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Cytoplasmic convection currents and intracellular temperature gradients
Intracellular thermometry has recently demonstrated temperatures in the nucleus, mitochondria, and centrosome to be significantly higher than those of the cytoplasm and cell membrane. This local thermogenesis and the resulting temperature gradient could facilitate the development of persistent, self...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827888/ https://www.ncbi.nlm.nih.gov/pubmed/31682599 http://dx.doi.org/10.1371/journal.pcbi.1007372 |
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author | Howard, Rachel Scheiner, Aaron Cunningham, Jessica Gatenby, Robert |
author_facet | Howard, Rachel Scheiner, Aaron Cunningham, Jessica Gatenby, Robert |
author_sort | Howard, Rachel |
collection | PubMed |
description | Intracellular thermometry has recently demonstrated temperatures in the nucleus, mitochondria, and centrosome to be significantly higher than those of the cytoplasm and cell membrane. This local thermogenesis and the resulting temperature gradient could facilitate the development of persistent, self-organizing convection currents in the cytoplasm of large eukaryotes. Using 3-dimensional computational simulations of intracellular fluid motion, we quantify the convective velocities that could result from the temperature differences observed experimentally. Based on these velocities, we identify the conditions necessary for this temperature-driven bulk flow to dominate over random thermal diffusive motion at the scale of a single eukaryotic cell. With temperature gradients of the order 1°C and diffusion coefficients comparable to those described in the literature, Péclet numbers ≥ 1 are feasible and permit comparable or greater effects of convection than diffusion in determining intracellular mass flux. In addition to the temperature gradient, the resulting flow patterns would also depend on the spatial localization of the heat source, the shape of the cell membrane, and the complex intracellular structure including the cytoskeleton. While this intracellular convection would be highly context-dependent, in certain settings, convective motion could provide a previously unrecognized mechanism for directed, bulk transport within eukaryotic cells. |
format | Online Article Text |
id | pubmed-6827888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-68278882019-11-12 Cytoplasmic convection currents and intracellular temperature gradients Howard, Rachel Scheiner, Aaron Cunningham, Jessica Gatenby, Robert PLoS Comput Biol Research Article Intracellular thermometry has recently demonstrated temperatures in the nucleus, mitochondria, and centrosome to be significantly higher than those of the cytoplasm and cell membrane. This local thermogenesis and the resulting temperature gradient could facilitate the development of persistent, self-organizing convection currents in the cytoplasm of large eukaryotes. Using 3-dimensional computational simulations of intracellular fluid motion, we quantify the convective velocities that could result from the temperature differences observed experimentally. Based on these velocities, we identify the conditions necessary for this temperature-driven bulk flow to dominate over random thermal diffusive motion at the scale of a single eukaryotic cell. With temperature gradients of the order 1°C and diffusion coefficients comparable to those described in the literature, Péclet numbers ≥ 1 are feasible and permit comparable or greater effects of convection than diffusion in determining intracellular mass flux. In addition to the temperature gradient, the resulting flow patterns would also depend on the spatial localization of the heat source, the shape of the cell membrane, and the complex intracellular structure including the cytoskeleton. While this intracellular convection would be highly context-dependent, in certain settings, convective motion could provide a previously unrecognized mechanism for directed, bulk transport within eukaryotic cells. Public Library of Science 2019-11-04 /pmc/articles/PMC6827888/ /pubmed/31682599 http://dx.doi.org/10.1371/journal.pcbi.1007372 Text en © 2019 Howard 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 Howard, Rachel Scheiner, Aaron Cunningham, Jessica Gatenby, Robert Cytoplasmic convection currents and intracellular temperature gradients |
title | Cytoplasmic convection currents and intracellular temperature gradients |
title_full | Cytoplasmic convection currents and intracellular temperature gradients |
title_fullStr | Cytoplasmic convection currents and intracellular temperature gradients |
title_full_unstemmed | Cytoplasmic convection currents and intracellular temperature gradients |
title_short | Cytoplasmic convection currents and intracellular temperature gradients |
title_sort | cytoplasmic convection currents and intracellular temperature gradients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827888/ https://www.ncbi.nlm.nih.gov/pubmed/31682599 http://dx.doi.org/10.1371/journal.pcbi.1007372 |
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