Schwann cells secrete extracellular vesicles to promote and maintain the proliferation and multipotency of hDPCs
Objectives Schwann cells (SCs) are the principal glial cells in peripheral nerve system, involved in neuropathies with great regenerative potential. Dental pulp cells have been reported to maintain neurogenic potential. In contrast, the regulatory role of SCs on human dental pulp cells (hDPCs) devel...
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creator | Li, Ziyue Liang, Yan Pan, Kuangwu Li, Hui Yu, Mei Guo, Weihua Chen, Guoqing Tian, Weidong |
description | Objectives
Schwann cells (SCs) are the principal glial cells in peripheral nerve system, involved in neuropathies with great regenerative potential. Dental pulp cells have been reported to maintain neurogenic potential. In contrast, the regulatory role of SCs on human dental pulp cells (hDPCs) development remains undefined.
Materials and methods
SC secretion and SC‐derived extracellular vesicles (EVs) were collected and used to treat hDPCs; and proliferation and multiple differentiation of hDPCs were detected after EVs treatments. Finally, we analysed the proteomes of SC‐EVs and SCs through mass spectrum.
Results
In this study, we found SC secretion showed a predominantly regulatory role on the development of hDPCs. Further, we identified EVs from SC secretion with similar function as SC secretion in regulating hDPCs proliferation and multipotency. And expression of transcription factor Oct4 was upregulated after treatment of both SC secretion and EVs, as well as Sox2 and Nanog. We detected abundant enrichment of Oct4 in EVs, which might be responsible for the upregulation of stem cell‐related genes in hDPCs. Through proteome and western blot analysis, we found enriched TGFβs in EVs, indicating that accelerated hDPCs proliferation may be mediated by activated TGFβ‐Samd and TGFβ‐MAPK signalling.
Conclusions
In summary, our study sheds light on critical regulatory ability of SC‐derived EVs on hDPCs proliferation and multipotency, suggesting great implications for seeding cells used in tissue engineering. |
doi_str_mv | 10.1111/cpr.12353 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6529079</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1920464013</sourcerecordid><originalsourceid>FETCH-LOGICAL-p3693-1fa1b49ec860366f735f97323bf031148a36a65aeede33adcf50bf1a4754d8c53</originalsourceid><addsrcrecordid>eNpdkV1rFDEUhoModq1e-Ack4I030yaTr5kbQVarQsHix3XIZk7clEwyJjOt---b3a1FDYQc8j68nHNehF5SckbrObdTPqMtE-wRWlEmRdPSjj9GK9JL0ijVtifoWSnXhFBGlXyKTtpOUU6VWKHpm93emhixhRAKLmAzzIDh95zN_msJJuMbKN4GKHhOeMppTJUwccCj8XGuF89b2AvBO8hm9ike5SXMfqpwtDucHN6-v1qX5-iJM6HAi_v3FP24-PB9_am5_PLx8_rdZTMx2bOGOkM3vAfbScKkdIoJ1yvWso0jjFLeGSaNFAZgAMbMYJ0gG0cNV4IPnRXsFL09-k7LZoTBQqwTBT1lP5q808l4_a8S_Vb_TDdairYnqq8Gb-4Ncvq1QJn16Mt-JSZCWoqmfUto33FOKvr6P_Q6LTnW8Q4Ul7xuvlKv_u7ooZU_YVTg_Ajc-gC7B50SvU9Z15T1IWW9vvp6KNgdGkycCQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1920464013</pqid></control><display><type>article</type><title>Schwann cells secrete extracellular vesicles to promote and maintain the proliferation and multipotency of hDPCs</title><source>Wiley Online Library - AutoHoldings Journals</source><source>MEDLINE</source><source>PubMed Central (PMC)</source><creator>Li, Ziyue ; Liang, Yan ; Pan, Kuangwu ; Li, Hui ; Yu, Mei ; Guo, Weihua ; Chen, Guoqing ; Tian, Weidong</creator><creatorcontrib>Li, Ziyue ; Liang, Yan ; Pan, Kuangwu ; Li, Hui ; Yu, Mei ; Guo, Weihua ; Chen, Guoqing ; Tian, Weidong</creatorcontrib><description>Objectives
Schwann cells (SCs) are the principal glial cells in peripheral nerve system, involved in neuropathies with great regenerative potential. Dental pulp cells have been reported to maintain neurogenic potential. In contrast, the regulatory role of SCs on human dental pulp cells (hDPCs) development remains undefined.
Materials and methods
SC secretion and SC‐derived extracellular vesicles (EVs) were collected and used to treat hDPCs; and proliferation and multiple differentiation of hDPCs were detected after EVs treatments. Finally, we analysed the proteomes of SC‐EVs and SCs through mass spectrum.
