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Similar in vitro effects and pulp regeneration in ectopic tooth transplantation by basic fibroblast growth factor and granulocyte-colony stimulating factor
Objectives Granulocyte‐colony stimulating factor (G‐CSF) has been shown to have combinatorial trophic effects with dental pulp stem cells for pulp regeneration. The aim of this investigation is to examine the effects of basic fibroblast growth factor (bFGF) in vitro and in vivo compared with those o...
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Published in: | Oral diseases 2015-01, Vol.21 (1), p.113-122 |
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container_title | Oral diseases |
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creator | Takeuchi, N Hayashi, Y Murakami, M Alvarez, FJ Horibe, H Iohara, K Nakata, K Nakamura, H Nakashima, M |
description | Objectives
Granulocyte‐colony stimulating factor (G‐CSF) has been shown to have combinatorial trophic effects with dental pulp stem cells for pulp regeneration. The aim of this investigation is to examine the effects of basic fibroblast growth factor (bFGF) in vitro and in vivo compared with those of G‐CSF and to assess the potential utility of bFGF as an alternative to G‐CSF for pulp regeneration.
Materials and methods
Five different types of cells were examined in the in vitro effects of bFGF on cell migration, proliferation, anti‐apoptosis, neurite outgrowth, angiogenesis, and odontogenesis compared with those of G‐CSF. The in vivo regenerative potential of pulp tissue including vasculogenesis and odontoblastic differentiation was also compared using an ectopic tooth transplantation model.
Results
Basic fibroblast growth factor was similar to G‐CSF in high migration, proliferation and anti‐apoptotic effects and angiogenic and neurite outgrowth stimulatory activities in vitro. There was no significant difference between bFGF and G‐CSF in the regenerative potential in vivo.
Conclusions
The potential utility of bFGF for pulp regeneration is demonstrated as a homing/migration factor similar to the influence of G‐CSF. |
doi_str_mv | 10.1111/odi.12227 |
format | article |
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Granulocyte‐colony stimulating factor (G‐CSF) has been shown to have combinatorial trophic effects with dental pulp stem cells for pulp regeneration. The aim of this investigation is to examine the effects of basic fibroblast growth factor (bFGF) in vitro and in vivo compared with those of G‐CSF and to assess the potential utility of bFGF as an alternative to G‐CSF for pulp regeneration.
Materials and methods
Five different types of cells were examined in the in vitro effects of bFGF on cell migration, proliferation, anti‐apoptosis, neurite outgrowth, angiogenesis, and odontogenesis compared with those of G‐CSF. The in vivo regenerative potential of pulp tissue including vasculogenesis and odontoblastic differentiation was also compared using an ectopic tooth transplantation model.
Results
Basic fibroblast growth factor was similar to G‐CSF in high migration, proliferation and anti‐apoptotic effects and angiogenic and neurite outgrowth stimulatory activities in vitro. There was no significant difference between bFGF and G‐CSF in the regenerative potential in vivo.
Conclusions
The potential utility of bFGF for pulp regeneration is demonstrated as a homing/migration factor similar to the influence of G‐CSF.</description><identifier>ISSN: 1354-523X</identifier><identifier>EISSN: 1601-0825</identifier><identifier>DOI: 10.1111/odi.12227</identifier><identifier>PMID: 24495211</identifier><language>eng</language><publisher>Denmark: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Animals ; Apoptosis - drug effects ; Apoptosis - physiology ; basic fibroblast growth factor ; Cell adhesion & migration ; Cell Movement - drug effects ; Cell Movement - physiology ; Cell Proliferation - drug effects ; Cell Proliferation - physiology ; Dental Pulp - drug effects ; Dental Pulp - physiology ; Dentistry ; Fibroblast Growth Factor 2 - pharmacology ; Granulocyte Colony-Stimulating Factor - pharmacology ; granulocyte-colony stimulating factor ; homing/migration factor ; Humans ; In Vitro Techniques ; Medical research ; Mice ; Mice, SCID ; Molar - physiology ; Molar - transplantation ; Neovascularization, Physiologic - drug effects ; Neovascularization, Physiologic - physiology ; Odontogenesis - drug effects ; Odontogenesis - physiology ; Oral diseases ; pulp regeneration ; Swine ; Young Adult</subject><ispartof>Oral diseases, 2015-01, Vol.21 (1), p.113-122</ispartof><rights>2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5607-bf1440efaf6d2a7849ad75438522482aa0f671d13b727a9d2884cefdfeaa01b63</citedby><cites>FETCH-LOGICAL-c5607-bf1440efaf6d2a7849ad75438522482aa0f671d13b727a9d2884cefdfeaa01b63</cites><orcidid>0000-0003-2095-1324</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24495211$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takeuchi, N</creatorcontrib><creatorcontrib>Hayashi, Y</creatorcontrib><creatorcontrib>Murakami, M</creatorcontrib><creatorcontrib>Alvarez, FJ</creatorcontrib><creatorcontrib>Horibe, H</creatorcontrib><creatorcontrib>Iohara, K</creatorcontrib><creatorcontrib>Nakata, K</creatorcontrib><creatorcontrib>Nakamura, H</creatorcontrib><creatorcontrib>Nakashima, M</creatorcontrib><title>Similar in vitro effects and pulp regeneration in ectopic tooth transplantation by basic fibroblast growth factor and granulocyte-colony stimulating factor</title><title>Oral diseases</title><addtitle>Oral Dis</addtitle><description>Objectives
Granulocyte‐colony stimulating factor (G‐CSF) has been shown to have combinatorial trophic effects with dental pulp stem cells for pulp regeneration. The aim of this investigation is to examine the effects of basic fibroblast growth factor (bFGF) in vitro and in vivo compared with those of G‐CSF and to assess the potential utility of bFGF as an alternative to G‐CSF for pulp regeneration.
