Rutin promotes osteogenic differentiation of periodontal ligament stem cells through the GPR30-mediated PI3K/AKT/mTOR signaling pathway

Rutin is one of the flavonoids found in fruits and vegetables. Recent reports have revealed that rutin is a major player in proliferation and bone development. However, data on how rutin regulates the proliferation of periodontal ligament stem cells (PDLSCs), as well as the differentiation of osteog...

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Veröffentlicht in:Experimental biology and medicine (Maywood, N.J.) N.J.), 2020-03, Vol.245 (6), p.552-561, Article 1535370220903463
Hauptverfasser: Zhao, Bin, Xiong, Yixuan, Zhang, Yunpeng, Jia, Linglu, Zhang, Wenjing, Xu, Xin
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container_title Experimental biology and medicine (Maywood, N.J.)
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creator Zhao, Bin
Xiong, Yixuan
Zhang, Yunpeng
Jia, Linglu
Zhang, Wenjing
Xu, Xin
description Rutin is one of the flavonoids found in fruits and vegetables. Recent reports have revealed that rutin is a major player in proliferation and bone development. However, data on how rutin regulates the proliferation of periodontal ligament stem cells (PDLSCs), as well as the differentiation of osteogenic cells are scanty. Here, our findings showed that rutin enhanced PDLSCs proliferation, increased ALP activity, and matrix mineralization. Moreover, rutin significantly promoted the expression of osteogenic genes and elevated phosphorylated AKT and mTOR. Treatment with LY294002 reversed these effects by inhibiting PI3K. We also found that the expression levels of GPR30 were increased by rutin. Interestingly, this upregulation was not altered after the addition of LY294002. In addition, G15, a selective antagonist of GPR30, could reduce the beneficial effects induced by rutin and interfere with the modulation of PI3K/AKT/mTOR signal transduction. Collectively, our findings revealed that rutin increased proliferation and osteogenic differentiation of PDLSCs through GPR30-mediated PI3K/AKT/mTOR signal transduction. Therefore, it could be deduced that rutin as a certain flavonoid possesses therapeutic value for periodontal bone regeneration and tissue engineering. Impact statement In our study, the effects and mechanisms of rutin on the osteogenic differentiation and proliferation of PDLSCs were investigated. Our findings might provide basic knowledge and guidance to understand and use rutin in the bioengineering of the periodontal tissues and regeneration of bones. The following is a short description of the main findings: rutin promotes the osteogenic differentiation and proliferation of PDLSCs; PI3K/AKT/mTOR signal pathway mediates the effects of rutin on PDLSCs; rutin activates PI3K/AKT/mTOR signal pathway via GPR30.
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Recent reports have revealed that rutin is a major player in proliferation and bone development. However, data on how rutin regulates the proliferation of periodontal ligament stem cells (PDLSCs), as well as the differentiation of osteogenic cells are scanty. Here, our findings showed that rutin enhanced PDLSCs proliferation, increased ALP activity, and matrix mineralization. Moreover, rutin significantly promoted the expression of osteogenic genes and elevated phosphorylated AKT and mTOR. Treatment with LY294002 reversed these effects by inhibiting PI3K. We also found that the expression levels of GPR30 were increased by rutin. Interestingly, this upregulation was not altered after the addition of LY294002. In addition, G15, a selective antagonist of GPR30, could reduce the beneficial effects induced by rutin and interfere with the modulation of PI3K/AKT/mTOR signal transduction. Collectively, our findings revealed that rutin increased proliferation and osteogenic differentiation of PDLSCs through GPR30-mediated PI3K/AKT/mTOR signal transduction. Therefore, it could be deduced that rutin as a certain flavonoid possesses therapeutic value for periodontal bone regeneration and tissue engineering. Impact statement In our study, the effects and mechanisms of rutin on the osteogenic differentiation and proliferation of PDLSCs were investigated. Our findings might provide basic knowledge and guidance to understand and use rutin in the bioengineering of the periodontal tissues and regeneration of bones. The following is a short description of the main findings: rutin promotes the osteogenic differentiation and proliferation of PDLSCs; PI3K/AKT/mTOR signal pathway mediates the effects of rutin on PDLSCs; rutin activates PI3K/AKT/mTOR signal pathway via GPR30.