Results
In this study, we found SC secretion showed a predominantly regulatory role on the development of hDPCs. Further, we identified EVs from SC secretion with similar function as SC secretion in regulating hDPCs proliferation and multipotency. And expression of transcription factor Oct4 was upregulated after treatment of both SC secretion and EVs, as well as Sox2 and Nanog. We detected abundant enrichment of Oct4 in EVs, which might be responsible for the upregulation of stem cell‐related genes in hDPCs. Through proteome and western blot analysis, we found enriched TGFβs in EVs, indicating that accelerated hDPCs proliferation may be mediated by activated TGFβ‐Samd and TGFβ‐MAPK signalling.
Conclusions
In summary, our study sheds light on critical regulatory ability of SC‐derived EVs on hDPCs proliferation and multipotency, suggesting great implications for seeding cells used in tissue engineering.</description><identifier>ISSN: 0960-7722</identifier><identifier>EISSN: 1365-2184</identifier><identifier>DOI: 10.1111/cpr.12353</identifier><identifier>PMID: 28714175</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Cell Differentiation ; Cell Proliferation ; Cells, Cultured ; Chromatography, High Pressure Liquid ; Dental materials ; Dental pulp ; Dental Pulp - cytology ; Differentiation ; Extracellular vesicles ; Extracellular Vesicles - metabolism ; Glial cells ; Humans ; MAP kinase ; Microscopy, Fluorescence ; Nanog Homeobox Protein - genetics ; Nanog Homeobox Protein - metabolism ; Neuronal-glial interactions ; Oct-4 protein ; Octamer Transcription Factor-3 - genetics ; Octamer Transcription Factor-3 - metabolism ; Original ; Peripheral neuropathy ; Proteome - analysis ; Proteomes ; Schwann cells ; Schwann Cells - cytology ; Schwann Cells - metabolism ; Secretion ; Signal Transduction - drug effects ; Signaling ; Smad Proteins - metabolism ; SOXB1 Transcription Factors - genetics ; SOXB1 Transcription Factors - metabolism ; Stem cells ; Stem Cells - cytology ; Stem Cells - metabolism ; Tandem Mass Spectrometry ; Tissue engineering ; Transforming Growth Factor beta - metabolism ; Up-Regulation ; Vesicles</subject><ispartof>Cell proliferation, 2017-08, Vol.50 (4), p.n/a</ispartof><rights>2017 John Wiley & Sons Ltd</rights><rights>2017 John Wiley & Sons Ltd.</rights><rights>Copyright © 2017 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0003-0175-1132 ; 0000-0003-0306-6817</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/PMC6529079/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529079/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1416,27922,27923,45572,45573,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28714175$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Ziyue</creatorcontrib><creatorcontrib>Liang, Yan</creatorcontrib><creatorcontrib>Pan, Kuangwu</creatorcontrib><creatorcontrib>Li, Hui</creatorcontrib><creatorcontrib>Yu, Mei</creatorcontrib><creatorcontrib>Guo, Weihua</creatorcontrib><creatorcontrib>Chen, Guoqing</creatorcontrib><creatorcontrib>Tian, Weidong</creatorcontrib><title>Schwann cells secrete extracellular vesicles to promote and maintain the proliferation and multipotency of hDPCs</title><title>Cell proliferation</title><addtitle>Cell Prolif</addtitle><description>Objectives
Schwann cells (SCs) are the principal glial cells in peripheral nerve system, involved in neuropathies with great regenerative potential. Dental pulp cells have been reported to maintain neurogenic potential. In contrast, the regulatory role of SCs on human dental pulp cells (hDPCs) development remains undefined.
Materials and methods
SC secretion and SC‐derived extracellular vesicles (EVs) were collected and used to treat hDPCs; and proliferation and multiple differentiation of hDPCs were detected after EVs treatments. Finally, we analysed the proteomes of SC‐EVs and SCs through mass spectrum.
Results
In this study, we found SC secretion showed a predominantly regulatory role on the development of hDPCs. Further, we identified EVs from SC secretion with similar function as SC secretion in regulating hDPCs proliferation and multipotency. And expression of transcription factor Oct4 was upregulated after treatment of both SC secretion and EVs, as well as Sox2 and Nanog. We detected abundant enrichment of Oct4 in EVs, which might be responsible for the upregulation of stem cell‐related genes in hDPCs. Through proteome and western blot analysis, we found enriched TGFβs in EVs, indicating that accelerated hDPCs proliferation may be mediated by activated TGFβ‐Samd and TGFβ‐MAPK signalling.
