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Random Matrix Analysis of Ca(2+) Signals in β-Cell Collectives

Even within small organs like pancreatic islets, different endocrine cell types and subtypes form a heterogeneous collective to sense the chemical composition of the extracellular solution and compute an adequate hormonal output. Erroneous cellular processing and hormonal output due to challenged he...

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Detalles Bibliográficos
Autores principales: Korošak, Dean, Slak Rupnik, Marjan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759485/
https://www.ncbi.nlm.nih.gov/pubmed/31620017
http://dx.doi.org/10.3389/fphys.2019.01194
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author Korošak, Dean
Slak Rupnik, Marjan
author_facet Korošak, Dean
Slak Rupnik, Marjan
author_sort Korošak, Dean
collection PubMed
description Even within small organs like pancreatic islets, different endocrine cell types and subtypes form a heterogeneous collective to sense the chemical composition of the extracellular solution and compute an adequate hormonal output. Erroneous cellular processing and hormonal output due to challenged heterogeneity result in various disorders with diabetes mellitus as a flagship metabolic disease. Here we attempt to address the aforementioned functional heterogeneity with comparing pairwise cell-cell cross-correlations obtained from simultaneous measurements of cytosolic calcium responses in hundreds of islet cells in an optical plane to statistical properties of correlations predicted by the random matrix theory (RMT). We find that the bulk of the empirical eigenvalue spectrum is almost completely described by RMT prediction, however, the deviating eigenvalues that exist below and above RMT spectral edges suggest that there are local and extended modes driving the correlations. We also show that empirical nearest neighbor spacing of eigenvalues follows universal RMT properties regardless of glucose stimulation, but that number variance displays clear separation from RMT prediction and can differentiate between empirical spectra obtained under non-stimulated and stimulated conditions. We suggest that RMT approach provides a sensitive tool to assess the functional cell heterogeneity and its effects on the spatio-temporal dynamics of a collective of beta cells in pancreatic islets in physiological resting and stimulatory conditions, beyond the current limitations of molecular and cellular biology.
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spelling pubmed-67594852019-10-16 Random Matrix Analysis of Ca(2+) Signals in β-Cell Collectives Korošak, Dean Slak Rupnik, Marjan Front Physiol Physiology Even within small organs like pancreatic islets, different endocrine cell types and subtypes form a heterogeneous collective to sense the chemical composition of the extracellular solution and compute an adequate hormonal output. Erroneous cellular processing and hormonal output due to challenged heterogeneity result in various disorders with diabetes mellitus as a flagship metabolic disease. Here we attempt to address the aforementioned functional heterogeneity with comparing pairwise cell-cell cross-correlations obtained from simultaneous measurements of cytosolic calcium responses in hundreds of islet cells in an optical plane to statistical properties of correlations predicted by the random matrix theory (RMT). We find that the bulk of the empirical eigenvalue spectrum is almost completely described by RMT prediction, however, the deviating eigenvalues that exist below and above RMT spectral edges suggest that there are local and extended modes driving the correlations. We also show that empirical nearest neighbor spacing of eigenvalues follows universal RMT properties regardless of glucose stimulation, but that number variance displays clear separation from RMT prediction and can differentiate between empirical spectra obtained under non-stimulated and stimulated conditions. We suggest that RMT approach provides a sensitive tool to assess the functional cell heterogeneity and its effects on the spatio-temporal dynamics of a collective of beta cells in pancreatic islets in physiological resting and stimulatory conditions, beyond the current limitations of molecular and cellular biology. Frontiers Media S.A. 2019-09-18 /pmc/articles/PMC6759485/ /pubmed/31620017 http://dx.doi.org/10.3389/fphys.2019.01194 Text en Copyright © 2019 Korošak and Slak Rupnik. 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) and the copyright owner(s) 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
Korošak, Dean
Slak Rupnik, Marjan
Random Matrix Analysis of Ca(2+) Signals in β-Cell Collectives
title Random Matrix Analysis of Ca(2+) Signals in β-Cell Collectives
title_full Random Matrix Analysis of Ca(2+) Signals in β-Cell Collectives
title_fullStr Random Matrix Analysis of Ca(2+) Signals in β-Cell Collectives
title_full_unstemmed Random Matrix Analysis of Ca(2+) Signals in β-Cell Collectives
title_short Random Matrix Analysis of Ca(2+) Signals in β-Cell Collectives
title_sort random matrix analysis of ca(2+) signals in β-cell collectives
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759485/
https://www.ncbi.nlm.nih.gov/pubmed/31620017
http://dx.doi.org/10.3389/fphys.2019.01194
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