Cell guidance by ultrafine topography in vitro
Laser holography and microelectronic fabrication techniques have been employed to make grating surfaces in fused quartz with ultrafine period (260 nm) in an attempt to mimic the topography of aligned fibrillar extracellular matrix (ECM), which, in the past, has been shown to affect the behaviour of...
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Veröffentlicht in: | Journal of cell science 1991-05, Vol.99 (1), p.73-77 |
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container_title | Journal of cell science |
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creator | CLARK, P CONNOLLY, P CURTIS, A. S. G DOW, J. A. T WILKINSON, C. D. W |
description | Laser holography and microelectronic fabrication techniques have been employed to make grating surfaces in fused quartz with ultrafine period (260 nm) in an attempt to mimic the topography of aligned fibrillar extracellular matrix (ECM), which, in the past, has been shown to affect the behaviour of cells in vitro and in vivo. The alignment of BHK cells, MDCK cells and chick embryo cerebral neurones on 260 nm period grating surfaces (130 nm grooves separated by 130 nm) of various depths (100, 210 and 400 nm) was examined. While all gratings aligned BHK cell populations, the degree of alignment was dependent on depth. The response of single MDCK cells to the grating patterns was both to align precisely to the direction of the gratings, and to elongate; only their elongation was depth-dependent. MDCK cells that were part of epithelial cell islands, and the outgrowth of neurites from chick embryo neurones, were mainly unaffected by the grating surfaces. It is clear that topography on this scale can control cell behaviour, but guidance of this type is strongly dependent on cell type and cell-cell interactions. |
doi_str_mv | 10.1242/jcs.99.1.73 |
format | Article |
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S. G ; DOW, J. A. T ; WILKINSON, C. D. W</creator><creatorcontrib>CLARK, P ; CONNOLLY, P ; CURTIS, A. S. G ; DOW, J. A. T ; WILKINSON, C. D. W</creatorcontrib><description>Laser holography and microelectronic fabrication techniques have been employed to make grating surfaces in fused quartz with ultrafine period (260 nm) in an attempt to mimic the topography of aligned fibrillar extracellular matrix (ECM), which, in the past, has been shown to affect the behaviour of cells in vitro and in vivo. The alignment of BHK cells, MDCK cells and chick embryo cerebral neurones on 260 nm period grating surfaces (130 nm grooves separated by 130 nm) of various depths (100, 210 and 400 nm) was examined. While all gratings aligned BHK cell populations, the degree of alignment was dependent on depth. The response of single MDCK cells to the grating patterns was both to align precisely to the direction of the gratings, and to elongate; only their elongation was depth-dependent. 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Psychology ; Holography - methods ; Lasers ; Microscopy, Electron, Scanning ; Molecular and cellular biology ; Motility and taxis ; Neurons - ultrastructure</subject><ispartof>Journal of cell science, 1991-05, Vol.99 (1), p.73-77</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c327t-5442f33c486c0ab1b15add196f50a74d2871d7c7d15bb683ed88d09f4432fd33</citedby><cites>FETCH-LOGICAL-c327t-5442f33c486c0ab1b15add196f50a74d2871d7c7d15bb683ed88d09f4432fd33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,3666,27906,27907</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4982066$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1757503$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CLARK, P</creatorcontrib><creatorcontrib>CONNOLLY, P</creatorcontrib><creatorcontrib>CURTIS, A. S. G</creatorcontrib><creatorcontrib>DOW, J. A. T</creatorcontrib><creatorcontrib>WILKINSON, C. D. W</creatorcontrib><title>Cell guidance by ultrafine topography in vitro</title><title>Journal of cell science</title><addtitle>J Cell Sci</addtitle><description>Laser holography and microelectronic fabrication techniques have been employed to make grating surfaces in fused quartz with ultrafine period (260 nm) in an attempt to mimic the topography of aligned fibrillar extracellular matrix (ECM), which, in the past, has been shown to affect the behaviour of cells in vitro and in vivo. The alignment of BHK cells, MDCK cells and chick embryo cerebral neurones on 260 nm period grating surfaces (130 nm grooves separated by 130 nm) of various depths (100, 210 and 400 nm) was examined. While all gratings aligned BHK cell populations, the degree of alignment was dependent on depth. The response of single MDCK cells to the grating patterns was both to align precisely to the direction of the gratings, and to elongate; only their elongation was depth-dependent. MDCK cells that were part of epithelial cell islands, and the outgrowth of neurites from chick embryo neurones, were mainly unaffected by the grating surfaces. It is clear that topography on this scale can control cell behaviour, but guidance of this type is strongly dependent on cell type and cell-cell interactions.