Neuron-like differentiation of mesenchymal stem cells on silicon nanowires
The behavior of mammalian cells on vertical nanowire (NW) arrays, including cell spreading and the dynamic distribution of focal adhesions and cytoskeletal proteins, has been intensively studied to extend the implications for cellular manipulations in vitro. Prompted by the result that cells on sili...
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creator | Kim, Hyunju Kim, Ilsoo Choi, Heon-Jin Kim, So Yeon Yang, Eun Gyeong |
description | The behavior of mammalian cells on vertical nanowire (NW) arrays, including cell spreading and the dynamic distribution of focal adhesions and cytoskeletal proteins, has been intensively studied to extend the implications for cellular manipulations in vitro. Prompted by the result that cells on silicon (Si) NWs showed morphological changes and reduced migration rates, we have explored the transition of mesenchymal stem cells into a neuronal lineage by using SiNWs with varying lengths. When human mesenchymal stem cells (hMSCs) were cultured on the longest SiNWs for 3 days, most of the cells exhibited elongated shapes with neurite-like extensions and dot-like focal adhesions that were prominently observed along with actin filaments. Under these circumstances, the cell motility analyzed by live cell imaging was found to decrease due to the presence of SiNWs. In addition, the slowed growth rate, as well as the reduced population of S phase cells, suggested that the cell cycle was likely arrested in response to the differentiation process. Furthermore, we measured the mRNA levels of several lineage-specific markers to confirm that the SiNWs actually induced neuron-like differentiation of the hMSCs while hampering their osteogenic differentiation. Taken together, our results implied that SiNWs were capable of inducing active reorganization of cellular behaviors, collectively guiding the fate of hMSCs into the neural lineage even in the absence of any inducing reagent. |
doi_str_mv | 10.1039/c5nr05787f |
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Prompted by the result that cells on silicon (Si) NWs showed morphological changes and reduced migration rates, we have explored the transition of mesenchymal stem cells into a neuronal lineage by using SiNWs with varying lengths. When human mesenchymal stem cells (hMSCs) were cultured on the longest SiNWs for 3 days, most of the cells exhibited elongated shapes with neurite-like extensions and dot-like focal adhesions that were prominently observed along with actin filaments. Under these circumstances, the cell motility analyzed by live cell imaging was found to decrease due to the presence of SiNWs. In addition, the slowed growth rate, as well as the reduced population of S phase cells, suggested that the cell cycle was likely arrested in response to the differentiation process. Furthermore, we measured the mRNA levels of several lineage-specific markers to confirm that the SiNWs actually induced neuron-like differentiation of the hMSCs while hampering their osteogenic differentiation. Taken together, our results implied that SiNWs were capable of inducing active reorganization of cellular behaviors, collectively guiding the fate of hMSCs into the neural lineage even in the absence of any inducing reagent.</description><identifier>ISSN: 2040-3364</identifier><identifier>EISSN: 2040-3372</identifier><identifier>DOI: 10.1039/c5nr05787f</identifier><identifier>PMID: 26422757</identifier><language>eng</language><publisher>England</publisher><subject>Adhesion ; Antigens, Differentiation - biosynthesis ; Arrays ; Cell Differentiation ; Cell Line ; Cellular ; Differentiation ; Gene Expression Regulation ; Humans ; Mesenchymal Stromal Cells - cytology ; Mesenchymal Stromal Cells - metabolism ; Nanostructure ; Nanowires ; Nanowires - chemistry ; Neurons - cytology ; Neurons - metabolism ; RNA, Messenger - biosynthesis ; Silicon ; Silicon - chemistry ; Stem