Conclusions
In summary, our study sheds light on critical regulatory ability of SC‐derived EVs on hDPCs proliferation and multipotency, suggesting great implications for seeding cells used in tissue engineering.</description><subject>Cell Differentiation</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Dental materials</subject><subject>Dental pulp</subject><subject>Dental Pulp - cytology</subject><subject>Differentiation</subject><subject>Extracellular vesicles</subject><subject>Extracellular Vesicles - metabolism</subject><subject>Glial cells</subject><subject>Humans</subject><subject>MAP kinase</subject><subject>Microscopy, Fluorescence</subject><subject>Nanog Homeobox Protein - genetics</subject><subject>Nanog Homeobox Protein - metabolism</subject><subject>Neuronal-glial interactions</subject><subject>Oct-4 protein</subject><subject>Octamer Transcription Factor-3 - genetics</subject><subject>Octamer Transcription Factor-3 - metabolism</subject><subject>Original</subject><subject>Peripheral neuropathy</subject><subject>Proteome - analysis</subject><subject>Proteomes</subject><subject>Schwann cells</subject><subject>Schwann Cells - cytology</subject><subject>Schwann Cells - metabolism</subject><subject>Secretion</subject><subject>Signal Transduction - drug effects</subject><subject>Signaling</subject><subject>Smad Proteins - metabolism</subject><subject>SOXB1 Transcription Factors - genetics</subject><subject>SOXB1 Transcription Factors - metabolism</subject><subject>Stem cells</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - metabolism</subject><subject>Tandem Mass Spectrometry</subject><subject>Tissue engineering</subject><subject>Transforming Growth Factor beta - metabolism</subject><subject>Up-Regulation</subject><subject>Vesicles</subject><issn>0960-7722</issn><issn>1365-2184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkV1rFDEUhoModq1e-Ack4I030yaTr5kbQVarQsHix3XIZk7clEwyJjOt---b3a1FDYQc8j68nHNehF5SckbrObdTPqMtE-wRWlEmRdPSjj9GK9JL0ijVtifoWSnXhFBGlXyKTtpOUU6VWKHpm93emhixhRAKLmAzzIDh95zN_msJJuMbKN4GKHhOeMppTJUwccCj8XGuF89b2AvBO8hm9ike5SXMfqpwtDucHN6-v1qX5-iJM6HAi_v3FP24-PB9_am5_PLx8_rdZTMx2bOGOkM3vAfbScKkdIoJ1yvWso0jjFLeGSaNFAZgAMbMYJ0gG0cNV4IPnRXsFL09-k7LZoTBQqwTBT1lP5q808l4_a8S_Vb_TDdairYnqq8Gb-4Ncvq1QJn16Mt-JSZCWoqmfUto33FOKvr6P_Q6LTnW8Q4Ul7xuvlKv_u7ooZU_YVTg_Ajc-gC7B50SvU9Z15T1IWW9vvp6KNgdGkycCQ</recordid><startdate>201708</startdate><enddate>201708</enddate><creator>Li, Ziyue</creator><creator>Liang, Yan</creator><creator>Pan, Kuangwu</creator><creator>Li, Hui</creator><creator>Yu, Mei</creator><creator>Guo, Weihua</creator><creator>Chen, Guoqing</creator><creator>Tian, Weidong</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0175-1132</orcidid><orcidid>https://orcid.org/0000-0003-0306-6817</orcidid></search><sort><creationdate>201708</creationdate><title>Schwann cells secrete extracellular vesicles to promote and maintain the proliferation and multipotency of hDPCs</title><author>Li, Ziyue ; Liang, Yan ; Pan, Kuangwu ; Li, Hui ; Yu, Mei ; Guo, Weihua ; Chen, Guoqing ; Tian, Weidong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p3693-1fa1b49ec860366f735f97323bf031148a36a65aeede33adcf50bf1a4754d8c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Cell Differentiation</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Dental materials</topic><topic>Dental pulp</topic><topic>Dental Pulp - cytology</topic><topic>Differentiation</topic><topic>Extracellular vesicles</topic><topic>Extracellular Vesicles - metabolism</topic><topic>Glial cells</topic><topic>Humans</topic><topic>MAP kinase</topic><topic>Microscopy, Fluorescence</topic><topic>Nanog Homeobox Protein - genetics</topic><topic>Nanog Homeobox Protein - metabolism</topic><topic>Neuronal-glial interactions</topic><topic>Oct-4 protein</topic><topic>Octamer Transcription Factor-3 - genetics</topic><topic>Octamer Transcription Factor-3 - metabolism</topic><topic>Original</topic><topic>Peripheral neuropathy</topic><topic>Proteome - analysis</topic><topic>Proteomes</topic><topic>Schwann cells</topic><topic>Schwann Cells - cytology</topic><topic>Schwann Cells - metabolism</topic><topic>Secretion</topic><topic>Signal Transduction - drug effects</topic><topic>Signaling</topic><topic>Smad Proteins - metabolism</topic><topic>SOXB1 