Fibrocyte: A missing piece in the pathogenesis of fibrous epulis
Objectives To explore the role of fibrocytes in the recurrence and calcification of fibrous epulides. Methods Different subtypes of fibrous epulides and normal gingival tissue specimens were first collected for histological and immunofluorescence analyses to see if fibrocytes were present and whethe...
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Veröffentlicht in: | Oral diseases 2024-10, Vol.30 (7), p.4376-4389 |
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creator | Zhu, Yi‐fei Wan, Mei‐chen Gao, Peng Shen, Min‐juan Zhu, Yi‐na Hao, Jia‐xin Lu, Wei‐cheng Wang, Chen‐yu Tay, Franklin Ehrlich, Hermann Niu, Li‐na Jiao, Kai |
description | Objectives
To explore the role of fibrocytes in the recurrence and calcification of fibrous epulides.
Methods
Different subtypes of fibrous epulides and normal gingival tissue specimens were first collected for histological and immunofluorescence analyses to see if fibrocytes were present and whether they differentiated into myofibroblasts and osteoblasts upon stimulated by transforming growth factor‐β1 (TGF‐β1). Electron microscopy and elemental analysis were used to characterize the extracellular microenvironment in different subtypes of fibrous epulides. Human peripheral blood mononuclear cells (PBMCs) were subsequently isolated from in vitro models to mimic the microenvironment in fibrous epulides to identify whether TGF‐β1 as well as the calcium and phosphorus ion concentration in the extracellular matrix (ECM) of a fibrous epulis trigger fibrocyte differentiation.
Results
Fibrous epulides contain fibrocytes that accumulate in the local inflammatory environment and have the ability to differentiate into myofibroblasts or osteoblasts. TGF‐β1 promotes fibrocytes differentiation into myofibroblasts in a concentration‐dependent manner, while TGF‐β1 stimulates the fibrocytes to differentiate into osteoblasts when combined with a high calcium and phosphorus environment.
Conclusions
Our study revealed fibrocytes play an important role in the fibrogenesis and osteogenesis in fibrous epulis, and might serve as a therapeutic target for the inhibition of recurrence of fibrous epulides. |
doi_str_mv | 10.1111/odi.14847 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2906773144</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3113654301</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3137-97e49c47e1d5f87cba66a88b059fedb092aaaeec31184a48d9443edf8c89732f3</originalsourceid><addsrcrecordid>eNp1kEFLwzAUx4Mobk4PfgEJeNFDt6RJm8STYzodDHZR8BbS9nXL6NrarMi-vdk6PQi-y3uH3_vx54_QNSVD6mdUZXZIueTiBPVpTGhAZBid-ptFPIhC9tFDF86tCaFCsfAc9Zg84KqPHqc2aap0t4UHPMYb65wtl7i2kAK2Jd6uANdmu6qWUIKzDlc5zvcfrcNQt4V1l-gsN4WDq-MeoPfp89vkNZgvXmaT8TxIGWUiUAK4SrkAmkW5FGli4thImZBI5ZAlRIXGGAAPU8kNl5ninEGWy1QqwcKcDdBd562b6rMFt9U-bApFYUrwaXSoSCwEo_5tgG7_oOuqbUqfTns9iyPOCPXUfUelTeVcA7muG7sxzU5Tove1al-rPvTk2ZujsU02kP2SPz16YNQBX7aA3f8mvXiadcpvIpiAIQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3113654301</pqid></control><display><type>article</type><title>Fibrocyte: A missing piece in the pathogenesis of fibrous epulis</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Zhu, Yi‐fei ; Wan, Mei‐chen ; Gao, Peng ; Shen, Min‐juan ; Zhu, Yi‐na ; Hao, Jia‐xin ; Lu, Wei‐cheng ; Wang, Chen‐yu ; Tay, Franklin ; Ehrlich, Hermann ; Niu, Li‐na ; Jiao, Kai</creator><creatorcontrib>Zhu, Yi‐fei ; Wan, Mei‐chen ; Gao, Peng ; Shen, Min‐juan ; Zhu, Yi‐na ; Hao, Jia‐xin ; Lu, Wei‐cheng ; Wang, Chen‐yu ; Tay, Franklin ; Ehrlich, Hermann ; Niu, Li‐na ; Jiao, Kai</creatorcontrib><description>Objectives
To explore the role of fibrocytes in the recurrence and calcification of fibrous epulides.
Methods
Different subtypes of fibrous epulides and normal gingival tissue specimens were first collected for histological and immunofluorescence analyses to see if fibrocytes were present and whether they differentiated into myofibroblasts and osteoblasts upon stimulated by transforming growth factor‐β1 (TGF‐β1). Electron microscopy and elemental analysis were used to characterize the extracellular microenvironment in different subtypes of fibrous epulides. Human peripheral blood mononuclear cells (PBMCs) were subsequently isolated from in vitro models to mimic the microenvironment in fibrous epulides to identify whether TGF‐β1 as well as the calcium and phosphorus ion concentration in the extracellular matrix (ECM) of a fibrous epulis trigger fibrocyte differentiation.