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell physiology</subject><subject>Cells, Cultured</subject><subject>Chick Embryo</subject><subject>Cricetinae</subject><subject>Dogs</subject><subject>Epithelium - ultrastructure</subject><subject>Extracellular Matrix - ultrastructure</subject><subject>Fibroblasts - ultrastructure</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Holography - methods</subject><subject>Lasers</subject><subject>Microscopy, Electron, Scanning</subject><subject>Molecular and cellular biology</subject><subject>Motility and taxis</subject><subject>Neurons - ultrastructure</subject><issn>0021-9533</issn><issn>1477-9137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtLw0AURgdRaq2uXAtZiBtJnGduZinFFxTcdD9M5lGnpEmcSYT-e1NadHUX3-FwOQjdElwQyunT1qRCyoIUwM7QnHCAXBIG52iOMSW5FIxdoquUthhjoBJmaEZAgMBsjoqla5psMwarW-Oyep-NzRC1D63Lhq7vNlH3X_sstNlPGGJ3jS68bpK7Od0FWr--rJfv-erz7WP5vMoNozDkgnPqGTO8Kg3WNamJ0NYSWXqBNXBLKyAWDFgi6rqsmLNVZbH0nDPqLWML9HDU9rH7Hl0a1C4kM32qW9eNSQEVJaNSTuDjETSxSyk6r_oYdjruFcHqEEdNcZSUiig4aO9O2rHeOfvPHmtM-_1p18noxsepSUh_GJcVxWXJfgE2Xmtf</recordid><startdate>199105</startdate><enddate>199105</enddate><creator>CLARK, P</creator><creator>CONNOLLY, P</creator><creator>CURTIS, A. S. 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W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-5442f33c486c0ab1b15add196f50a74d2871d7c7d15bb683ed88d09f4432fd33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell physiology</topic><topic>Cells, Cultured</topic><topic>Chick Embryo</topic><topic>Cricetinae</topic><topic>Dogs</topic><topic>Epithelium - ultrastructure</topic><topic>Extracellular Matrix - ultrastructure</topic><topic>Fibroblasts - ultrastructure</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Holography - methods</topic><topic>Lasers</topic><topic>Microscopy, Electron, Scanning</topic><topic>Molecular and cellular biology</topic><topic>Motility and taxis</topic><topic>Neurons - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CLARK, P</creatorcontrib><creatorcontrib>CONNOLLY, P</creatorcontrib><creatorcontrib>CURTIS, A. S. G</creatorcontrib><creatorcontrib>DOW, J. A. T</creatorcontrib><creatorcontrib>WILKINSON, C. D. 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W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cell guidance by ultrafine topography in vitro</atitle><jtitle>Journal of cell science</jtitle><addtitle>J Cell Sci</addtitle><date>1991-05</date><risdate>1991</risdate><volume>99</volume><issue>1</issue><spage>73</spage><epage>77</epage><pages>73-77</pages><issn>0021-9533</issn><eissn>1477-9137</eissn><coden>JNCSAI</coden><abstract>Laser holography and microelectronic fabrication techniques have been employed to make grating surfaces in fused quartz with ultrafine period (260 nm) in an attempt to mimic the topography of aligned fibrillar extracellular matrix (ECM), which, in the past, has been shown to affect the behaviour of cells in vitro and in vivo. The alignment of BHK cells, MDCK cells and chick embryo cerebral neurones on 260 nm period grating surfaces (130 nm grooves separated by 130 nm) of various depths (100, 210 and 400 nm) was examined. While all gratings aligned BHK cell populations, the degree of alignment was dependent on depth. The response of single MDCK cells to the grating patterns was both to align precisely to the direction of the gratings, and to elongate; only their elongation was depth-dependent. MDCK cells that were part of epithelial cell islands, and the outgrowth of neurites from chick embryo neurones, were mainly unaffected by the grating surfaces. It is clear that topography on this scale can control cell behaviour, but guidance of this type is strongly dependent on cell type and cell-cell interactions.</abstract><cop>Cambridge</cop><pub>Company of Biologists</pub><pmid>1757503</pmid><doi>10.1242/jcs.99.1.73</doi><tpages>5</tpages></addata></record> |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Company of Biologists |
subjects | Animals Biological and medical sciences Cell physiology Cells, Cultured Chick Embryo Cricetinae Dogs Epithelium - ultrastructure Extracellular Matrix - ultrastructure Fibroblasts - ultrastructure Fundamental and applied biological sciences. Psychology Holography - methods Lasers Microscopy, Electron, Scanning Molecular and cellular biology Motility and taxis Neurons - ultrastructure |
title | Cell guidance by ultrafine topography in vitro |
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