Mechanical properties
Mesenchyme
Microscopy
Necrosis
Photobiomodulation therapy
Protein composition
Regeneration
Scanning electron microscopy
Scanning transmission electron microscopy
Semiconductor lasers
Stem cells
Therapy
Tissue engineering
Transmission electron microscopy
Transplantation
Ultrastructure
Vitamin C
Western blotting
title Effects of photobiomodulation therapy on the extracellular matrix of human dental pulp cell sheets
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