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Retrograde Analysis of Calcium Signaling by CaMPARI2 Shows Cytosolic Calcium in Chondrocytes Is Unaffected by Parabolic Flights
Calcium (Ca(2+)) elevation is an essential secondary messenger in many cellular processes, including disease progression and adaptation to external stimuli, e.g., gravitational load. Therefore, mapping and quantifying Ca(2+) signaling with a high spatiotemporal resolution is a key challenge. However...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773224/ https://www.ncbi.nlm.nih.gov/pubmed/35052817 http://dx.doi.org/10.3390/biomedicines10010138 |
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author | Hammer, Andreas Cerretti, Geraldine Ricciardi, Dario A. Schiffmann, David Maranda, Simon Kummer, Raphael Zumbühl, Christoph Rattenbacher-Kiser, Karin F. von Arx, Silvan Ammann, Sebastian Strobl, Frederic Berkane, Rayene Stolz, Alexandra Stelzer, Ernst H. K. Egli, Marcel Schleiff, Enrico Wuest, Simon L. Böhmer, Maik |
author_facet | Hammer, Andreas Cerretti, Geraldine Ricciardi, Dario A. Schiffmann, David Maranda, Simon Kummer, Raphael Zumbühl, Christoph Rattenbacher-Kiser, Karin F. von Arx, Silvan Ammann, Sebastian Strobl, Frederic Berkane, Rayene Stolz, Alexandra Stelzer, Ernst H. K. Egli, Marcel Schleiff, Enrico Wuest, Simon L. Böhmer, Maik |
author_sort | Hammer, Andreas |
collection | PubMed |
description | Calcium (Ca(2+)) elevation is an essential secondary messenger in many cellular processes, including disease progression and adaptation to external stimuli, e.g., gravitational load. Therefore, mapping and quantifying Ca(2+) signaling with a high spatiotemporal resolution is a key challenge. However, particularly on microgravity platforms, experiment time is limited, allowing only a small number of replicates. Furthermore, experiment hardware is exposed to changes in gravity levels, causing experimental artifacts unless appropriately controlled. We introduce a new experimental setup based on the fluorescent Ca(2+) reporter CaMPARI2, onboard LED arrays, and subsequent microscopic analysis on the ground. This setup allows for higher throughput and accuracy due to its retrograde nature. The excellent performance of CaMPARI2 was demonstrated with human chondrocytes during the 75th ESA parabolic flight campaign. CaMPARI2 revealed a strong Ca(2+) response triggered by histamine but was not affected by the alternating gravitational load of a parabolic flight. |
format | Online Article Text |
id | pubmed-8773224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87732242022-01-21 Retrograde Analysis of Calcium Signaling by CaMPARI2 Shows Cytosolic Calcium in Chondrocytes Is Unaffected by Parabolic Flights Hammer, Andreas Cerretti, Geraldine Ricciardi, Dario A. Schiffmann, David Maranda, Simon Kummer, Raphael Zumbühl, Christoph Rattenbacher-Kiser, Karin F. von Arx, Silvan Ammann, Sebastian Strobl, Frederic Berkane, Rayene Stolz, Alexandra Stelzer, Ernst H. K. Egli, Marcel Schleiff, Enrico Wuest, Simon L. Böhmer, Maik Biomedicines Article Calcium (Ca(2+)) elevation is an essential secondary messenger in many cellular processes, including disease progression and adaptation to external stimuli, e.g., gravitational load. Therefore, mapping and quantifying Ca(2+) signaling with a high spatiotemporal resolution is a key challenge. However, particularly on microgravity platforms, experiment time is limited, allowing only a small number of replicates. Furthermore, experiment hardware is exposed to changes in gravity levels, causing experimental artifacts unless appropriately controlled. We introduce a new experimental setup based on the fluorescent Ca(2+) reporter CaMPARI2, onboard LED arrays, and subsequent microscopic analysis on the ground. This setup allows for higher throughput and accuracy due to its retrograde nature. The excellent performance of CaMPARI2 was demonstrated with human chondrocytes during the 75th ESA parabolic flight campaign. CaMPARI2 revealed a strong Ca(2+) response triggered by histamine but was not affected by the alternating gravitational load of a parabolic flight. MDPI 2022-01-08 /pmc/articles/PMC8773224/ /pubmed/35052817 http://dx.doi.org/10.3390/biomedicines10010138 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hammer, Andreas Cerretti, Geraldine Ricciardi, Dario A. Schiffmann, David Maranda, Simon Kummer, Raphael Zumbühl, Christoph Rattenbacher-Kiser, Karin F. von Arx, Silvan Ammann, Sebastian Strobl, Frederic Berkane, Rayene Stolz, Alexandra Stelzer, Ernst H. K. Egli, Marcel Schleiff, Enrico Wuest, Simon L. Böhmer, Maik Retrograde Analysis of Calcium Signaling by CaMPARI2 Shows Cytosolic Calcium in Chondrocytes Is Unaffected by Parabolic Flights |
title | Retrograde Analysis of Calcium Signaling by CaMPARI2 Shows Cytosolic Calcium in Chondrocytes Is Unaffected by Parabolic Flights |
title_full | Retrograde Analysis of Calcium Signaling by CaMPARI2 Shows Cytosolic Calcium in Chondrocytes Is Unaffected by Parabolic Flights |
title_fullStr | Retrograde Analysis of Calcium Signaling by CaMPARI2 Shows Cytosolic Calcium in Chondrocytes Is Unaffected by Parabolic Flights |
title_full_unstemmed | Retrograde Analysis of Calcium Signaling by CaMPARI2 Shows Cytosolic Calcium in Chondrocytes Is Unaffected by Parabolic Flights |
title_short | Retrograde Analysis of Calcium Signaling by CaMPARI2 Shows Cytosolic Calcium in Chondrocytes Is Unaffected by Parabolic Flights |
title_sort | retrograde analysis of calcium signaling by campari2 shows cytosolic calcium in chondrocytes is unaffected by parabolic flights |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773224/ https://www.ncbi.nlm.nih.gov/pubmed/35052817 http://dx.doi.org/10.3390/biomedicines10010138 |
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