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Epidermal Cell Surface Structure and Chitin–Protein Co-assembly Determine Fiber Architecture in the Locust Cuticle
[Image: see text] 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 pre...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304823/ https://www.ncbi.nlm.nih.gov/pubmed/32343541 http://dx.doi.org/10.1021/acsami.0c04572 |
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author | Sviben, Sanja Spaeker, Oliver Bennet, Mathieu Albéric, Marie Dirks, Jan-Henning Moussian, Bernard Fratzl, Peter Bertinetti, Luca Politi, Yael |
author_facet | Sviben, Sanja Spaeker, Oliver Bennet, Mathieu Albéric, Marie Dirks, Jan-Henning Moussian, Bernard Fratzl, Peter Bertinetti, Luca Politi, Yael |
author_sort | Sviben, Sanja |
collection | PubMed |
description | [Image: see text] 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, Locusta migratoria, 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. |
format | Online Article Text |
id | pubmed-7304823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73048232020-06-22 Epidermal Cell Surface Structure and Chitin–Protein Co-assembly Determine Fiber Architecture in the Locust Cuticle Sviben, Sanja Spaeker, Oliver Bennet, Mathieu Albéric, Marie Dirks, Jan-Henning Moussian, Bernard Fratzl, Peter Bertinetti, Luca Politi, Yael ACS Appl Mater Interfaces [Image: see text] 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, Locusta migratoria, 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. American Chemical Society 2020-04-28 2020-06-10 /pmc/articles/PMC7304823/ /pubmed/32343541 http://dx.doi.org/10.1021/acsami.0c04572 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Sviben, Sanja Spaeker, Oliver Bennet, Mathieu Albéric, Marie Dirks, Jan-Henning Moussian, Bernard Fratzl, Peter Bertinetti, Luca Politi, Yael Epidermal Cell Surface Structure and Chitin–Protein Co-assembly Determine Fiber Architecture in the Locust Cuticle |
title | Epidermal
Cell Surface Structure and Chitin–Protein
Co-assembly Determine Fiber Architecture in the Locust Cuticle |
title_full | Epidermal
Cell Surface Structure and Chitin–Protein
Co-assembly Determine Fiber Architecture in the Locust Cuticle |
title_fullStr | Epidermal
Cell Surface Structure and Chitin–Protein
Co-assembly Determine Fiber Architecture in the Locust Cuticle |
title_full_unstemmed | Epidermal
Cell Surface Structure and Chitin–Protein
Co-assembly Determine Fiber Architecture in the Locust Cuticle |
title_short | Epidermal
Cell Surface Structure and Chitin–Protein
Co-assembly Determine Fiber Architecture in the Locust Cuticle |
title_sort | epidermal
cell surface structure and chitin–protein
co-assembly determine fiber architecture in the locust cuticle |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304823/ https://www.ncbi.nlm.nih.gov/pubmed/32343541 http://dx.doi.org/10.1021/acsami.0c04572 |
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