Epidermal Cell Surface Structure and Chitin-Protein Co-assembly Determine Fiber Architecture in the Locust Cuticle
The geometrical similarity of helicoidal fiber arrangement in many biological fibrous extracellular matrices, such as bone, plant cell wall, or arthropod cuticle, to that of cholesteric liquid mesophases has led to the hypothesis that they may form passively through a mesophase precursor rather than...
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Veröffentlicht in: | ACS applied materials & interfaces 2020-06, Vol.12 (23), p.25581-25590 |
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creator | Sviben, Sanja Spaeker, Oliver Bennet, Mathieu Albéric, Marie Dirks, Jan-Henning Moussian, Bernard Fratzl, Peter Bertinetti, Luca Politi, Yael |
description | The geometrical similarity of helicoidal fiber arrangement in many biological fibrous extracellular matrices, such as bone, plant cell wall, or arthropod cuticle, to that of cholesteric liquid mesophases has led to the hypothesis that they may form passively through a mesophase precursor rather than by direct cellular control. In search of direct evidence to support or refute this hypothesis, here, we studied the process of cuticle formation in the tibia of the migratory locust,
, where daily growth layers arise by the deposition of fiber arrangements alternating between unidirectional and helicoidal structures. Using focused ion beam/scanning electron microscopy (FIB/SEM) volume imaging and scanning X-ray scattering, we show that the epidermal cells determine an initial fiber orientation, from which the final architecture emerges by the self-organized co-assembly of chitin and proteins. Fiber orientation in the locust cuticle is therefore determined by both active and passive processes. |
doi_str_mv | 10.1021/acsami.0c04572 |
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, where daily growth layers arise by the deposition of fiber arrangements alternating between unidirectional and helicoidal structures. Using focused ion beam/scanning electron microscopy (FIB/SEM) volume imaging and scanning X-ray scattering, we show that the epidermal cells determine an initial fiber orientation, from which the final architecture emerges by the self-organized co-assembly of chitin and proteins. Fiber orientation in the locust cuticle is therefore determined by both active and passive processes.</description><identifier>ISSN: 1944-8244</identifier><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.0c04572</identifier><identifier>PMID: 32343541</identifier><language>eng</language><publisher>United States: Washington, D.C. : American Chemical Society</publisher><subject>Analytical chemistry ; Animal Shells - metabolism ; Animal Shells - ultrastructure ; Animals ; Biochemistry, Molecular Biology ; Chemical Sciences ; Chitin - metabolism ; Epidermal Cells - metabolism ; Epidermal Cells - ultrastructure ; Insect Proteins - metabolism ; Life Sciences ; Locusta migratoria - growth & development ; Locusta migratoria - metabolism ; Machine Learning ; Microscopy, Electron, Scanning ; Microvilli - metabolism ; Scattering, Radiation ; Structural Biology ; X-Rays</subject><ispartof>ACS applied materials & interfaces, 2020-06, Vol.12 (23), p.25581-25590</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2020 American Chemical Society 2020 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-1b623c77ba45177418465796746569c4be36d0f7437f4594d689868ae559b7093</citedby><cites>FETCH-LOGICAL-c490t-1b623c77ba45177418465796746569c4be36d0f7437f4594d689868ae559b7093</cites><orcidid>0000-0002-4666-9610 ; 0000-0002-5322-9904 ; 0000-0002-2872-8277</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,2752,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32343541$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.sorbonne-universite.fr/hal-03066445$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Sviben, Sanja</creatorcontrib><creatorcontrib>Spaeker, Oliver</creatorcontrib><creatorcontrib>Bennet, Mathieu</creatorcontrib><creatorcontrib>Albéric, Marie</creatorcontrib><creatorcontrib>Dirks, Jan-Henning</creatorcontrib><creatorcontrib>Moussian, Bernard</creatorcontrib><creatorcontrib>Fratzl, Peter</creatorcontrib><creatorcontrib>Bertinetti, Luca</creatorcontrib><creatorcontrib>Politi, Yael</creatorcontrib><title>Epidermal