Materials and methods
Five different types of cells were examined in the in vitro effects of bFGF on cell migration, proliferation, anti‐apoptosis, neurite outgrowth, angiogenesis, and odontogenesis compared with those of G‐CSF. The in vivo regenerative potential of pulp tissue including vasculogenesis and odontoblastic differentiation was also compared using an ectopic tooth transplantation model.
Results
Basic fibroblast growth factor was similar to G‐CSF in high migration, proliferation and anti‐apoptotic effects and angiogenic and neurite outgrowth stimulatory activities in vitro. There was no significant difference between bFGF and G‐CSF in the regenerative potential in vivo.
Conclusions
The potential utility of bFGF for pulp regeneration is demonstrated as a homing/migration factor similar to the influence of G‐CSF.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Apoptosis - physiology</subject><subject>basic fibroblast growth factor</subject><subject>Cell adhesion & migration</subject><subject>Cell Movement - drug effects</subject><subject>Cell Movement - physiology</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Proliferation - physiology</subject><subject>Dental Pulp - drug effects</subject><subject>Dental Pulp - physiology</subject><subject>Dentistry</subject><subject>Fibroblast Growth Factor 2 - pharmacology</subject><subject>Granulocyte Colony-Stimulating Factor - pharmacology</subject><subject>granulocyte-colony stimulating factor</subject><subject>homing/migration factor</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Medical research</subject><subject>Mice</subject><subject>Mice, SCID</subject><subject>Molar - physiology</subject><subject>Molar - transplantation</subject><subject>Neovascularization, Physiologic - drug effects</subject><subject>Neovascularization, Physiologic - physiology</subject><subject>Odontogenesis - drug effects</subject><subject>Odontogenesis - physiology</subject><subject>Oral diseases</subject><subject>pulp regeneration</subject><subject>Swine</subject><subject>Young Adult</subject><issn>1354-523X</issn><issn>1601-0825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNkc9qFTEYxYNYbK0ufAEJuNHFtPk3ycxS2npbuLQLKxY3ITOTXFMzkzHJtM6z-LLmdm67EAQDIYHzO4fv4wDwBqMjnM-x7-wRJoSIZ-AAc4QLVJHyef7TkhUloTf74GWMtwhhUVPyAuwTxuqSYHwAfn-2vXUqQDvAO5uCh9oY3aYI1dDBcXIjDHqjBx1Usn7YYln1o21h8j59hymoIY5ODWkBmhk2KmbZ2Cb4xqmY4Cb4-4walZ3hIXiTXZPz7Zx00XrnhxnGZPvJ5ZBhsyNfgT2jXNSvd-8h-PLp7PrkvFhfrS5OPq6LtuRIFI3BjCFtlOEdUaJitepEyWhVEsIqohQyXOAO00YQoeqOVBVrtemMzhJuOD0E75fcMfifk45J9ja22uWltJ-ixLxkPF9C_wOldV0RRnFG3_2F3vopDHmRLZWnZIKjTH1YqDb4GIM2cgy2V2GWGMltuTKXKx_KzezbXeLU9Lp7Ih_bzMDxAtxbp-d_J8mr04vHyGJx2Jj0ryeHCj8kF1SU8uvlSrKby2-n19Varugf2WbAew</recordid><startdate>201501</startdate><enddate>201501</enddate><creator>Takeuchi, N</creator><creator>Hayashi, Y</creator><creator>Murakami, M</creator><creator>Alvarez, FJ</creator><creator>Horibe, H</creator><creator>Iohara, K</creator><creator>Nakata, K</creator><creator>Nakamura, H</creator><creator>Nakashima, M</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2095-1324</orcidid></search><sort><creationdate>201501</creationdate><title>Similar in vitro effects and pulp regeneration in ectopic tooth transplantation by basic fibroblast growth factor and granulocyte-colony stimulating factor</title><author>Takeuchi, N ; Hayashi, Y ; Murakami, M ; Alvarez, FJ ; Horibe, H ; Iohara, K ; Nakata, K ; Nakamura, H ; Nakashima, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5607-bf1440efaf6d2a7849ad75438522482aa0f671d13b727a9d2884cefdfeaa01b63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Apoptosis - physiology</topic><topic>basic fibroblast growth factor</topic><topic>Cell adhesion & migration</topic><topic>Cell Movement - drug effects</topic><topic>Cell Movement - physiology</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Proliferation - physiology</topic><topic>Dental Pulp - drug effects</topic><topic>Dental Pulp - physiology</topic><topic>Dentistry</topic><topic>Fibroblast Growth Factor 2 - pharmacology</topic><topic>Granulocyte Colony-Stimulating Factor - pharmacology</topic><topic>granulocyte-colony stimulating