Transcription Factors - genetics</topic><topic>SOXB1 Transcription Factors - metabolism</topic><topic>Stem cells</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - metabolism</topic><topic>Tandem Mass Spectrometry</topic><topic>Tissue engineering</topic><topic>Transforming Growth Factor beta - metabolism</topic><topic>Up-Regulation</topic><topic>Vesicles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Ziyue</creatorcontrib><creatorcontrib>Liang, Yan</creatorcontrib><creatorcontrib>Pan, Kuangwu</creatorcontrib><creatorcontrib>Li, Hui</creatorcontrib><creatorcontrib>Yu, Mei</creatorcontrib><creatorcontrib>Guo, Weihua</creatorcontrib><creatorcontrib>Chen, Guoqing</creatorcontrib><creatorcontrib>Tian, Weidong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell proliferation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Ziyue</au><au>Liang, Yan</au><au>Pan, Kuangwu</au><au>Li, Hui</au><au>Yu, Mei</au><au>Guo, Weihua</au><au>Chen, Guoqing</au><au>Tian, Weidong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Schwann cells secrete extracellular vesicles to promote and maintain the proliferation and multipotency of hDPCs</atitle><jtitle>Cell proliferation</jtitle><addtitle>Cell Prolif</addtitle><date>2017-08</date><risdate>2017</risdate><volume>50</volume><issue>4</issue><epage>n/a</epage><issn>0960-7722</issn><eissn>1365-2184</eissn><abstract>Objectives
Schwann cells (SCs) are the principal glial cells in peripheral nerve system, involved in neuropathies with great regenerative potential. Dental pulp cells have been reported to maintain neurogenic potential. In contrast, the regulatory role of SCs on human dental pulp cells (hDPCs) development remains undefined.
Materials and methods
SC secretion and SC‐derived extracellular vesicles (EVs) were collected and used to treat hDPCs; and proliferation and multiple differentiation of hDPCs were detected after EVs treatments. Finally, we analysed the proteomes of SC‐EVs and SCs through mass spectrum.
Results
In this study, we found SC secretion showed a predominantly regulatory role on the development of hDPCs. Further, we identified EVs from SC secretion with similar function as SC secretion in regulating hDPCs proliferation and multipotency. And expression of transcription factor Oct4 was upregulated after treatment of both SC secretion and EVs, as well as Sox2 and Nanog. We detected abundant enrichment of Oct4 in EVs, which might be responsible for the upregulation of stem cell‐related genes in hDPCs. Through proteome and western blot analysis, we found enriched TGFβs in EVs, indicating that accelerated hDPCs proliferation may be mediated by activated TGFβ‐Samd and TGFβ‐MAPK signalling.
Conclusions
In summary, our study sheds light on critical regulatory ability of SC‐derived EVs on hDPCs proliferation and multipotency, suggesting great implications for seeding cells used in tissue engineering.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>28714175</pmid><doi>10.1111/cpr.12353</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-0175-1132</orcidid><orcidid>https://orcid.org/0000-0003-0306-6817</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Cell Differentiation Cell Proliferation Cells, Cultured Chromatography, High Pressure Liquid Dental materials Dental pulp Dental Pulp - cytology Differentiation Extracellular vesicles Extracellular Vesicles - metabolism Glial cells Humans MAP kinase Microscopy, Fluorescence Nanog Homeobox Protein - genetics Nanog Homeobox Protein - metabolism Neuronal-glial interactions Oct-4 protein Octamer Transcription Factor-3 - genetics Octamer Transcription Factor-3 - metabolism Original Peripheral neuropathy Proteome - analysis Proteomes Schwann cells Schwann Cells - cytology Schwann Cells - metabolism Secretion Signal Transduction - drug effects Signaling Smad Proteins - metabolism SOXB1 Transcription Factors - genetics SOXB1 Transcription Factors - metabolism Stem cells Stem Cells - cytology Stem Cells - metabolism Tandem Mass Spectrometry Tissue engineering Transforming Growth Factor beta - metabolism Up-Regulation Vesicles |
title | Schwann cells secrete extracellular vesicles to promote and maintain the proliferation and multipotency of hDPCs |
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