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Mapping the Complex Morphology of Cell Interactions with Nanowire Substrates Using FIB-SEM

Using high resolution focused ion beam scanning electron microscopy (FIB-SEM) we study the details of cell-nanostructure interactions using serial block face imaging. 3T3 Fibroblast cellular monolayers are cultured on flat glass as a control surface and on two types of nanostructured scaffold substr...

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Autores principales: Wierzbicki, Rafał, Købler, Carsten, Jensen, Mikkel R. B., Łopacińska, Joanna, Schmidt, Michael S., Skolimowski, Maciej, Abeille, Fabien, Qvortrup, Klaus, Mølhave, Kristian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3541134/
https://www.ncbi.nlm.nih.gov/pubmed/23326412
http://dx.doi.org/10.1371/journal.pone.0053307
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author Wierzbicki, Rafał
Købler, Carsten
Jensen, Mikkel R. B.
Łopacińska, Joanna
Schmidt, Michael S.
Skolimowski, Maciej
Abeille, Fabien
Qvortrup, Klaus
Mølhave, Kristian
author_facet Wierzbicki, Rafał
Købler, Carsten
Jensen, Mikkel R. B.
Łopacińska, Joanna
Schmidt, Michael S.
Skolimowski, Maciej
Abeille, Fabien
Qvortrup, Klaus
Mølhave, Kristian
author_sort Wierzbicki, Rafał
collection PubMed
description Using high resolution focused ion beam scanning electron microscopy (FIB-SEM) we study the details of cell-nanostructure interactions using serial block face imaging. 3T3 Fibroblast cellular monolayers are cultured on flat glass as a control surface and on two types of nanostructured scaffold substrates made from silicon black (Nanograss) with low- and high nanowire density. After culturing for 72 hours the cells were fixed, heavy metal stained, embedded in resin, and processed with FIB-SEM block face imaging without removing the substrate. The sample preparation procedure, image acquisition and image post-processing were specifically optimised for cellular monolayers cultured on nanostructured substrates. Cells display a wide range of interactions with the nanostructures depending on the surface morphology, but also greatly varying from one cell to another on the same substrate, illustrating a wide phenotypic variability. Depending on the substrate and cell, we observe that cells could for instance: break the nanowires and engulf them, flatten the nanowires or simply reside on top of them. Given the complexity of interactions, we have categorised our observations and created an overview map. The results demonstrate that detailed nanoscale resolution images are required to begin understanding the wide variety of individual cells’ interactions with a structured substrate. The map will provide a framework for light microscopy studies of such interactions indicating what modes of interactions must be considered.
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spelling pubmed-35411342013-01-16 Mapping the Complex Morphology of Cell Interactions with Nanowire Substrates Using FIB-SEM Wierzbicki, Rafał Købler, Carsten Jensen, Mikkel R. B. Łopacińska, Joanna Schmidt, Michael S. Skolimowski, Maciej Abeille, Fabien Qvortrup, Klaus Mølhave, Kristian PLoS One Research Article Using high resolution focused ion beam scanning electron microscopy (FIB-SEM) we study the details of cell-nanostructure interactions using serial block face imaging. 3T3 Fibroblast cellular monolayers are cultured on flat glass as a control surface and on two types of nanostructured scaffold substrates made from silicon black (Nanograss) with low- and high nanowire density. After culturing for 72 hours the cells were fixed, heavy metal stained, embedded in resin, and processed with FIB-SEM block face imaging without removing the substrate. The sample preparation procedure, image acquisition and image post-processing were specifically optimised for cellular monolayers cultured on nanostructured substrates. Cells display a wide range of interactions with the nanostructures depending on the surface morphology, but also greatly varying from one cell to another on the same substrate, illustrating a wide phenotypic variability. Depending on the substrate and cell, we observe that cells could for instance: break the nanowires and engulf them, flatten the nanowires or simply reside on top of them. Given the complexity of interactions, we have categorised our observations and created an overview map. The results demonstrate that detailed nanoscale resolution images are required to begin understanding the wide variety of individual cells’ interactions with a structured substrate. The map will provide a framework for light microscopy studies of such interactions indicating what modes of interactions must be considered. Public Library of Science 2013-01-09 /pmc/articles/PMC3541134/ /pubmed/23326412 http://dx.doi.org/10.1371/journal.pone.0053307 Text en © 2013 Wierzbicki et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wierzbicki, Rafał
Købler, Carsten
Jensen, Mikkel R. B.
Łopacińska, Joanna
Schmidt, Michael S.
Skolimowski, Maciej
Abeille, Fabien
Qvortrup, Klaus
Mølhave, Kristian
Mapping the Complex Morphology of Cell Interactions with Nanowire Substrates Using FIB-SEM
title Mapping the Complex Morphology of Cell Interactions with Nanowire Substrates Using FIB-SEM
title_full Mapping the Complex Morphology of Cell Interactions with Nanowire Substrates Using FIB-SEM
title_fullStr Mapping the Complex Morphology of Cell Interactions with Nanowire Substrates Using FIB-SEM
title_full_unstemmed Mapping the Complex Morphology of Cell Interactions with Nanowire Substrates Using FIB-SEM
title_short Mapping the Complex Morphology of Cell Interactions with Nanowire Substrates Using FIB-SEM
title_sort mapping the complex morphology of cell interactions with nanowire substrates using fib-sem
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3541134/
https://www.ncbi.nlm.nih.gov/pubmed/23326412
http://dx.doi.org/10.1371/journal.pone.0053307
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