Results
Fibrous epulides contain fibrocytes that accumulate in the local inflammatory environment and have the ability to differentiate into myofibroblasts or osteoblasts. TGF‐β1 promotes fibrocytes differentiation into myofibroblasts in a concentration‐dependent manner, while TGF‐β1 stimulates the fibrocytes to differentiate into osteoblasts when combined with a high calcium and phosphorus environment.
Conclusions
Our study revealed fibrocytes play an important role in the fibrogenesis and osteogenesis in fibrous epulis, and might serve as a therapeutic target for the inhibition of recurrence of fibrous epulides.</description><identifier>ISSN: 1354-523X</identifier><identifier>ISSN: 1601-0825</identifier><identifier>EISSN: 1601-0825</identifier><identifier>DOI: 10.1111/odi.14847</identifier><identifier>PMID: 38148479</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>Calcification ; Calcium (extracellular) ; Calcium - metabolism ; Cell culture ; Cell Differentiation ; Cells, Cultured ; Electron microscopy ; Extracellular matrix ; Extracellular Matrix - metabolism ; Extracellular Matrix - pathology ; Fibroblasts - pathology ; fibrocyte ; fibrous epulis ; Gingiva - cytology ; Gingiva - pathology ; Gingival Diseases - pathology ; Humans ; Immunofluorescence ; Leukocytes (mononuclear) ; Leukocytes, Mononuclear - pathology ; Microenvironments ; myofibroblast ; Myofibroblasts - pathology ; osteoblast ; Osteoblastogenesis ; Osteoblasts ; Osteoblasts - pathology ; Osteogenesis ; Peripheral blood mononuclear cells ; Phosphorus ; Phosphorus - analysis ; TGF‐β1 ; Therapeutic targets ; Transforming Growth Factor beta1 - metabolism ; Transforming Growth Factor beta1 - pharmacology</subject><ispartof>Oral diseases, 2024-10, Vol.30 (7), p.4376-4389</ispartof><rights>2023 Wiley Periodicals LLC.</rights><rights>2024 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3137-97e49c47e1d5f87cba66a88b059fedb092aaaeec31184a48d9443edf8c89732f3</cites><orcidid>0000-0002-6653-0819</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fodi.14847$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fodi.14847$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27926,27927,45576,45577</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38148479$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Yi‐fei</creatorcontrib><creatorcontrib>Wan, Mei‐chen</creatorcontrib><creatorcontrib>Gao, Peng</creatorcontrib><creatorcontrib>Shen, Min‐juan</creatorcontrib><creatorcontrib>Zhu, Yi‐na</creatorcontrib><creatorcontrib>Hao, Jia‐xin</creatorcontrib><creatorcontrib>Lu, Wei‐cheng</creatorcontrib><creatorcontrib>Wang, Chen‐yu</creatorcontrib><creatorcontrib>Tay, Franklin</creatorcontrib><creatorcontrib>Ehrlich, Hermann</creatorcontrib><creatorcontrib>Niu, Li‐na</creatorcontrib><creatorcontrib>Jiao, Kai</creatorcontrib><title>Fibrocyte: A missing piece in the pathogenesis of fibrous epulis</title><title>Oral diseases</title><addtitle>Oral Dis</addtitle><description>Objectives
To explore the role of fibrocytes in the recurrence and calcification of fibrous epulides.
Methods
Different subtypes of fibrous epulides and normal gingival tissue specimens were first collected for histological and immunofluorescence analyses to see if fibrocytes were present and whether they differentiated into myofibroblasts and osteoblasts upon stimulated by transforming growth factor‐β1 (TGF‐β1). Electron microscopy and elemental analysis were used to characterize the extracellular microenvironment in different subtypes of fibrous epulides. Human peripheral blood mononuclear cells (PBMCs) were subsequently isolated from in vitro models to mimic the microenvironment in fibrous epulides to identify whether TGF‐β1 as well as the calcium and phosphorus ion concentration in the extracellular matrix (ECM) of a fibrous epulis trigger fibrocyte differentiation.
Results
Fibrous epulides contain fibrocytes that accumulate in the local inflammatory environment and have the ability to differentiate into myofibroblasts or osteoblasts. TGF‐β1 promotes fibrocytes differentiation into myofibroblasts in a concentration‐dependent manner, while TGF‐β1 stimulates the fibrocytes to differentiate into osteoblasts when combined with a high calcium and phosphorus environment.
