Combined application of geranylgeranylacetone and amelogenin promotes angiogenesis and wound healing in human periodontal ligament cells
Amelogenin directly binds to glucose‐regulated protein 78 (Grp78). Cell migration activity is expected to increase when human periodontal ligament cells (hPDLCs) overexpressing Grp78 are treated with amelogenin. Geranylgeranylacetone (GGA) is a drug that induces the expression of heat shock protein...
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Veröffentlicht in: | Journal of cellular biochemistry 2021-07, Vol.122 (7), p.716-730 |
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creator | Yamato, Hiroaki Sanui, Terukazu Yotsumoto, Karen Nakao, Yuki Watanabe, Yukari Hayashi, Chikako Aihara, Ryosuke Iwashita, Misaki Tanaka, Urara Taketomi, Takaharu Fukuda, Takao Nishimura, Fusanori |
description | Amelogenin directly binds to glucose‐regulated protein 78 (Grp78). Cell migration activity is expected to increase when human periodontal ligament cells (hPDLCs) overexpressing Grp78 are treated with amelogenin. Geranylgeranylacetone (GGA) is a drug that induces the expression of heat shock protein and is routinely used to treat gastric ulcers. Here, we investigated the changes in the properties and behavior of hPDLCs in response to treatment with GGA and the synergistic effects of amelogenin stimulation in hPDLCs pretreated with GGA for the establishment of a novel periodontal tissue regenerative therapy. We observed that GGA treatment increased Grp78 protein expression in hPDLCs and enhanced cell migration. Microarray analysis demonstrated that increased Grp78 expression triggered the production of angiopoietin‐like 4 and amphiregulin, which are involved in the enhancement of angiogenesis and subsequent wound healing via the activation of hypoxia‐inducible factor 1α and peroxisome proliferator‐activated receptors as well as the phosphorylation of cAMP response element‐binding protein and protein kinase A. Moreover, the addition of recombinant murine amelogenin (rM180) further accelerated hPDLC migration and tube formation of human umbilical vein endothelial cells due to the upregulation of interleukin‐8 (IL‐8), monocyte chemotactic protein 1, and IL‐6, which are also known as angiogenesis‐inducing factors. These findings suggest that the application of GGA to gingival tissue and alveolar bone damaged by periodontal disease would facilitate the wound healing process by inducing periodontal ligament cells to migrate to the root surface and release cytokines involved in tissue repair. Additionally, supplementation with amelogenin synergistically enhanced the migratory capacity of these cells while actively promoting angiogenesis. Therefore, the combined application of GGA and amelogenin may establish a suitable environment for periodontal wound healing and further drive the development of novel therapeutics for periodontal tissue regeneration.
Our study demonstrated that geranylgeranylacetone (GGA) increases glucose‐regulated protein 78 (Grp78) expression and enhances the migration of human periodontal ligament cells (hPDLCs). Also, this increased Grp78 expression triggers the production of Angptl4 and Areg, which are involved in angiogenesis and wound healing, via the activation of hypoxia‐inducible factor 1α (HIF‐1α) and peroxisome proliferator‐activated |
doi_str_mv | 10.1002/jcb.29903 |
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Our study demonstrated that geranylgeranylacetone (GGA) increases glucose‐regulated protein 78 (Grp78) expression and enhances the migration of human periodontal ligament cells (hPDLCs). Also, this increased Grp78 expression triggers the production of Angptl4 and Areg, which are involved in angiogenesis and wound healing, via the activation of hypoxia‐inducible factor 1α (HIF‐1α) and peroxisome proliferator‐activated receptor δ (PPARδ) and the phosphorylation of CREB and PKA. In addition, supplementation with rM180 amelogenin not only strongly enhances the migratory capacity of hPDLCs, but also accelerates their angiogenic activity due to the upregulation of the interleukin‐8 (IL‐8), monocyte chemotactic protein 1 (MCP‐1), and IL‐6.