cells</subject><ispartof>Nanoscale, 2015-10, Vol.7 (40), p.17131-17138</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-aa271a63124b62d83e7df0e8580ab4771b233fa71797aee2460f7dc0c00298d03</citedby><cites>FETCH-LOGICAL-c390t-aa271a63124b62d83e7df0e8580ab4771b233fa71797aee2460f7dc0c00298d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26422757$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Hyunju</creatorcontrib><creatorcontrib>Kim, Ilsoo</creatorcontrib><creatorcontrib>Choi, Heon-Jin</creatorcontrib><creatorcontrib>Kim, So Yeon</creatorcontrib><creatorcontrib>Yang, Eun Gyeong</creatorcontrib><title>Neuron-like differentiation of mesenchymal stem cells on silicon nanowires</title><title>Nanoscale</title><addtitle>Nanoscale</addtitle><description>The behavior of mammalian cells on vertical nanowire (NW) arrays, including cell spreading and the dynamic distribution of focal adhesions and cytoskeletal proteins, has been intensively studied to extend the implications for cellular manipulations in vitro. Prompted by the result that cells on silicon (Si) NWs showed morphological changes and reduced migration rates, we have explored the transition of mesenchymal stem cells into a neuronal lineage by using SiNWs with varying lengths. When human mesenchymal stem cells (hMSCs) were cultured on the longest SiNWs for 3 days, most of the cells exhibited elongated shapes with neurite-like extensions and dot-like focal adhesions that were prominently observed along with actin filaments. Under these circumstances, the cell motility analyzed by live cell imaging was found to decrease due to the presence of SiNWs. In addition, the slowed growth rate, as well as the reduced population of S phase cells, suggested that the cell cycle was likely arrested in response to the differentiation process. Furthermore, we measured the mRNA levels of several lineage-specific markers to confirm that the SiNWs actually induced neuron-like differentiation of the hMSCs while hampering their osteogenic differentiation. Taken together, our results implied that SiNWs were capable of inducing active reorganization of cellular behaviors, collectively guiding the fate of hMSCs into the neural lineage even in the absence of any inducing reagent.</description><subject>Adhesion</subject><subject>Antigens, Differentiation - biosynthesis</subject><subject>Arrays</subject><subject>Cell Differentiation</subject><subject>Cell Line</subject><subject>Cellular</subject><subject>Differentiation</subject><subject>Gene Expression Regulation</subject><subject>Humans</subject><subject>Mesenchymal Stromal Cells - cytology</subject><subject>Mesenchymal Stromal Cells - metabolism</subject><subject>Nanostructure</subject><subject>Nanowires</subject><subject>Nanowires - chemistry</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Silicon</subject><subject>Silicon - chemistry</subject><subject>Stem cells</subject><issn>2040-3364</issn><issn>2040-3372</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV1LwzAUhoMobk5v_AHSSxGqJ0mbNJcynB-MCaLXJUtPMNqmM2mR_Xs7nbve1XvgPLznwEPIOYVrClzdmNwHyGUh7QEZM8gg5Vyyw90sshE5ifEDQCgu-DEZMZExJnM5Jk8L7EPr09p9YlI5azGg75zuXOuT1iYNRvTmfd3oOokdNonBuo7JsIyudmZIr3377QLGU3JkdR3xbJsT8ja7e50-pPPn-8fp7Tw1XEGXas0k1YJTli0FqwqOsrKARV6AXmZS0iXj3GpJpZIakWUCrKwMGACmigr4hFz-9a5C-9Vj7MrGxc1b2mPbx5JKUeSS8YLvgzJQMBzdA2WU50ypDXr1h5rQxhjQlqvgGh3WJYVyY6Sc5ouXXyOzAb7Y9vbLBqsd-q-A_wA91YUb</recordid><startdate>20151028</startdate><enddate>20151028</enddate><creator>Kim, Hyunju</creator><creator>Kim, Ilsoo</creator><creator>Choi, Heon-Jin</creator><creator>Kim, So Yeon</creator><creator>Yang, Eun Gyeong</creator><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><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope><scope>7TK</scope></search><sort><creationdate>20151028</creationdate><title>Neuron-like differentiation of mesenchymal stem cells on silicon nanowires</title><author>Kim, Hyunju ; Kim, Ilsoo ; Choi, Heon-Jin ; Kim, So Yeon ; Yang, Eun