Cell Surface Structure and Chitin-Protein Co-assembly Determine Fiber Architecture in the Locust Cuticle</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl Mater Interfaces</addtitle><description>The geometrical similarity of helicoidal fiber arrangement in many biological fibrous extracellular matrices, such as bone, plant cell wall, or arthropod cuticle, to that of cholesteric liquid mesophases has led to the hypothesis that they may form passively through a mesophase precursor rather than by direct cellular control. In search of direct evidence to support or refute this hypothesis, here, we studied the process of cuticle formation in the tibia of the migratory locust,
, where daily growth layers arise by the deposition of fiber arrangements alternating between unidirectional and helicoidal structures. Using focused ion beam/scanning electron microscopy (FIB/SEM) volume imaging and scanning X-ray scattering, we show that the epidermal cells determine an initial fiber orientation, from which the final architecture emerges by the self-organized co-assembly of chitin and proteins. Fiber orientation in the locust cuticle is therefore determined by both active and passive processes.</description><subject>Analytical chemistry</subject><subject>Animal Shells - metabolism</subject><subject>Animal Shells - ultrastructure</subject><subject>Animals</subject><subject>Biochemistry, Molecular Biology</subject><subject>Chemical Sciences</subject><subject>Chitin - metabolism</subject><subject>Epidermal Cells - metabolism</subject><subject>Epidermal Cells - ultrastructure</subject><subject>Insect Proteins - metabolism</subject><subject>Life Sciences</subject><subject>Locusta migratoria - growth & development</subject><subject>Locusta migratoria - metabolism</subject><subject>Machine Learning</subject><subject>Microscopy, Electron, Scanning</subject><subject>Microvilli - metabolism</subject><subject>Scattering, Radiation</subject><subject>Structural Biology</subject><subject>X-Rays</subject><issn>1944-8244</issn><issn>1944-8252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc1rFTEUxYMottZuXUqWuphnvjPZCI-xtcKDFmrXIZO544vMxzPJFPrfmzLPh7o6Ifmdc7k5CL2jZEMJo5-cT24MG-KJkJq9QOfUCFHVTLKXp7MQZ-hNSj8JUZwR-RqdccYFl4Keo3h1CB3E0Q24gWHA90vsnQd8n-Pi8xIBu6nDzT7kMFV3cc4QJtzMlUsJxnZ4wl8gF3uYAF-HFiLeRl9gWL2FzXvAu9kvKeNmycEP8Ba96t2Q4PKoF-jh-up7c1Ptbr9-a7a7ygtDckVbxbjXunVCUq0FrYWS2ihdRBkvWuCqI70WXPdCGtGp2tSqdiClaTUx_AJ9XnMPSztC52HK0Q32EMPo4pOdXbD_vkxhb3_Mj1ZzImrGS8DHNWD_n-1mu7PPd4QTpYSQj7SwH47D4vxrgZTtGJIvP-ommJdkGTeKF16zgm5W1Mc5pQj9KZsS-1yqXUu1x1KL4f3fi5zwPy3y344unjc</recordid><startdate>20200610</startdate><enddate>20200610</enddate><creator>Sviben, Sanja</creator><creator>Spaeker, Oliver</creator><creator>Bennet, Mathieu</creator><creator>Albéric, Marie</creator><creator>Dirks, Jan-Henning</creator><creator>Moussian, Bernard</creator><creator>Fratzl, Peter</creator><creator>Bertinetti, Luca</creator><creator>Politi, Yael</creator><general>Washington, D.C. : American Chemical Society</general><general>American Chemical Society</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>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4666-9610</orcidid><orcidid>https://orcid.org/0000-0002-5322-9904</orcidid><orcidid>https://orcid.org/0000-0002-2872-8277</orcidid></search><sort><creationdate>20200610</creationdate><title>Epidermal Cell Surface Structure and Chitin-Protein Co-assembly Determine Fiber Architecture in the Locust Cuticle</title><author>Sviben, Sanja ; Spaeker, Oliver ; Bennet, Mathieu ; Albéric, Marie ; Dirks, Jan-Henning ; Moussian, Bernard ; Fratzl, Peter ; Bertinetti, Luca ; Politi, Yael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-1b623c77ba45177418465796746569c4be36d0f7437f4594d689868ae559b7093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Analytical