</description><identifier>ISSN: 0730-2312</identifier><identifier>EISSN: 1097-4644</identifier><identifier>DOI: 10.1002/jcb.29903</identifier><identifier>PMID: 33529434</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Alveolar bone ; Amelogenin ; Amphiregulin ; Angiogenesis ; Angiopoietin ; Bone healing ; Cell adhesion & migration ; Cytokines ; Drug development ; Endothelial cells ; geranylgeranylacetone ; GRP78 protein ; Heat shock proteins ; Hypoxia ; Interleukins ; Kinases ; Leukocyte migration ; Ligaments ; migration ; Monocyte chemoattractant protein 1 ; Monocytes ; Periodontal disease ; Periodontal diseases ; Periodontal ligament ; periodontal ligament cells ; Phosphorylation ; Protein kinase A ; Proteins ; Regeneration ; Supplements ; Synergistic effect ; Tissue engineering ; Tissues ; Ulcers ; Umbilical vein ; Wound healing</subject><ispartof>Journal of cellular biochemistry, 2021-07, Vol.122 (7), p.716-730</ispartof><rights>2021 Wiley Periodicals LLC</rights><rights>2021 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5823-e22e90d4f069c5b95b8f5fc44d1c9913a6026137cad4455ea67ed088bb91ebf3</citedby><cites>FETCH-LOGICAL-c5823-e22e90d4f069c5b95b8f5fc44d1c9913a6026137cad4455ea67ed088bb91ebf3</cites><orcidid>0000-0003-1572-2180 ; 0000-0002-5249-9574 ; 0000-0002-6002-5512 ; 0000-0003-0430-1874</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcb.29903$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcb.29903$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33529434$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamato, Hiroaki</creatorcontrib><creatorcontrib>Sanui, Terukazu</creatorcontrib><creatorcontrib>Yotsumoto, Karen</creatorcontrib><creatorcontrib>Nakao, Yuki</creatorcontrib><creatorcontrib>Watanabe, Yukari</creatorcontrib><creatorcontrib>Hayashi, Chikako</creatorcontrib><creatorcontrib>Aihara, Ryosuke</creatorcontrib><creatorcontrib>Iwashita, Misaki</creatorcontrib><creatorcontrib>Tanaka, Urara</creatorcontrib><creatorcontrib>Taketomi, Takaharu</creatorcontrib><creatorcontrib>Fukuda, Takao</creatorcontrib><creatorcontrib>Nishimura, Fusanori</creatorcontrib><title>Combined application of geranylgeranylacetone and amelogenin promotes angiogenesis and wound healing in human periodontal ligament cells</title><title>Journal of cellular biochemistry</title><addtitle>J Cell Biochem</addtitle><description>Amelogenin directly binds to glucose‐regulated protein 78 (Grp78). Cell migration activity is expected to increase when human periodontal ligament cells (hPDLCs) overexpressing Grp78 are treated with amelogenin. Geranylgeranylacetone (GGA) is a drug that induces the expression of heat shock protein and is routinely used to treat gastric ulcers. Here, we investigated the changes in the properties and behavior of hPDLCs in response to treatment with GGA and the synergistic effects of amelogenin stimulation in hPDLCs pretreated with GGA for the establishment of a novel periodontal tissue regenerative therapy. We observed that GGA treatment increased Grp78 protein expression in hPDLCs and enhanced cell migration. Microarray analysis demonstrated that increased Grp78 expression triggered the production of angiopoietin‐like 4 and amphiregulin, which are involved in the enhancement of angiogenesis and subsequent wound healing via the activation of hypoxia‐inducible factor 1α and peroxisome proliferator‐activated receptors as well as the phosphorylation of cAMP response element‐binding protein and protein kinase A. Moreover, the addition of recombinant murine amelogenin (rM180) further accelerated hPDLC migration and tube formation of human umbilical vein endothelial cells due to the upregulation of interleukin‐8 (IL‐8), monocyte chemotactic protein 1, and IL‐6, which are also known as angiogenesis‐inducing factors. These findings suggest that the application of GGA to gingival tissue and alveolar bone damaged by periodontal disease would facilitate the wound healing process by inducing periodontal ligament cells to migrate to the root surface and release cytokines involved in tissue repair. Additionally, supplementation with amelogenin synergistically enhanced the migratory capacity of these cells while actively promoting angiogenesis. Therefore, the combined application of GGA and amelogenin may establish a suitable environment for periodontal wound healing and further drive the development of novel therapeutics for periodontal tissue regeneration.