Conclusions
Our study revealed fibrocytes play an important role in the fibrogenesis and osteogenesis in fibrous epulis, and might serve as a therapeutic target for the inhibition of recurrence of fibrous epulides.</description><subject>Calcification</subject><subject>Calcium (extracellular)</subject><subject>Calcium - metabolism</subject><subject>Cell culture</subject><subject>Cell Differentiation</subject><subject>Cells, Cultured</subject><subject>Electron microscopy</subject><subject>Extracellular matrix</subject><subject>Extracellular Matrix - metabolism</subject><subject>Extracellular Matrix - pathology</subject><subject>Fibroblasts - pathology</subject><subject>fibrocyte</subject><subject>fibrous epulis</subject><subject>Gingiva - cytology</subject><subject>Gingiva - pathology</subject><subject>Gingival Diseases - pathology</subject><subject>Humans</subject><subject>Immunofluorescence</subject><subject>Leukocytes (mononuclear)</subject><subject>Leukocytes, Mononuclear - pathology</subject><subject>Microenvironments</subject><subject>myofibroblast</subject><subject>Myofibroblasts - pathology</subject><subject>osteoblast</subject><subject>Osteoblastogenesis</subject><subject>Osteoblasts</subject><subject>Osteoblasts - pathology</subject><subject>Osteogenesis</subject><subject>Peripheral blood mononuclear cells</subject><subject>Phosphorus</subject><subject>Phosphorus - analysis</subject><subject>TGF‐β1</subject><subject>Therapeutic targets</subject><subject>Transforming Growth Factor beta1 - metabolism</subject><subject>Transforming Growth Factor beta1 - pharmacology</subject><issn>1354-523X</issn><issn>1601-0825</issn><issn>1601-0825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEFLwzAUx4Mobk4PfgEJeNFDt6RJm8STYzodDHZR8BbS9nXL6NrarMi-vdk6PQi-y3uH3_vx54_QNSVD6mdUZXZIueTiBPVpTGhAZBid-ptFPIhC9tFDF86tCaFCsfAc9Zg84KqPHqc2aap0t4UHPMYb65wtl7i2kAK2Jd6uANdmu6qWUIKzDlc5zvcfrcNQt4V1l-gsN4WDq-MeoPfp89vkNZgvXmaT8TxIGWUiUAK4SrkAmkW5FGli4thImZBI5ZAlRIXGGAAPU8kNl5ninEGWy1QqwcKcDdBd562b6rMFt9U-bApFYUrwaXSoSCwEo_5tgG7_oOuqbUqfTns9iyPOCPXUfUelTeVcA7muG7sxzU5Tove1al-rPvTk2ZujsU02kP2SPz16YNQBX7aA3f8mvXiadcpvIpiAIQ</recordid><startdate>202410</startdate><enddate>202410</enddate><creator>Zhu, Yi‐fei</creator><creator>Wan, Mei‐chen</creator><creator>Gao, Peng</creator><creator>Shen, Min‐juan</creator><creator>Zhu, Yi‐na</creator><creator>Hao, Jia‐xin</creator><creator>Lu, Wei‐cheng</creator><creator>Wang, Chen‐yu</creator><creator>Tay, Franklin</creator><creator>Ehrlich, Hermann</creator><creator>Niu, Li‐na</creator><creator>Jiao, Kai</creator><general>Wiley Subscription Services, Inc</general><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/0000-0002-6653-0819</orcidid></search><sort><creationdate>202410</creationdate><title>Fibrocyte: A missing piece in the pathogenesis of fibrous epulis</title><author>Zhu, Yi‐fei ; Wan, Mei‐chen ; Gao, Peng ; Shen, Min‐juan ; Zhu, Yi‐na ; Hao, Jia‐xin ; Lu, Wei‐cheng ; Wang, Chen‐yu ; Tay, Franklin ; Ehrlich, Hermann ; Niu, Li‐na ; Jiao, Kai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3137-97e49c47e1d5f87cba66a88b059fedb092aaaeec31184a48d9443edf8c89732f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Calcification</topic><topic>Calcium (extracellular)</topic><topic>Calcium - metabolism</topic><topic>Cell culture</topic><topic>Cell Differentiation</topic><topic>Cells, Cultured</topic><topic>Electron microscopy</topic><topic>Extracellular matrix</topic><topic>Extracellular Matrix - metabolism</topic><topic>Extracellular Matrix - pathology</topic><topic>Fibroblasts - pathology</topic><topic>fibrocyte</topic><topic>fibrous epulis</topic><topic>Gingiva - cytology</topic><topic>Gingiva - pathology</topic><topic>Gingival Diseases - pathology</topic><topic>Humans</topic><topic>Immunofluorescence</topic><topic>Leukocytes (mononuclear)</topic><topic>Leukocytes, Mononuclear - pathology</topic><topic>Microenvironments</topic><topic>myofibroblast</topic><topic>Myofibroblasts - pathology</topic><topic>osteoblast</topic><topic>Osteoblastogenesis</topic><topic>Osteoblasts</topic><topic>Osteoblasts - pathology</topic><topic>Osteogenesis</topic><topic>Peripheral