factor</topic><topic>homing/migration factor</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Medical research</topic><topic>Mice</topic><topic>Mice, SCID</topic><topic>Molar - physiology</topic><topic>Molar - transplantation</topic><topic>Neovascularization, Physiologic - drug effects</topic><topic>Neovascularization, Physiologic - physiology</topic><topic>Odontogenesis - drug effects</topic><topic>Odontogenesis - physiology</topic><topic>Oral diseases</topic><topic>pulp regeneration</topic><topic>Swine</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takeuchi, N</creatorcontrib><creatorcontrib>Hayashi, Y</creatorcontrib><creatorcontrib>Murakami, M</creatorcontrib><creatorcontrib>Alvarez, FJ</creatorcontrib><creatorcontrib>Horibe, H</creatorcontrib><creatorcontrib>Iohara, K</creatorcontrib><creatorcontrib>Nakata, K</creatorcontrib><creatorcontrib>Nakamura, H</creatorcontrib><creatorcontrib>Nakashima, M</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Oral diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takeuchi, N</au><au>Hayashi, Y</au><au>Murakami, M</au><au>Alvarez, FJ</au><au>Horibe, H</au><au>Iohara, K</au><au>Nakata, K</au><au>Nakamura, H</au><au>Nakashima, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Similar in vitro effects and pulp regeneration in ectopic tooth transplantation by basic fibroblast growth factor and granulocyte-colony stimulating factor</atitle><jtitle>Oral diseases</jtitle><addtitle>Oral Dis</addtitle><date>2015-01</date><risdate>2015</risdate><volume>21</volume><issue>1</issue><spage>113</spage><epage>122</epage><pages>113-122</pages><issn>1354-523X</issn><eissn>1601-0825</eissn><abstract>Objectives
Granulocyte‐colony stimulating factor (G‐CSF) has been shown to have combinatorial trophic effects with dental pulp stem cells for pulp regeneration. The aim of this investigation is to examine the effects of basic fibroblast growth factor (bFGF) in vitro and in vivo compared with those of G‐CSF and to assess the potential utility of bFGF as an alternative to G‐CSF for pulp regeneration.
Materials and methods
Five different types of cells were examined in the in vitro effects of bFGF on cell migration, proliferation, anti‐apoptosis, neurite outgrowth, angiogenesis, and odontogenesis compared with those of G‐CSF. The in vivo regenerative potential of pulp tissue including vasculogenesis and odontoblastic differentiation was also compared using an ectopic tooth transplantation model.
Results
Basic fibroblast growth factor was similar to G‐CSF in high migration, proliferation and anti‐apoptotic effects and angiogenic and neurite outgrowth stimulatory activities in vitro. There was no significant difference between bFGF and G‐CSF in the regenerative potential in vivo.
Conclusions
The potential utility of bFGF for pulp regeneration is demonstrated as a homing/migration factor similar to the influence of G‐CSF.</abstract><cop>Denmark</cop><pub>Blackwell Publishing Ltd</pub><pmid>24495211</pmid><doi>10.1111/odi.12227</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-2095-1324</orcidid></addata></record> |
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subjects | Adolescent Adult Animals Apoptosis - drug effects Apoptosis - physiology basic fibroblast growth factor Cell adhesion & migration Cell Movement - drug effects Cell Movement - physiology Cell Proliferation - drug effects Cell Proliferation - physiology Dental Pulp - drug effects Dental Pulp - physiology Dentistry Fibroblast Growth Factor 2 - pharmacology Granulocyte Colony-Stimulating Factor - pharmacology granulocyte-colony stimulating factor homing/migration factor Humans In Vitro Techniques Medical research Mice Mice, SCID Molar - physiology Molar - transplantation Neovascularization, Physiologic - drug effects Neovascularization, Physiologic - physiology Odontogenesis - drug effects Odontogenesis - physiology Oral diseases pulp regeneration Swine Young Adult |
title | Similar in vitro effects and pulp regeneration in ectopic tooth transplantation by basic fibroblast growth factor and granulocyte-colony stimulating factor |
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