</description><identifier>ISSN: 1535-3702</identifier><identifier>EISSN: 1535-3699</identifier><identifier>DOI: 10.1177/1535370220903463</identifier><identifier>PMID: 32036685</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Cell Differentiation ; Cells, Cultured ; Chromones - pharmacology ; Humans ; Induced Pluripotent Stem Cells - cytology ; Induced Pluripotent Stem Cells - drug effects ; Induced Pluripotent Stem Cells - metabolism ; Life Sciences &amp; Biomedicine ; Medicine, Research &amp; Experimental ; Morpholines - pharmacology ; Original Research ; Osteoblasts - cytology ; Osteoblasts - drug effects ; Osteoblasts - metabolism ; Osteogenesis ; Periodontal Ligament - cytology ; Phosphatidylinositol 3-Kinases - metabolism ; Protein Kinase Inhibitors - pharmacology ; Proto-Oncogene Proteins c-akt - metabolism ; Receptors, Estrogen - metabolism ; Receptors, G-Protein-Coupled - metabolism ; Research &amp; Experimental Medicine ; Rutin - pharmacology ; Science &amp; Technology ; Signal Transduction ; TOR Serine-Threonine Kinases - metabolism</subject><ispartof>Experimental biology and medicine (Maywood, N.J.), 2020-03, Vol.245 (6), p.552-561, Article 1535370220903463</ispartof><rights>2020 by the Society for Experimental Biology and Medicine</rights><rights>2020 by the Society for Experimental Biology and Medicine 2020 The Society for Experimental Biology and Medicine</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>38</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000512624500001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c500t-f6b5b3b66547cc8a074d58604eb083ad95401051462a1520a429fbd136d908f93</citedby><cites>FETCH-LOGICAL-c500t-f6b5b3b66547cc8a074d58604eb083ad95401051462a1520a429fbd136d908f93</cites><orcidid>0000-0002-5385-6115 ; 0000-0003-3547-9720</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158599/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158599/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,729,782,786,887,21828,27933,27934,28257,43630,43631,53800,53802</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32036685$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhao, Bin</creatorcontrib><creatorcontrib>Xiong, Yixuan</creatorcontrib><creatorcontrib>Zhang, Yunpeng</creatorcontrib><creatorcontrib>Jia, Linglu</creatorcontrib><creatorcontrib>Zhang, Wenjing</creatorcontrib><creatorcontrib>Xu, Xin</creatorcontrib><title>Rutin promotes osteogenic differentiation of periodontal ligament stem cells through the GPR30-mediated PI3K/AKT/mTOR signaling pathway</title><title>Experimental biology and medicine (Maywood, N.J.)</title><addtitle>EXP BIOL MED</addtitle><addtitle>Exp Biol Med (Maywood)</addtitle><description>Rutin is one of the flavonoids found in fruits and vegetables. Recent reports have revealed that rutin is a major player in proliferation and bone development. However, data on how rutin regulates the proliferation of periodontal ligament stem cells (PDLSCs), as well as the differentiation of osteogenic cells are scanty. Here, our findings showed that rutin enhanced PDLSCs proliferation, increased ALP activity, and matrix mineralization. Moreover, rutin significantly promoted the expression of osteogenic genes and elevated phosphorylated AKT and mTOR. Treatment with LY294002 reversed these effects by inhibiting PI3K. We also found that the expression levels of GPR30 were increased by rutin. Interestingly, this upregulation was not altered after the addition of LY294002. In addition, G15, a selective antagonist of GPR30, could reduce the beneficial effects induced by rutin and interfere with the modulation of PI3K/AKT/mTOR signal transduction. Collectively, our findings revealed that rutin increased proliferation and osteogenic differentiation of PDLSCs through GPR30-mediated PI3K/AKT/mTOR signal transduction. Therefore, it could be deduced that rutin as a certain flavonoid possesses therapeutic value for periodontal bone regeneration and tissue engineering. Impact statement In our study, the effects and mechanisms of rutin on the osteogenic differentiation and proliferation of PDLSCs were investigated. Our findings might provide basic knowledge and guidance to understand and use rutin in the bioengineering of the periodontal tissues and regeneration of bones. 