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Time resolved 3D live-cell imaging on implants

It is estimated that two million new dental implants are inserted worldwide each year. Innovative implant materials are developed in order to minimize the risk of peri-implant inflammations. The broad range of material testing is conducted using standard 2D, terminal, and invasive methods. The metho...

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Autores principales: Ingendoh-Tsakmakidis, Alexandra, Nolte, Lena, Winkel, Andreas, Meyer, Heiko, Koroleva, Anastasia, Shpichka, Anastasia, Ripken, Tammo, Heisterkamp, Alexander, Stiesch, Meike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6179276/
https://www.ncbi.nlm.nih.gov/pubmed/30304039
http://dx.doi.org/10.1371/journal.pone.0205411
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author Ingendoh-Tsakmakidis, Alexandra
Nolte, Lena
Winkel, Andreas
Meyer, Heiko
Koroleva, Anastasia
Shpichka, Anastasia
Ripken, Tammo
Heisterkamp, Alexander
Stiesch, Meike
author_facet Ingendoh-Tsakmakidis, Alexandra
Nolte, Lena
Winkel, Andreas
Meyer, Heiko
Koroleva, Anastasia
Shpichka, Anastasia
Ripken, Tammo
Heisterkamp, Alexander
Stiesch, Meike
author_sort Ingendoh-Tsakmakidis, Alexandra
collection PubMed
description It is estimated that two million new dental implants are inserted worldwide each year. Innovative implant materials are developed in order to minimize the risk of peri-implant inflammations. The broad range of material testing is conducted using standard 2D, terminal, and invasive methods. The methods that have been applied are not sufficient to monitor the whole implant surface and temporal progress. Therefore, we built a 3D peri-implant model using a cylindrical implant colonized by human gingival fibroblasts. In order to monitor the cell response over time, a non-toxic LIVE/DEAD staining was established and applied to the new 3D model. Our LIVE/DEAD staining method in combination with the time resolved 3D visualization using Scanning Laser Optical Tomography (SLOT), allowed us to monitor the cell death path along the implant in the 3D peri-implant model. The differentiation of living and dead gingival fibroblasts in response to toxicity was effectively supported by the LIVE/DEAD staining. Furthermore, it was possible to visualize the whole cell-colonized implant in 3D and up to 63 hours. This new methodology offers the opportunity to record the long-term cell response on external stress factors, along the dental implant and thus to evaluate the performance of novel materials/surfaces.
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spelling pubmed-61792762018-10-26 Time resolved 3D live-cell imaging on implants Ingendoh-Tsakmakidis, Alexandra Nolte, Lena Winkel, Andreas Meyer, Heiko Koroleva, Anastasia Shpichka, Anastasia Ripken, Tammo Heisterkamp, Alexander Stiesch, Meike PLoS One Research Article It is estimated that two million new dental implants are inserted worldwide each year. Innovative implant materials are developed in order to minimize the risk of peri-implant inflammations. The broad range of material testing is conducted using standard 2D, terminal, and invasive methods. The methods that have been applied are not sufficient to monitor the whole implant surface and temporal progress. Therefore, we built a 3D peri-implant model using a cylindrical implant colonized by human gingival fibroblasts. In order to monitor the cell response over time, a non-toxic LIVE/DEAD staining was established and applied to the new 3D model. Our LIVE/DEAD staining method in combination with the time resolved 3D visualization using Scanning Laser Optical Tomography (SLOT), allowed us to monitor the cell death path along the implant in the 3D peri-implant model. The differentiation of living and dead gingival fibroblasts in response to toxicity was effectively supported by the LIVE/DEAD staining. Furthermore, it was possible to visualize the whole cell-colonized implant in 3D and up to 63 hours. This new methodology offers the opportunity to record the long-term cell response on external stress factors, along the dental implant and thus to evaluate the performance of novel materials/surfaces. Public Library of Science 2018-10-10 /pmc/articles/PMC6179276/ /pubmed/30304039 http://dx.doi.org/10.1371/journal.pone.0205411 Text en © 2018 Ingendoh-Tsakmakidis 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ingendoh-Tsakmakidis, Alexandra
Nolte, Lena
Winkel, Andreas
Meyer, Heiko
Koroleva, Anastasia
Shpichka, Anastasia
Ripken, Tammo
Heisterkamp, Alexander
Stiesch, Meike
Time resolved 3D live-cell imaging on implants
title Time resolved 3D live-cell imaging on implants
title_full Time resolved 3D live-cell imaging on implants
title_fullStr Time resolved 3D live-cell imaging on implants
title_full_unstemmed Time resolved 3D live-cell imaging on implants
title_short Time resolved 3D live-cell imaging on implants
title_sort time resolved 3d live-cell imaging on implants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6179276/
https://www.ncbi.nlm.nih.gov/pubmed/30304039
http://dx.doi.org/10.1371/journal.pone.0205411
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