Our study demonstrated that geranylgeranylacetone (GGA) increases glucose‐regulated protein 78 (Grp78) expression and enhances the migration of human periodontal ligament cells (hPDLCs). Also, this increased Grp78 expression triggers the production of Angptl4 and Areg, which are involved in angiogenesis and wound healing, via the activation of hypoxia‐inducible factor 1α (HIF‐1α) and peroxisome proliferator‐activated receptor δ (PPARδ) and the phosphorylation of CREB and PKA. In addition, supplementation with rM180 amelogenin not only strongly enhances the migratory capacity of hPDLCs, but also accelerates their angiogenic activity due to the upregulation of the interleukin‐8 (IL‐8), monocyte chemotactic protein 1 (MCP‐1), and IL‐6.</description><subject>Alveolar bone</subject><subject>Amelogenin</subject><subject>Amphiregulin</subject><subject>Angiogenesis</subject><subject>Angiopoietin</subject><subject>Bone healing</subject><subject>Cell adhesion & migration</subject><subject>Cytokines</subject><subject>Drug development</subject><subject>Endothelial cells</subject><subject>geranylgeranylacetone</subject><subject>GRP78 protein</subject><subject>Heat shock proteins</subject><subject>Hypoxia</subject><subject>Interleukins</subject><subject>Kinases</subject><subject>Leukocyte migration</subject><subject>Ligaments</subject><subject>migration</subject><subject>Monocyte chemoattractant protein 1</subject><subject>Monocytes</subject><subject>Periodontal disease</subject><subject>Periodontal diseases</subject><subject>Periodontal ligament</subject><subject>periodontal ligament cells</subject><subject>Phosphorylation</subject><subject>Protein kinase A</subject><subject>Proteins</subject><subject>Regeneration</subject><subject>Supplements</subject><subject>Synergistic effect</subject><subject>Tissue engineering</subject><subject>Tissues</subject><subject>Ulcers</subject><subject>Umbilical vein</subject><subject>Wound healing</subject><issn>0730-2312</issn><issn>1097-4644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kc1qGzEURkVJqB23i75AGcimWYyjf4-WjWnahEA22QuN5s5YRiO5oxmM3yCPHTl2uyh0owuXo8PH_RD6QvCSYExvt7ZeUqUw-4DmBKtVySXnF2iOVwyXlBE6Q1cpbTHGSjH6Ec0YE1RxxufodR372gVoCrPbeWfN6GIoYlt0MJhw8OdhLIwxQGFCBnvwsYPgQrEbYh9HSHnfueMOkkvv0D5O-d2A8S50RUY3U2_yBxhcbGIYjS-867IqjIUF79MndNkan-DzeS7Qy_2Pl_Wv8un558P6-1NpRUVZCZSCwg1vsVRW1ErUVStay3lDrFKEGYmpJGxlTcO5EGDkChpcVXWtCNQtW6BvJ22O_nuCNOrepWMAEyBOSVNeScIFpVVGr_9Bt3EaQg6nqaBSVkTmky_QzYmyQ0xpgFbvBteb4aAJ1sd2dG5Hv7eT2a9n41T30Pwl_9SRgdsTsHceDv836cf13Un5Blt7m70</recordid><startdate>202107</startdate><enddate>202107</enddate><creator>Yamato, Hiroaki</creator><creator>Sanui, Terukazu</creator><creator>Yotsumoto, Karen</creator><creator>Nakao, Yuki</creator><creator>Watanabe, Yukari</creator><creator>Hayashi, Chikako</creator><creator>Aihara, Ryosuke</creator><creator>Iwashita, Misaki</creator><creator>Tanaka, Urara</creator><creator>Taketomi, Takaharu</creator><creator>Fukuda, Takao</creator><creator>Nishimura, Fusanori</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1572-2180</orcidid><orcidid>https://orcid.org/0000-0002-5249-9574</orcidid><orcidid>https://orcid.org/0000-0002-6002-5512</orcidid><orcidid>https://orcid.org/0000-0003-0430-1874</orcidid></search><sort><creationdate>202107</creationdate><title>Combined application of geranylgeranylacetone and amelogenin promotes angiogenesis and wound healing in human periodontal