chemistry</topic><topic>Animal Shells - metabolism</topic><topic>Animal Shells - ultrastructure</topic><topic>Animals</topic><topic>Biochemistry, Molecular Biology</topic><topic>Chemical Sciences</topic><topic>Chitin - metabolism</topic><topic>Epidermal Cells - metabolism</topic><topic>Epidermal Cells - ultrastructure</topic><topic>Insect Proteins - metabolism</topic><topic>Life Sciences</topic><topic>Locusta migratoria - growth & development</topic><topic>Locusta migratoria - metabolism</topic><topic>Machine Learning</topic><topic>Microscopy, Electron, Scanning</topic><topic>Microvilli - metabolism</topic><topic>Scattering, Radiation</topic><topic>Structural Biology</topic><topic>X-Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sviben, Sanja</creatorcontrib><creatorcontrib>Spaeker, Oliver</creatorcontrib><creatorcontrib>Bennet, Mathieu</creatorcontrib><creatorcontrib>Albéric, Marie</creatorcontrib><creatorcontrib>Dirks, Jan-Henning</creatorcontrib><creatorcontrib>Moussian, Bernard</creatorcontrib><creatorcontrib>Fratzl, Peter</creatorcontrib><creatorcontrib>Bertinetti, Luca</creatorcontrib><creatorcontrib>Politi, Yael</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>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>ACS applied materials & interfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sviben, Sanja</au><au>Spaeker, Oliver</au><au>Bennet, Mathieu</au><au>Albéric, Marie</au><au>Dirks, Jan-Henning</au><au>Moussian, Bernard</au><au>Fratzl, Peter</au><au>Bertinetti, Luca</au><au>Politi, Yael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epidermal Cell Surface Structure and Chitin-Protein Co-assembly Determine Fiber Architecture in the Locust Cuticle</atitle><jtitle>ACS applied materials & interfaces</jtitle><addtitle>ACS Appl Mater Interfaces</addtitle><date>2020-06-10</date><risdate>2020</risdate><volume>12</volume><issue>23</issue><spage>25581</spage><epage>25590</epage><pages>25581-25590</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><abstract>The geometrical similarity of helicoidal fiber arrangement in many biological fibrous extracellular matrices, such as bone, plant cell wall, or arthropod cuticle, to that of cholesteric liquid mesophases has led to the hypothesis that they may form passively through a mesophase precursor rather than by direct cellular control. In search of direct evidence to support or refute this hypothesis, here, we studied the process of cuticle formation in the tibia of the migratory locust,
, where daily growth layers arise by the deposition of fiber arrangements alternating between unidirectional and helicoidal structures. Using focused ion beam/scanning electron microscopy (FIB/SEM) volume imaging and scanning X-ray scattering, we show that the epidermal cells determine an initial fiber orientation, from which the final architecture emerges by the self-organized co-assembly of chitin and proteins. Fiber orientation in the locust cuticle is therefore determined by both active and passive processes.</abstract><cop>United States</cop><pub>Washington, D.C. : American Chemical Society</pub><pmid>32343541</pmid><doi>10.1021/acsami.0c04572</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-4666-9610</orcidid><orcidid>https://orcid.org/0000-0002-5322-9904</orcidid><orcidid>https://orcid.org/0000-0002-2872-8277</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analytical chemistry Animal Shells - metabolism Animal Shells - ultrastructure Animals Biochemistry, Molecular Biology Chemical Sciences Chitin - metabolism Epidermal Cells - metabolism Epidermal Cells - ultrastructure Insect Proteins - metabolism Life Sciences Locusta migratoria - growth & development Locusta migratoria - metabolism Machine Learning Microscopy, Electron, Scanning Microvilli - metabolism Scattering, Radiation Structural Biology X-Rays |
title | Epidermal Cell Surface Structure and Chitin-Protein Co-assembly Determine Fiber Architecture in the Locust Cuticle |
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