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Response to light compressive force in human cementoblasts in vitro
The objective of this study is to investigate the responses of human cementoblasts to light compressive force in vitro. A human cementoblast cell line (HCEM) was loaded for 12 h by mounting coverslips (0.25 gf/cm2). The coverslips were removed and the cells were cultured for up to 21 days. Cells wit...
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Published in: | Biomedical Research 2016/10/01, Vol.37(5), pp.293-298 |
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description | The objective of this study is to investigate the responses of human cementoblasts to light compressive force in vitro. A human cementoblast cell line (HCEM) was loaded for 12 h by mounting coverslips (0.25 gf/cm2). The coverslips were removed and the cells were cultured for up to 21 days. Cells without glass loading were used as controls. Cell growth, morphological changes, and the mRNA expression of RUNX2, ALP, WNT5A and SPON1 were investigated. No significant differences were observed in cell numbers between the compressed group and control group. Morphology of the compressed cells was slightly flattened on day 0; however, no indications of cell death were detected. Expression of differentiation markers including RUNX2, ALP and WNT5A was significantly lower in the compressed group (0.7, 0.75 and 0.75-fold respectively, P < 0.05) than in the control group on day 7. The expression levels of SPON1, a differentiation marker of cementoblasts, were higher on days 7 and 14 than on day 0, but were lower in the compressed group than in the control group (P < 0.01). These results suggest that light compressive force does not affect cell growth and morphology, but restrains higher expression of cementogenic differentiation markers in human cementoblasts in vitro. |
doi_str_mv | 10.2220/biomedres.37.293 |
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A human cementoblast cell line (HCEM) was loaded for 12 h by mounting coverslips (0.25 gf/cm2). The coverslips were removed and the cells were cultured for up to 21 days. Cells without glass loading were used as controls. Cell growth, morphological changes, and the mRNA expression of RUNX2, ALP, WNT5A and SPON1 were investigated. No significant differences were observed in cell numbers between the compressed group and control group. Morphology of the compressed cells was slightly flattened on day 0; however, no indications of cell death were detected. Expression of differentiation markers including RUNX2, ALP and WNT5A was significantly lower in the compressed group (0.7, 0.75 and 0.75-fold respectively, P < 0.05) than in the control group on day 7. The expression levels of SPON1, a differentiation marker of cementoblasts, were higher on days 7 and 14 than on day 0, but were lower in the compressed group than in the control group (P < 0.01). These results suggest that light compressive force does not affect cell growth and morphology, but restrains higher expression of cementogenic differentiation markers in human cementoblasts in vitro.</description><identifier>ISSN: 0388-6107</identifier><identifier>EISSN: 1880-313X</identifier><identifier>DOI: 10.2220/biomedres.37.293</identifier><identifier>PMID: 27784872</identifier><language>eng</language><publisher>Japan: Biomedical Research Press</publisher><subject>Biomarkers ; Cbfa-1 protein ; Cell death ; Cell differentiation ; Cell growth ; Cell Line ; Cell morphology ; Cementogenesis - genetics ; Compressive Strength ; Cytology ; Dental Cementum - metabolism ; Differentiation ; Gene expression ; Gene Expression Regulation ; Humans ; In Vitro Techniques ; Morphology ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Studies ; Wnt protein</subject><ispartof>Biomedical Research, 2016/10/01, Vol.37(5), pp.293-298</ispartof><rights>2016 Biomedical Research Press</rights><rights>Copyright Japan Science and Technology Agency 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c620t-b9ac0205b260199ff9feac95f67aef41e1987874b3c07230b8b03cfc3551a40e3</citedby><cites>FETCH-LOGICAL-c620t-b9ac0205b260199ff9feac95f67aef41e1987874b3c07230b8b03cfc3551a40e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1882,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27784872$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MATSUNAGA, Kenji</creatorcontrib><creatorcontrib>ITO, Chika</creatorcontrib><creatorcontrib>NAKAKOGAWA, Kaichi</creatorcontrib><creatorcontrib>SUGIUCHI, Akina</creatorcontrib><creatorcontrib>SAKO, Ryo</creatorcontrib><creatorcontrib>FURUSAWA, Masahiro</creatorcontrib><creatorcontrib>MURAMATSU, Takashi</creatorcontrib><title>Response to light compressive force in human cementoblasts in vitro</title><title>Biomedical Research</title><addtitle>Biomed. Res.