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Experimental Medicine</topic><topic>Rutin - pharmacology</topic><topic>Science &amp; Technology</topic><topic>Signal Transduction</topic><topic>TOR Serine-Threonine Kinases - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Bin</creatorcontrib><creatorcontrib>Xiong, Yixuan</creatorcontrib><creatorcontrib>Zhang, Yunpeng</creatorcontrib><creatorcontrib>Jia, Linglu</creatorcontrib><creatorcontrib>Zhang, Wenjing</creatorcontrib><creatorcontrib>Xu, Xin</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Bin</au><au>Xiong, Yixuan</au><au>Zhang, Yunpeng</au><au>Jia, Linglu</au><au>Zhang, Wenjing</au><au>Xu, Xin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rutin promotes osteogenic differentiation of periodontal ligament stem cells through the GPR30-mediated PI3K/AKT/mTOR signaling pathway</atitle><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle><stitle>EXP BIOL MED</stitle><addtitle>Exp Biol Med (Maywood)</addtitle><date>2020-03-01</date><risdate>2020</risdate><volume>245</volume><issue>6</issue><spage>552</spage><epage>561</epage><pages>552-561</pages><artnum>1535370220903463</artnum><issn>1535-3702</issn><eissn>1535-3699</eissn><abstract>Rutin is one of the flavonoids found in fruits and vegetables. Recent reports have revealed that rutin is a major player in proliferation and bone development. However, data on how rutin regulates the proliferation of periodontal ligament stem cells (PDLSCs), as well as the differentiation of osteogenic cells are scanty. Here, our findings showed that rutin enhanced PDLSCs proliferation, increased ALP activity, and matrix mineralization. Moreover, rutin significantly promoted the expression of osteogenic genes and elevated phosphorylated AKT and mTOR. Treatment with LY294002 reversed these effects by inhibiting PI3K. We also found that the expression levels of GPR30 were increased by rutin. Interestingly, this upregulation was not altered after the addition of LY294002. In addition, G15, a selective antagonist of GPR30, could reduce the beneficial effects induced by rutin and interfere with the modulation of PI3K/AKT/mTOR signal transduction. Collectively, our findings revealed that rutin increased proliferation and osteogenic differentiation of PDLSCs through GPR30-mediated PI3K/AKT/mTOR signal transduction. Therefore, it could be deduced that rutin as a certain flavonoid possesses therapeutic value for periodontal bone regeneration and tissue engineering. Impact statement In our study, the effects and mechanisms of rutin on the osteogenic differentiation and proliferation of PDLSCs were investigated. Our findings might provide basic knowledge and guidance to understand and use rutin in the bioengineering of the periodontal tissues and regeneration of bones. The following is a short description of the main findings: rutin promotes the osteogenic differentiation and proliferation of PDLSCs; PI3K/AKT/mTOR signal pathway mediates the effects of rutin on PDLSCs; rutin activates PI3K/AKT/mTOR signal pathway via GPR30.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>32036685</pmid><doi>10.1177/1535370220903463</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-5385-6115</orcidid><orcidid>https://orcid.org/0000-0003-3547-9720</orcidid><oa>free_for_read</oa></addata></record>
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subjects Cell Differentiation
Cells, Cultured
Chromones - pharmacology
Humans
Induced Pluripotent Stem Cells - cytology
Induced Pluripotent Stem Cells - drug effects
Induced Pluripotent Stem Cells - metabolism
Life Sciences & Biomedicine
Medicine, Research & Experimental
Morpholines - pharmacology
Original Research
Osteoblasts - cytology
Osteoblasts - drug effects
Osteoblasts - metabolism
Osteogenesis
Periodontal Ligament - cytology
Phosphatidylinositol 3-Kinases - metabolism
Protein Kinase Inhibitors - pharmacology
Proto-Oncogene Proteins c-akt - metabolism
Receptors, Estrogen - metabolism
Receptors, G-Protein-Coupled - metabolism
Research & Experimental Medicine
Rutin - pharmacology
Science & Technology
Signal Transduction
TOR Serine-Threonine Kinases - metabolism
title Rutin promotes osteogenic differentiation of periodontal ligament stem cells through the GPR30-mediated PI3K/AKT/mTOR signaling pathway
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