ligament cells</title><author>Yamato, Hiroaki ; Sanui, Terukazu ; Yotsumoto, Karen ; Nakao, Yuki ; Watanabe, Yukari ; Hayashi, Chikako ; Aihara, Ryosuke ; Iwashita, Misaki ; Tanaka, Urara ; Taketomi, Takaharu ; Fukuda, Takao ; Nishimura, Fusanori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5823-e22e90d4f069c5b95b8f5fc44d1c9913a6026137cad4455ea67ed088bb91ebf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alveolar bone</topic><topic>Amelogenin</topic><topic>Amphiregulin</topic><topic>Angiogenesis</topic><topic>Angiopoietin</topic><topic>Bone healing</topic><topic>Cell adhesion & migration</topic><topic>Cytokines</topic><topic>Drug development</topic><topic>Endothelial cells</topic><topic>geranylgeranylacetone</topic><topic>GRP78 protein</topic><topic>Heat shock proteins</topic><topic>Hypoxia</topic><topic>Interleukins</topic><topic>Kinases</topic><topic>Leukocyte migration</topic><topic>Ligaments</topic><topic>migration</topic><topic>Monocyte chemoattractant protein 1</topic><topic>Monocytes</topic><topic>Periodontal disease</topic><topic>Periodontal diseases</topic><topic>Periodontal ligament</topic><topic>periodontal ligament cells</topic><topic>Phosphorylation</topic><topic>Protein kinase A</topic><topic>Proteins</topic><topic>Regeneration</topic><topic>Supplements</topic><topic>Synergistic effect</topic><topic>Tissue engineering</topic><topic>Tissues</topic><topic>Ulcers</topic><topic>Umbilical vein</topic><topic>Wound healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamato, Hiroaki</creatorcontrib><creatorcontrib>Sanui, Terukazu</creatorcontrib><creatorcontrib>Yotsumoto, Karen</creatorcontrib><creatorcontrib>Nakao, Yuki</creatorcontrib><creatorcontrib>Watanabe, Yukari</creatorcontrib><creatorcontrib>Hayashi, Chikako</creatorcontrib><creatorcontrib>Aihara, Ryosuke</creatorcontrib><creatorcontrib>Iwashita, Misaki</creatorcontrib><creatorcontrib>Tanaka, Urara</creatorcontrib><creatorcontrib>Taketomi, Takaharu</creatorcontrib><creatorcontrib>Fukuda, Takao</creatorcontrib><creatorcontrib>Nishimura, Fusanori</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamato, Hiroaki</au><au>Sanui, Terukazu</au><au>Yotsumoto, Karen</au><au>Nakao, Yuki</au><au>Watanabe, Yukari</au><au>Hayashi, Chikako</au><au>Aihara, Ryosuke</au><au>Iwashita, Misaki</au><au>Tanaka, Urara</au><au>Taketomi, Takaharu</au><au>Fukuda, Takao</au><au>Nishimura, Fusanori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combined application of geranylgeranylacetone and amelogenin promotes angiogenesis and wound healing in human periodontal ligament cells</atitle><jtitle>Journal of cellular biochemistry</jtitle><addtitle>J Cell Biochem</addtitle><date>2021-07</date><risdate>2021</risdate><volume>122</volume><issue>7</issue><spage>716</spage><epage>730</epage><pages>716-730</pages><issn>0730-2312</issn><eissn>1097-4644</eissn><abstract>Amelogenin directly binds to glucose‐regulated protein 78 (Grp78). Cell migration activity is expected to increase when human periodontal ligament cells (hPDLCs) overexpressing Grp78 are treated with amelogenin. Geranylgeranylacetone (GGA) is a drug that induces the expression of heat shock protein and is routinely used to treat gastric ulcers. Here, we investigated the changes in the properties and behavior of hPDLCs in response to treatment with GGA and the synergistic effects of amelogenin stimulation in hPDLCs pretreated with GGA