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Human dermal fibroblast migration induced by fibronectin in autocrine and paracrine manners
Although fibronectin (FN) is known as a chemoattractant for human dermal fibroblasts (HDFs), it is unclear whether HDF migration is stimulated by FN produced by HDFs (autocrine manner) or by keratinocytes (paracrine manner). In this study, we investigated HDF migration by Boyden chamber assay using...
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Published in: | Experimental dermatology 2014-09, Vol.23 (9), p.682-684 |
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creator | Li, Xiaoguang Qian, Hua Ono, Fumitake Tsuchisaka, Atsunari Krol, Rafal P. Ohara, Koji Hayakawa, Taihei Matsueda, Satoko Sasada, Tetsuro Ohata, Chika Furumura, Minao Hamada, Takahiro Hashimoto, Takashi |
description | Although fibronectin (FN) is known as a chemoattractant for human dermal fibroblasts (HDFs), it is unclear whether HDF migration is stimulated by FN produced by HDFs (autocrine manner) or by keratinocytes (paracrine manner). In this study, we investigated HDF migration by Boyden chamber assay using conditioned media from HDFs and HaCaT cells (keratinocyte cell line). Immunoblotting and enzyme‐linked immunosorbent assay revealed that FN existed in both conditioned media. Boyden chamber assay showed both conditioned media stimulated HDF migration, which was inhibited by anti‐FN antibody. Antibodies to both integrin β1and β3 subunits inhibited HDF migration induced by HDF‐conditioned medium almost completely and that by HaCaT cell‐conditioned medium with 50–60%. These results suggested that HDF migration was stimulated by FN in both autocrine and paracrine manners. However, the mechanisms of HDF migration by FN, particularly the role of integrin β1 and β3 subunits, were slightly different between autocrine and paracrine manners. |
doi_str_mv | 10.1111/exd.12447 |
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In this study, we investigated HDF migration by Boyden chamber assay using conditioned media from HDFs and HaCaT cells (keratinocyte cell line). Immunoblotting and enzyme‐linked immunosorbent assay revealed that FN existed in both conditioned media. Boyden chamber assay showed both conditioned media stimulated HDF migration, which was inhibited by anti‐FN antibody. Antibodies to both integrin β1and β3 subunits inhibited HDF migration induced by HDF‐conditioned medium almost completely and that by HaCaT cell‐conditioned medium with 50–60%. These results suggested that HDF migration was stimulated by FN in both autocrine and paracrine manners. However, the mechanisms of HDF migration by FN, particularly the role of integrin β1 and β3 subunits, were slightly different between autocrine and paracrine manners.</description><identifier>ISSN: 0906-6705</identifier><identifier>EISSN: 1600-0625</identifier><identifier>DOI: 10.1111/exd.12447</identifier><identifier>PMID: 24828603</identifier><language>eng</language><publisher>Denmark: Blackwell Publishing Ltd</publisher><subject>Autocrine Communication ; Cell Line ; cell migration ; Cell Movement - physiology ; Culture Media, Conditioned ; Fibroblasts - physiology ; fibronectin ; Fibronectins - physiology ; human dermal fibroblasts ; Humans ; integrin ; Integrin beta1 - physiology ; Integrin beta3 - physiology ; Keratinocytes - physiology ; Paracrine Communication ; Skin - cytology ; Skin Physiological Phenomena</subject><ispartof>Experimental dermatology, 2014-09, Vol.23 (9), p.682-684</ispartof><rights>2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4647-3bd885505f1559db8a808df8d8372a96522161c39532c7b7375d985ab00f79903</citedby><cites>FETCH-LOGICAL-c4647-3bd885505f1559db8a808df8d8372a96522161c39532c7b7375d985ab00f79903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24828603$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Xiaoguang</creatorcontrib><creatorcontrib>Qian, Hua</creatorcontrib><creatorcontrib>Ono, Fumitake</creatorcontrib><creatorcontrib>Tsuchisaka, Atsunari</creatorcontrib><creatorcontrib>Krol, Rafal P.