Cargando…
Intracellular calcium signals display an avalanche-like behavior over multiple lengthscales
Many natural phenomena display “self-organized criticality” (SOC), (Bak et al., 1987). This refers to spatially extended systems for which patterns of activity characterized by different lengthscales can occur with a probability density that follows a power law with pattern size. Differently from po...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432517/ https://www.ncbi.nlm.nih.gov/pubmed/22969730 http://dx.doi.org/10.3389/fphys.2012.00350 |
_version_ | 1782242218190307328 |
---|---|
author | Lopez, Lucía Piegari, Estefanía Sigaut, Lorena Ponce Dawson, Silvina |
author_facet | Lopez, Lucía Piegari, Estefanía Sigaut, Lorena Ponce Dawson, Silvina |
author_sort | Lopez, Lucía |
collection | PubMed |
description | Many natural phenomena display “self-organized criticality” (SOC), (Bak et al., 1987). This refers to spatially extended systems for which patterns of activity characterized by different lengthscales can occur with a probability density that follows a power law with pattern size. Differently from power laws at phase transitions, systems displaying SOC do not need the tuning of an external parameter. Here we analyze intracellular calcium (Ca(2+)) signals, a key component of the signaling toolkit of almost any cell type. Ca(2+) signals can either be spatially restricted (local) or propagate throughout the cell (global). Different models have suggested that the transition from local to global signals is similar to that of directed percolation. Directed percolation has been associated, in turn, to the appearance of SOC. In this paper we discuss these issues within the framework of simple models of Ca(2+) signal propagation. We also analyze the size distribution of local signals (“puffs”) observed in immature Xenopus Laevis oocytes. The puff amplitude distribution obtained from observed local signals is not Gaussian with a noticeable fraction of large size events. The experimental distribution of puff areas in the spatio-temporal record of the image has a long tail that is approximately log-normal. The distribution can also be fitted with a power law relationship albeit with a smaller goodness of fit. The power law behavior is encountered within a simple model that includes some coupling among individual signals for a wide range of parameter values. An analysis of the model shows that a global elevation of the Ca(2+) concentration plays a major role in determining whether the puff size distribution is long-tailed or not. This suggests that Ca(2+)-clearing from the cytosol is key to determine whether IP(3)-mediated Ca(2+) signals can display a SOC-like behavior or not. |
format | Online Article Text |
id | pubmed-3432517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-34325172012-09-11 Intracellular calcium signals display an avalanche-like behavior over multiple lengthscales Lopez, Lucía Piegari, Estefanía Sigaut, Lorena Ponce Dawson, Silvina Front Physiol Physiology Many natural phenomena display “self-organized criticality” (SOC), (Bak et al., 1987). This refers to spatially extended systems for which patterns of activity characterized by different lengthscales can occur with a probability density that follows a power law with pattern size. Differently from power laws at phase transitions, systems displaying SOC do not need the tuning of an external parameter. Here we analyze intracellular calcium (Ca(2+)) signals, a key component of the signaling toolkit of almost any cell type. Ca(2+) signals can either be spatially restricted (local) or propagate throughout the cell (global). Different models have suggested that the transition from local to global signals is similar to that of directed percolation. Directed percolation has been associated, in turn, to the appearance of SOC. In this paper we discuss these issues within the framework of simple models of Ca(2+) signal propagation. We also analyze the size distribution of local signals (“puffs”) observed in immature Xenopus Laevis oocytes. The puff amplitude distribution obtained from observed local signals is not Gaussian with a noticeable fraction of large size events. The experimental distribution of puff areas in the spatio-temporal record of the image has a long tail that is approximately log-normal. The distribution can also be fitted with a power law relationship albeit with a smaller goodness of fit. The power law behavior is encountered within a simple model that includes some coupling among individual signals for a wide range of parameter values. An analysis of the model shows that a global elevation of the Ca(2+) concentration plays a major role in determining whether the puff size distribution is long-tailed or not. This suggests that Ca(2+)-clearing from the cytosol is key to determine whether IP(3)-mediated Ca(2+) signals can display a SOC-like behavior or not. Frontiers Media S.A. 2012-09-03 /pmc/articles/PMC3432517/ /pubmed/22969730 http://dx.doi.org/10.3389/fphys.2012.00350 Text en Copyright © 2012 Lopez, Piegari, Sigaut and Ponce Dawson. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Physiology Lopez, Lucía Piegari, Estefanía Sigaut, Lorena Ponce Dawson, Silvina Intracellular calcium signals display an avalanche-like behavior over multiple lengthscales |
title | Intracellular calcium signals display an avalanche-like behavior over multiple lengthscales |
title_full | Intracellular calcium signals display an avalanche-like behavior over multiple lengthscales |
title_fullStr | Intracellular calcium signals display an avalanche-like behavior over multiple lengthscales |
title_full_unstemmed | Intracellular calcium signals display an avalanche-like behavior over multiple lengthscales |
title_short | Intracellular calcium signals display an avalanche-like behavior over multiple lengthscales |
title_sort | intracellular calcium signals display an avalanche-like behavior over multiple lengthscales |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432517/ https://www.ncbi.nlm.nih.gov/pubmed/22969730 http://dx.doi.org/10.3389/fphys.2012.00350 |
work_keys_str_mv | AT lopezlucia intracellularcalciumsignalsdisplayanavalanchelikebehaviorovermultiplelengthscales AT piegariestefania intracellularcalciumsignalsdisplayanavalanchelikebehaviorovermultiplelengthscales AT sigautlorena intracellularcalciumsignalsdisplayanavalanchelikebehaviorovermultiplelengthscales AT poncedawsonsilvina intracellularcalciumsignalsdisplayanavalanchelikebehaviorovermultiplelengthscales |