for the establishment of a novel periodontal tissue regenerative therapy. We observed that GGA treatment increased Grp78 protein expression in hPDLCs and enhanced cell migration. Microarray analysis demonstrated that increased Grp78 expression triggered the production of angiopoietin‐like 4 and amphiregulin, which are involved in the enhancement of angiogenesis and subsequent wound healing via the activation of hypoxia‐inducible factor 1α and peroxisome proliferator‐activated receptors as well as the phosphorylation of cAMP response element‐binding protein and protein kinase A. Moreover, the addition of recombinant murine amelogenin (rM180) further accelerated hPDLC migration and tube formation of human umbilical vein endothelial cells due to the upregulation of interleukin‐8 (IL‐8), monocyte chemotactic protein 1, and IL‐6, which are also known as angiogenesis‐inducing factors. These findings suggest that the application of GGA to gingival tissue and alveolar bone damaged by periodontal disease would facilitate the wound healing process by inducing periodontal ligament cells to migrate to the root surface and release cytokines involved in tissue repair. Additionally, supplementation with amelogenin synergistically enhanced the migratory capacity of these cells while actively promoting angiogenesis. Therefore, the combined application of GGA and amelogenin may establish a suitable environment for periodontal wound healing and further drive the development of novel therapeutics for periodontal tissue regeneration.
Our study demonstrated that geranylgeranylacetone (GGA) increases glucose‐regulated protein 78 (Grp78) expression and enhances the migration of human periodontal ligament cells (hPDLCs). Also, this increased Grp78 expression triggers the production of Angptl4 and Areg, which are involved in angiogenesis and wound healing, via the activation of hypoxia‐inducible factor 1α (HIF‐1α) and peroxisome proliferator‐activated receptor δ (PPARδ) and the phosphorylation of CREB and PKA. In addition, supplementation with rM180 amelogenin not only strongly enhances the migratory capacity of hPDLCs, but also accelerates their angiogenic activity due to the upregulation of the interleukin‐8 (IL‐8), monocyte chemotactic protein 1 (MCP‐1), and IL‐6.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33529434</pmid><doi>10.1002/jcb.29903</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-1572-2180</orcidid><orcidid>https://orcid.org/0000-0002-5249-9574</orcidid><orcidid>https://orcid.org/0000-0002-6002-5512</orcidid><orcidid>https://orcid.org/0000-0003-0430-1874</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alveolar bone Amelogenin Amphiregulin Angiogenesis Angiopoietin Bone healing Cell adhesion & migration Cytokines Drug development Endothelial cells geranylgeranylacetone GRP78 protein Heat shock proteins Hypoxia Interleukins Kinases Leukocyte migration Ligaments migration Monocyte chemoattractant protein 1 Monocytes Periodontal disease Periodontal diseases Periodontal ligament periodontal ligament cells Phosphorylation Protein kinase A Proteins Regeneration Supplements Synergistic effect Tissue engineering Tissues Ulcers Umbilical vein Wound healing |
title | Combined application of geranylgeranylacetone and amelogenin promotes angiogenesis and wound healing in human periodontal ligament cells |
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