Gyeong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-aa271a63124b62d83e7df0e8580ab4771b233fa71797aee2460f7dc0c00298d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adhesion</topic><topic>Antigens, Differentiation - biosynthesis</topic><topic>Arrays</topic><topic>Cell Differentiation</topic><topic>Cell Line</topic><topic>Cellular</topic><topic>Differentiation</topic><topic>Gene Expression Regulation</topic><topic>Humans</topic><topic>Mesenchymal Stromal Cells - cytology</topic><topic>Mesenchymal Stromal Cells - metabolism</topic><topic>Nanostructure</topic><topic>Nanowires</topic><topic>Nanowires - chemistry</topic><topic>Neurons - cytology</topic><topic>Neurons - metabolism</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Silicon</topic><topic>Silicon - chemistry</topic><topic>Stem cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Hyunju</creatorcontrib><creatorcontrib>Kim, Ilsoo</creatorcontrib><creatorcontrib>Choi, Heon-Jin</creatorcontrib><creatorcontrib>Kim, So Yeon</creatorcontrib><creatorcontrib>Yang, Eun Gyeong</creatorcontrib><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><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Neurosciences Abstracts</collection><jtitle>Nanoscale</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Hyunju</au><au>Kim, Ilsoo</au><au>Choi, Heon-Jin</au><au>Kim, So Yeon</au><au>Yang, Eun Gyeong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuron-like differentiation of mesenchymal stem cells on silicon nanowires</atitle><jtitle>Nanoscale</jtitle><addtitle>Nanoscale</addtitle><date>2015-10-28</date><risdate>2015</risdate><volume>7</volume><issue>40</issue><spage>17131</spage><epage>17138</epage><pages>17131-17138</pages><issn>2040-3364</issn><eissn>2040-3372</eissn><abstract>The behavior of mammalian cells on vertical nanowire (NW) arrays, including cell spreading and the dynamic distribution of focal adhesions and cytoskeletal proteins, has been intensively studied to extend the implications for cellular manipulations in vitro. Prompted by the result that cells on silicon (Si) NWs showed morphological changes and reduced migration rates, we have explored the transition of mesenchymal stem cells into a neuronal lineage by using SiNWs with varying lengths. When human mesenchymal stem cells (hMSCs) were cultured on the longest SiNWs for 3 days, most of the cells exhibited elongated shapes with neurite-like extensions and dot-like focal adhesions that were prominently observed along with actin filaments. Under these circumstances, the cell motility analyzed by live cell imaging was found to decrease due to the presence of SiNWs. In addition, the slowed growth rate, as well as the reduced population of S phase cells, suggested that the cell cycle was likely arrested in response to the differentiation process. Furthermore, we measured the mRNA levels of several lineage-specific markers to confirm that the SiNWs actually induced neuron-like differentiation of the hMSCs while hampering their osteogenic differentiation. Taken together, our results implied that SiNWs were capable of inducing active reorganization of cellular behaviors, collectively guiding the fate of hMSCs into the neural lineage even in the absence of any inducing reagent.</abstract><cop>England</cop><pmid>26422757</pmid><doi>10.1039/c5nr05787f</doi><tpages>8</tpages></addata></record> |
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source | MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Adhesion Antigens, Differentiation - biosynthesis Arrays Cell Differentiation Cell Line Cellular Differentiation Gene Expression Regulation Humans Mesenchymal Stromal Cells - cytology Mesenchymal Stromal Cells - metabolism Nanostructure Nanowires Nanowires - chemistry Neurons - cytology Neurons - metabolism RNA, Messenger - biosynthesis Silicon Silicon - chemistry Stem cells |
title | Neuron-like differentiation of mesenchymal stem cells on silicon nanowires |
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