</creatorcontrib><creatorcontrib>Ohara, Koji</creatorcontrib><creatorcontrib>Hayakawa, Taihei</creatorcontrib><creatorcontrib>Matsueda, Satoko</creatorcontrib><creatorcontrib>Sasada, Tetsuro</creatorcontrib><creatorcontrib>Ohata, Chika</creatorcontrib><creatorcontrib>Furumura, Minao</creatorcontrib><creatorcontrib>Hamada, Takahiro</creatorcontrib><creatorcontrib>Hashimoto, Takashi</creatorcontrib><title>Human dermal fibroblast migration induced by fibronectin in autocrine and paracrine manners</title><title>Experimental dermatology</title><addtitle>Exp Dermatol</addtitle><description>Although fibronectin (FN) is known as a chemoattractant for human dermal fibroblasts (HDFs), it is unclear whether HDF migration is stimulated by FN produced by HDFs (autocrine manner) or by keratinocytes (paracrine manner). In this study, we investigated HDF migration by Boyden chamber assay using conditioned media from HDFs and HaCaT cells (keratinocyte cell line). Immunoblotting and enzyme‐linked immunosorbent assay revealed that FN existed in both conditioned media. Boyden chamber assay showed both conditioned media stimulated HDF migration, which was inhibited by anti‐FN antibody. Antibodies to both integrin β1and β3 subunits inhibited HDF migration induced by HDF‐conditioned medium almost completely and that by HaCaT cell‐conditioned medium with 50–60%. These results suggested that HDF migration was stimulated by FN in both autocrine and paracrine manners. However, the mechanisms of HDF migration by FN, particularly the role of integrin β1 and β3 subunits, were slightly different between autocrine and paracrine manners.</description><subject>Autocrine Communication</subject><subject>Cell Line</subject><subject>cell migration</subject><subject>Cell Movement - physiology</subject><subject>Culture Media, Conditioned</subject><subject>Fibroblasts - physiology</subject><subject>fibronectin</subject><subject>Fibronectins - physiology</subject><subject>human dermal fibroblasts</subject><subject>Humans</subject><subject>integrin</subject><subject>Integrin beta1 - physiology</subject><subject>Integrin beta3 - physiology</subject><subject>Keratinocytes - physiology</subject><subject>Paracrine Communication</subject><subject>Skin - cytology</subject><subject>Skin Physiological Phenomena</subject><issn>0906-6705</issn><issn>1600-0625</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp1kD1PwzAQhi0EoqUw8AdQRhjS2nH8kRGV0iIqWApFMFhO7CBD4hQ7Ee2_JyWlG15Ovnvuke4F4BzBIWrfSK_VEEVxzA5AH1EIQ0gjcgj6MIE0pAySHjjx_gNCxDAjx6AXxTziFOI-eJs1pbSB0q6URZCb1FVpIX0dlObdydpUNjBWNZlWQbrp5lZntdm2A9nUVeaM1YG0KlhJJ7tfa7Ta-VNwlMvC67NdHYCn28liPAvnj9O78fU8zGIasxCninNCIMkRIYlKueSQq5wrjlkkE0qiCFGU4YTgKGPp9gSVcCJTCHOWJBAPwGXnXbnqq9G-FqXxmS4KaXXVeIEIRQlljOEWverQzFXeO52LlTOldBuBoNhmKdosxW-WLXux0zZpqdWe_AuvBUYd8G0KvfnfJCYvN3_KsNswvtbr_YZ0n4Ju7xLLh6lYvNLF8vl-Jhj-AU90jKE</recordid><startdate>201409</startdate><enddate>201409</enddate><creator>Li, Xiaoguang</creator><creator>Qian, Hua</creator><creator>Ono, Fumitake</creator><creator>Tsuchisaka, Atsunari</creator><creator>Krol, Rafal P.</creator><creator>Ohara, Koji</creator><creator>Hayakawa, Taihei</creator><creator>Matsueda, Satoko</creator><creator>Sasada, Tetsuro</creator><creator>Ohata, Chika</creator><creator>Furumura, Minao</creator><creator>Hamada, Takahiro</creator><creator>Hashimoto, Takashi</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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>7X8</scope></search><sort><creationdate>201409</creationdate><title>Human dermal fibroblast migration induced by fibronectin in autocrine and paracrine manners</title><author>Li, Xiaoguang ; Qian, Hua ; Ono, Fumitake ; Tsuchisaka, Atsunari ; Krol, Rafal P. ; Ohara, Koji ; Hayakawa, Taihei ; Matsueda, Satoko ; Sasada, Tetsuro ; Ohata, Chika ; Furumura, Minao ; Hamada, Takahiro ; Hashimoto, Takashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4647-3bd885505f1559db8a808df8d8372a96522161c39532c7b7375d985ab00f79903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Autocrine Communication</topic><topic>Cell Line</topic><topic>cell migration</topic><topic>Cell Movement - physiology</topic><topic>Culture Media, Conditioned</topic><topic>Fibroblasts - physiology</topic><topic>fibronectin</topic><topic>Fibronectins - physiology</topic><topic>human dermal fibroblasts</topic><topic>Humans</topic><topic>integrin</topic><topic>Integrin beta1 - physiology</topic><topic>Integrin beta3 - physiology</topic><topic>Keratinocytes - physiology</topic><topic>Paracrine Communication</topic><topic>Skin - cytology</topic><topic>Skin Physiological Phenomena</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xiaoguang</creatorcontrib><creatorcontrib>Qian, Hua</creatorcontrib><creatorcontrib>Ono, Fumitake</creatorcontrib><creatorcontrib>Tsuchisaka, Atsunari</creatorcontrib><creatorcontrib>Krol, Rafal P.</creatorcontrib><creatorcontrib>Ohara, Koji</creatorcontrib><creatorcontrib>Hayakawa, Taihei</creatorcontrib><creatorcontrib>Matsueda, Satoko</creatorcontrib><creatorcontrib>Sasada, Tetsuro</creatorcontrib><creatorcontrib>Ohata, Chika</creatorcontrib><creatorcontrib>Furumura, Minao</creatorcontrib><creatorcontrib>Hamada, Takahiro</creatorcontrib><creatorcontrib>Hashimoto, Takashi</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xiaoguang</au><au>Qian, Hua</au><au>Ono, Fumitake</au><au>Tsuchisaka, Atsunari</au><au>Krol, Rafal P.</au><au>Ohara, Koji</au><au>Hayakawa, Taihei</au><au>Matsueda, Satoko</au><au>Sasada, Tetsuro</au><au>Ohata, Chika</au><au>Furumura, Minao</au><au>Hamada, Takahiro</au><au>Hashimoto, Takashi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human dermal fibroblast migration induced by fibronectin in autocrine and paracrine manners</atitle><jtitle>Experimental dermatology</jtitle><addtitle>Exp Dermatol</addtitle><date>2014-09</date><risdate>2014</risdate><volume>23</volume><issue>9</issue><spage>682</spage><epage>684</epage><pages>682-684</pages><issn>0906-6705</issn><eissn>1600-0625</eissn><abstract>Although fibronectin (FN) is known as a chemoattractant for human dermal fibroblasts (HDFs), it is unclear whether HDF migration is stimulated by FN produced by HDFs (autocrine manner) or by keratinocytes (paracrine manner). In this study, we investigated HDF migration by Boyden chamber assay using conditioned media from HDFs and HaCaT cells (keratinocyte cell line). Immunoblotting and enzyme‐linked immunosorbent assay revealed that FN existed in both conditioned media. Boyden chamber assay showed both conditioned media stimulated HDF migration, which was inhibited by anti‐FN antibody. Antibodies to both integrin β1and β3 subunits inhibited HDF migration induced by HDF‐conditioned medium almost completely and that by HaCaT cell‐conditioned medium with 50–60%. These results suggested that HDF migration was stimulated by FN in both autocrine and paracrine manners. However, the mechanisms of HDF migration by FN, particularly the role of integrin β1 and β3 subunits, were slightly different between autocrine and paracrine manners.</abstract><cop>Denmark</cop><pub>Blackwell Publishing Ltd</pub><pmid>24828603</pmid><doi>10.1111/exd.12447</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Autocrine Communication Cell Line cell migration Cell Movement - physiology Culture Media, Conditioned Fibroblasts - physiology fibronectin Fibronectins - physiology human dermal fibroblasts Humans integrin Integrin beta1 - physiology Integrin beta3 - physiology Keratinocytes - physiology Paracrine Communication Skin - cytology Skin Physiological Phenomena |
title | Human dermal fibroblast migration induced by fibronectin in autocrine and paracrine manners |
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