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Red Blood Cell Passage of Small Capillaries Is Associated with Transient Ca(2+)-mediated Adaptations
When red blood cells (RBCs) pass constrictions or small capillaries they need to pass apertures falling well below their own cross section size. We used different means of mechanical stimulations (hypoosmotic swelling, local mechanical stimulation, passing through microfluidic constrictions) to obse...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723316/ https://www.ncbi.nlm.nih.gov/pubmed/29259557 http://dx.doi.org/10.3389/fphys.2017.00979 |
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author | Danielczok, Jens G. Terriac, Emmanuel Hertz, Laura Petkova-Kirova, Polina Lautenschläger, Franziska Laschke, Matthias W. Kaestner, Lars |
author_facet | Danielczok, Jens G. Terriac, Emmanuel Hertz, Laura Petkova-Kirova, Polina Lautenschläger, Franziska Laschke, Matthias W. Kaestner, Lars |
author_sort | Danielczok, Jens G. |
collection | PubMed |
description | When red blood cells (RBCs) pass constrictions or small capillaries they need to pass apertures falling well below their own cross section size. We used different means of mechanical stimulations (hypoosmotic swelling, local mechanical stimulation, passing through microfluidic constrictions) to observe cellular responses of human RBCs in terms of intracellular Ca(2+)-signaling by confocal microscopy of Fluo-4 loaded RBCs. We were able to confirm our in vitro results in a mouse dorsal skinfold chamber model showing a transiently increased intracellular Ca(2+) when RBCs were passing through small capillaries in vivo. Furthermore, we performed the above-mentioned in vitro experiments as well as measurements of RBCs filterability under various pharmacological manipulations (GsMTx-4, TRAM-34) to explore the molecular mechanism of the Ca(2+)-signaling. Based on these experiments we conclude that mechanical stimulation of RBCs activates mechano-sensitive channels most likely Piezo1. This channel activity allows Ca(2+) to enter the cell, leading to a transient activation of the Gardos-channel associated with K(+), Cl(−), and water loss, i.e., with a transient volume adaptation facilitating the passage of the RBCs through the constriction. |
format | Online Article Text |
id | pubmed-5723316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57233162017-12-19 Red Blood Cell Passage of Small Capillaries Is Associated with Transient Ca(2+)-mediated Adaptations Danielczok, Jens G. Terriac, Emmanuel Hertz, Laura Petkova-Kirova, Polina Lautenschläger, Franziska Laschke, Matthias W. Kaestner, Lars Front Physiol Physiology When red blood cells (RBCs) pass constrictions or small capillaries they need to pass apertures falling well below their own cross section size. We used different means of mechanical stimulations (hypoosmotic swelling, local mechanical stimulation, passing through microfluidic constrictions) to observe cellular responses of human RBCs in terms of intracellular Ca(2+)-signaling by confocal microscopy of Fluo-4 loaded RBCs. We were able to confirm our in vitro results in a mouse dorsal skinfold chamber model showing a transiently increased intracellular Ca(2+) when RBCs were passing through small capillaries in vivo. Furthermore, we performed the above-mentioned in vitro experiments as well as measurements of RBCs filterability under various pharmacological manipulations (GsMTx-4, TRAM-34) to explore the molecular mechanism of the Ca(2+)-signaling. Based on these experiments we conclude that mechanical stimulation of RBCs activates mechano-sensitive channels most likely Piezo1. This channel activity allows Ca(2+) to enter the cell, leading to a transient activation of the Gardos-channel associated with K(+), Cl(−), and water loss, i.e., with a transient volume adaptation facilitating the passage of the RBCs through the constriction. Frontiers Media S.A. 2017-12-05 /pmc/articles/PMC5723316/ /pubmed/29259557 http://dx.doi.org/10.3389/fphys.2017.00979 Text en Copyright © 2017 Danielczok, Terriac, Hertz, Petkova-Kirova, Lautenschläger, Laschke and Kaestner. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Danielczok, Jens G. Terriac, Emmanuel Hertz, Laura Petkova-Kirova, Polina Lautenschläger, Franziska Laschke, Matthias W. Kaestner, Lars Red Blood Cell Passage of Small Capillaries Is Associated with Transient Ca(2+)-mediated Adaptations |
title | Red Blood Cell Passage of Small Capillaries Is Associated with Transient Ca(2+)-mediated Adaptations |
title_full | Red Blood Cell Passage of Small Capillaries Is Associated with Transient Ca(2+)-mediated Adaptations |
title_fullStr | Red Blood Cell Passage of Small Capillaries Is Associated with Transient Ca(2+)-mediated Adaptations |
title_full_unstemmed | Red Blood Cell Passage of Small Capillaries Is Associated with Transient Ca(2+)-mediated Adaptations |
title_short | Red Blood Cell Passage of Small Capillaries Is Associated with Transient Ca(2+)-mediated Adaptations |
title_sort | red blood cell passage of small capillaries is associated with transient ca(2+)-mediated adaptations |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723316/ https://www.ncbi.nlm.nih.gov/pubmed/29259557 http://dx.doi.org/10.3389/fphys.2017.00979 |
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