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Divergent calcium signaling in RBCs from Tropidurus torquatus (Squamata – Tropiduridae) strengthen classification in lizard evolution
BACKGROUND: We have previously reported that a Teiid lizard red blood cells (RBCs) such as Ameiva ameiva and Tupinambis merianae controls intracellular calcium levels by displaying multiple mechanisms. In these cells, calcium stores could be discharged not only by: thapsigargin, but also by the Na(+...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2018699/ https://www.ncbi.nlm.nih.gov/pubmed/17716375 http://dx.doi.org/10.1186/1472-6793-7-7 |
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author | Beraldo, Flávio H Garcia, Célia RS |
author_facet | Beraldo, Flávio H Garcia, Célia RS |
author_sort | Beraldo, Flávio H |
collection | PubMed |
description | BACKGROUND: We have previously reported that a Teiid lizard red blood cells (RBCs) such as Ameiva ameiva and Tupinambis merianae controls intracellular calcium levels by displaying multiple mechanisms. In these cells, calcium stores could be discharged not only by: thapsigargin, but also by the Na(+)/H(+ )ionophore monensin, K(+)/H(+ )ionophore nigericin and the H(+ )pump inhibitor bafilomycin as well as ionomycin. Moreover, these lizards possess a P2Y-type purinoceptors that mobilize Ca(2+ )from intracellular stores upon ATP addition. RESULTS: Here we report, that RBCs from the tropidurid lizard Tropidurus torquatus store Ca(2+ )in endoplasmic reticulum (ER) pool but unlike in the referred Teiidae, these cells do not store calcium in monensin-nigericin sensitive pools. Moreover, mitochondria from T. torquatus RBCs accumulate Ca(2+). Addition of ATP to a calcium-free medium does not increase the [Ca(2+)](c )levels, however in a calcium medium we observe an increase in cytosolic calcium. This is an indication that purinergic receptors in these cells are P2X-like. CONCLUSION: T. torquatus RBCs present different mechanisms from Teiid lizard red blood cells (RBCs), for controlling its intracellular calcium levels. At T. torquatus the ion is only stored at endoplasmic reticulum and mitochondria. Moreover activation of purinergic receptor, P2X type, was able to induce an influx of calcium from extracelullar medium. These studies contribute to the understanding of the evolution of calcium homeostasis and signaling in nucleated RBCs. |
format | Text |
id | pubmed-2018699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-20186992007-10-12 Divergent calcium signaling in RBCs from Tropidurus torquatus (Squamata – Tropiduridae) strengthen classification in lizard evolution Beraldo, Flávio H Garcia, Célia RS BMC Physiol Research Article BACKGROUND: We have previously reported that a Teiid lizard red blood cells (RBCs) such as Ameiva ameiva and Tupinambis merianae controls intracellular calcium levels by displaying multiple mechanisms. In these cells, calcium stores could be discharged not only by: thapsigargin, but also by the Na(+)/H(+ )ionophore monensin, K(+)/H(+ )ionophore nigericin and the H(+ )pump inhibitor bafilomycin as well as ionomycin. Moreover, these lizards possess a P2Y-type purinoceptors that mobilize Ca(2+ )from intracellular stores upon ATP addition. RESULTS: Here we report, that RBCs from the tropidurid lizard Tropidurus torquatus store Ca(2+ )in endoplasmic reticulum (ER) pool but unlike in the referred Teiidae, these cells do not store calcium in monensin-nigericin sensitive pools. Moreover, mitochondria from T. torquatus RBCs accumulate Ca(2+). Addition of ATP to a calcium-free medium does not increase the [Ca(2+)](c )levels, however in a calcium medium we observe an increase in cytosolic calcium. This is an indication that purinergic receptors in these cells are P2X-like. CONCLUSION: T. torquatus RBCs present different mechanisms from Teiid lizard red blood cells (RBCs), for controlling its intracellular calcium levels. At T. torquatus the ion is only stored at endoplasmic reticulum and mitochondria. Moreover activation of purinergic receptor, P2X type, was able to induce an influx of calcium from extracelullar medium. These studies contribute to the understanding of the evolution of calcium homeostasis and signaling in nucleated RBCs. BioMed Central 2007-08-23 /pmc/articles/PMC2018699/ /pubmed/17716375 http://dx.doi.org/10.1186/1472-6793-7-7 Text en Copyright © 2007 Beraldo and Garcia; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Beraldo, Flávio H Garcia, Célia RS Divergent calcium signaling in RBCs from Tropidurus torquatus (Squamata – Tropiduridae) strengthen classification in lizard evolution |
title | Divergent calcium signaling in RBCs from Tropidurus torquatus (Squamata – Tropiduridae) strengthen classification in lizard evolution |
title_full | Divergent calcium signaling in RBCs from Tropidurus torquatus (Squamata – Tropiduridae) strengthen classification in lizard evolution |
title_fullStr | Divergent calcium signaling in RBCs from Tropidurus torquatus (Squamata – Tropiduridae) strengthen classification in lizard evolution |
title_full_unstemmed | Divergent calcium signaling in RBCs from Tropidurus torquatus (Squamata – Tropiduridae) strengthen classification in lizard evolution |
title_short | Divergent calcium signaling in RBCs from Tropidurus torquatus (Squamata – Tropiduridae) strengthen classification in lizard evolution |
title_sort | divergent calcium signaling in rbcs from tropidurus torquatus (squamata – tropiduridae) strengthen classification in lizard evolution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2018699/ https://www.ncbi.nlm.nih.gov/pubmed/17716375 http://dx.doi.org/10.1186/1472-6793-7-7 |
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