blood mononuclear cells</topic><topic>Phosphorus</topic><topic>Phosphorus - analysis</topic><topic>TGF‐β1</topic><topic>Therapeutic targets</topic><topic>Transforming Growth Factor beta1 - metabolism</topic><topic>Transforming Growth Factor beta1 - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Yi‐fei</creatorcontrib><creatorcontrib>Wan, Mei‐chen</creatorcontrib><creatorcontrib>Gao, Peng</creatorcontrib><creatorcontrib>Shen, Min‐juan</creatorcontrib><creatorcontrib>Zhu, Yi‐na</creatorcontrib><creatorcontrib>Hao, Jia‐xin</creatorcontrib><creatorcontrib>Lu, Wei‐cheng</creatorcontrib><creatorcontrib>Wang, Chen‐yu</creatorcontrib><creatorcontrib>Tay, Franklin</creatorcontrib><creatorcontrib>Ehrlich, Hermann</creatorcontrib><creatorcontrib>Niu, Li‐na</creatorcontrib><creatorcontrib>Jiao, Kai</creatorcontrib><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>Zhu, Yi‐fei</au><au>Wan, Mei‐chen</au><au>Gao, Peng</au><au>Shen, Min‐juan</au><au>Zhu, Yi‐na</au><au>Hao, Jia‐xin</au><au>Lu, Wei‐cheng</au><au>Wang, Chen‐yu</au><au>Tay, Franklin</au><au>Ehrlich, Hermann</au><au>Niu, Li‐na</au><au>Jiao, Kai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fibrocyte: A missing piece in the pathogenesis of fibrous epulis</atitle><jtitle>Oral diseases</jtitle><addtitle>Oral Dis</addtitle><date>2024-10</date><risdate>2024</risdate><volume>30</volume><issue>7</issue><spage>4376</spage><epage>4389</epage><pages>4376-4389</pages><issn>1354-523X</issn><issn>1601-0825</issn><eissn>1601-0825</eissn><abstract>Objectives
To explore the role of fibrocytes in the recurrence and calcification of fibrous epulides.
Methods
Different subtypes of fibrous epulides and normal gingival tissue specimens were first collected for histological and immunofluorescence analyses to see if fibrocytes were present and whether they differentiated into myofibroblasts and osteoblasts upon stimulated by transforming growth factor‐β1 (TGF‐β1). Electron microscopy and elemental analysis were used to characterize the extracellular microenvironment in different subtypes of fibrous epulides. Human peripheral blood mononuclear cells (PBMCs) were subsequently isolated from in vitro models to mimic the microenvironment in fibrous epulides to identify whether TGF‐β1 as well as the calcium and phosphorus ion concentration in the extracellular matrix (ECM) of a fibrous epulis trigger fibrocyte differentiation.
Results
Fibrous epulides contain fibrocytes that accumulate in the local inflammatory environment and have the ability to differentiate into myofibroblasts or osteoblasts. TGF‐β1 promotes fibrocytes differentiation into myofibroblasts in a concentration‐dependent manner, while TGF‐β1 stimulates the fibrocytes to differentiate into osteoblasts when combined with a high calcium and phosphorus environment.
Conclusions
Our study revealed fibrocytes play an important role in the fibrogenesis and osteogenesis in fibrous epulis, and might serve as a therapeutic target for the inhibition of recurrence of fibrous epulides.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38148479</pmid><doi>10.1111/odi.14847</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-6653-0819</orcidid></addata></record> |
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subjects | Calcification Calcium (extracellular) Calcium - metabolism Cell culture Cell Differentiation Cells, Cultured Electron microscopy Extracellular matrix Extracellular Matrix - metabolism Extracellular Matrix - pathology Fibroblasts - pathology fibrocyte fibrous epulis Gingiva - cytology Gingiva - pathology Gingival Diseases - pathology Humans Immunofluorescence Leukocytes (mononuclear) Leukocytes, Mononuclear - pathology Microenvironments myofibroblast Myofibroblasts - pathology osteoblast Osteoblastogenesis Osteoblasts Osteoblasts - pathology Osteogenesis Peripheral blood mononuclear cells Phosphorus Phosphorus - analysis TGF‐β1 Therapeutic targets Transforming Growth Factor beta1 - metabolism Transforming Growth Factor beta1 - pharmacology |
title | Fibrocyte: A missing piece in the pathogenesis of fibrous epulis |
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