</addtitle><description>The objective of this study is to investigate the responses of human cementoblasts to light compressive force in vitro. A human cementoblast cell line (HCEM) was loaded for 12 h by mounting coverslips (0.25 gf/cm2). The coverslips were removed and the cells were cultured for up to 21 days. Cells without glass loading were used as controls. Cell growth, morphological changes, and the mRNA expression of RUNX2, ALP, WNT5A and SPON1 were investigated. No significant differences were observed in cell numbers between the compressed group and control group. Morphology of the compressed cells was slightly flattened on day 0; however, no indications of cell death were detected. Expression of differentiation markers including RUNX2, ALP and WNT5A was significantly lower in the compressed group (0.7, 0.75 and 0.75-fold respectively, P < 0.05) than in the control group on day 7. The expression levels of SPON1, a differentiation marker of cementoblasts, were higher on days 7 and 14 than on day 0, but were lower in the compressed group than in the control group (P < 0.01). These results suggest that light compressive force does not affect cell growth and morphology, but restrains higher expression of cementogenic differentiation markers in human cementoblasts in vitro.</description><subject>Biomarkers</subject><subject>Cbfa-1 protein</subject><subject>Cell death</subject><subject>Cell differentiation</subject><subject>Cell growth</subject><subject>Cell Line</subject><subject>Cell morphology</subject><subject>Cementogenesis - genetics</subject><subject>Compressive Strength</subject><subject>Cytology</subject><subject>Dental Cementum - metabolism</subject><subject>Differentiation</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Morphology</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Studies</subject><subject>Wnt protein</subject><issn>0388-6107</issn><issn>1880-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpdkEFLJDEQRoMoOqvePS0NXrz0WEm6k_RRhl13QRBEwVtIx4rTQ3dnNkkP-O_NMLMDegqVevWo-gi5ojBnjMFt2_kB3wLGOZdz1vAjMqNKQckpfz0mM-BKlYKCPCM_YlxBrqnip-SMSakqJdmMLJ4wrv0YsUi-6Lv3ZSqsH9ZZGbsNFs4Hi0U3FstpMGNhccAx-bY3McXt96ZLwV-QE2f6iJf795y8_P71vPhTPjze_13cPZRWMEhl2xgLDOqWCaBN41zj0NimdkIadBVF2iipZNVyC5JxaFUL3DrL65qaCpCfk5uddx38vwlj0kMXLfa9GdFPUefbaiFFLURGr7-hKz-FMW-3pQQXUKsqU7CjbPAxBnR6HbrBhA9NQW8D1oeANZc6B5xHfu7FU5s7h4H_iWZgsQNWMZl3PAAmpM72-NVY77WHrl2aoHHkn7HtkXU</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>MATSUNAGA, Kenji</creator><creator>ITO, Chika</creator><creator>NAKAKOGAWA, Kaichi</creator><creator>SUGIUCHI, Akina</creator><creator>SAKO, Ryo</creator><creator>FURUSAWA, Masahiro</creator><creator>MURAMATSU, Takashi</creator><general>Biomedical Research Press</general><general>Japan Science and Technology Agency</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>7QO</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20160101</creationdate><title>Response to light compressive force in human cementoblasts in vitro</title><author>MATSUNAGA, Kenji ; ITO, Chika ; NAKAKOGAWA, Kaichi ; SUGIUCHI, Akina ; SAKO, Ryo ; FURUSAWA, Masahiro ; MURAMATSU, Takashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c620t-b9ac0205b260199ff9feac95f67aef41e1987874b3c07230b8b03cfc3551a40e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Biomarkers</topic><topic>Cbfa-1 protein</topic><topic>Cell death</topic><topic>Cell differentiation</topic><topic>Cell growth</topic><topic>Cell Line</topic><topic>Cell morphology</topic><topic>Cementogenesis - genetics</topic><topic>Compressive Strength</topic><topic>Cytology</topic><topic>Dental Cementum - metabolism</topic><topic>Differentiation</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Morphology</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Studies</topic><topic>Wnt protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MATSUNAGA, Kenji</creatorcontrib><creatorcontrib>ITO, Chika</creatorcontrib><creatorcontrib>NAKAKOGAWA, Kaichi</creatorcontrib><creatorcontrib>SUGIUCHI, Akina</creatorcontrib><creatorcontrib>SAKO, Ryo</creatorcontrib><creatorcontrib>FURUSAWA, Masahiro</creatorcontrib><creatorcontrib>MURAMATSU, Takashi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biomedical Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MATSUNAGA, Kenji</au><au>ITO, Chika</au><au>NAKAKOGAWA, Kaichi</au><au>SUGIUCHI, Akina</au><au>SAKO, Ryo</au><au>FURUSAWA, Masahiro</au><au>MURAMATSU, Takashi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Response to light compressive force in human cementoblasts in vitro</atitle><jtitle>Biomedical Research</jtitle><addtitle>Biomed. 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Expression of differentiation markers including RUNX2, ALP and WNT5A was significantly lower in the compressed group (0.7, 0.75 and 0.75-fold respectively, P < 0.05) than in the control group on day 7. The expression levels of SPON1, a differentiation marker of cementoblasts, were higher on days 7 and 14 than on day 0, but were lower in the compressed group than in the control group (P < 0.01). These results suggest that light compressive force does not affect cell growth and morphology, but restrains higher expression of cementogenic differentiation markers in human cementoblasts in vitro.</abstract><cop>Japan</cop><pub>Biomedical Research Press</pub><pmid>27784872</pmid><doi>10.2220/biomedres.37.293</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers Cbfa-1 protein Cell death Cell differentiation Cell growth Cell Line Cell morphology Cementogenesis - genetics Compressive Strength Cytology Dental Cementum - metabolism Differentiation Gene expression Gene Expression Regulation Humans In Vitro Techniques Morphology RNA, Messenger - genetics RNA, Messenger - metabolism Studies Wnt protein |
title | Response to light compressive force in human cementoblasts in vitro |
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