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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Veröffentlicht in:Cell proliferation 2017-08, Vol.50 (4), p.n/a
Hauptverfasser: Li, Ziyue, Liang, Yan, Pan, Kuangwu, Li, Hui, Yu, Mei, Guo, Weihua, Chen, Guoqing, Tian, Weidong
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container_issue 4
container_start_page
container_title Cell proliferation
container_volume 50
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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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 &amp; 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 &amp; Sons Ltd</rights><rights>2017 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2017 John Wiley &amp; 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 &amp; 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 &amp; 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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source Wiley Online Library - AutoHoldings Journals; MEDLINE; PubMed Central (PMC)
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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