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Title:Assessing different temporal scales of calcium dynamics in networks of beta cell populations
Authors:ID Zmazek, Jan (Author)
ID Skelin, Maša (Author)
ID Markovič, Rene (Author)
ID Dolenšek, Jurij (Author)
ID Marhl, Marko (Author)
ID Stožer, Andraž (Author)
ID Gosak, Marko (Author)
Files:.pdf RAZ_Zmazek_Jan_2021.pdf (9,40 MB)
MD5: E1468A47227F021064C46CF0C9D6E9CC
 
URL https://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2021.612233/full
 
Language:English
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FNM - Faculty of Natural Sciences and Mathematics
MF - Faculty of Medicine
FERI - Faculty of Electrical Engineering and Computer Science
PEF - Faculty of Education
Abstract:Beta cells within the pancreatic islets of Langerhans respond to stimulation with coherent oscillations of membrane potential and intracellular calcium concentration that presumably drive the pulsatile exocytosis of insulin. Their rhythmic activity is multimodal, resulting from networked feedback interactions of various oscillatory subsystems, such as the glycolytic, mitochondrial, and electrical/calcium components.How these oscillatory modules interact and affect the collective cellular activity, which is a prerequisite for proper hormone release, is incompletely understood. In the present work, we combined advanced confocal Ca2+ imaging in fresh mouse pancreas tissue slices with time series analysis and network science approaches to unveil the glucosedependent characteristics of different oscillatory components on both the intra- and inter-cellular level. Our results reveal an interrelationship between the metabolically driven low-frequency component and the electrically driven high-frequency component, with the latter exhibiting the highest bursting rates around the peaks of the slow component and the lowest around the nadirs. Moreover, the activity, as well as the average synchronicity of the fast component, considerably increased with increasing stimulatory glucose concentration, whereas the stimulation level did not affect any of these parameters in the slow component domain. Remarkably, in both dynamical components, the average correlation decreased similarly with intercellular distance, which implies that intercellular communication affects the synchronicity of both types of oscillations. To explore the intra-islet synchronization patterns in more detail, we constructed functional connectivity maps. The subsequent comparison of network characteristics of different oscillatory components showed more locally clustered and segregated networks of fast oscillatory activity, while the slow oscillations were more global, resulting in several long-range connections and a more cohesive structure. Besides the structural differences, we found a relatively weak relationship between the fast and slow network layer, which suggests that different synchronization mechanisms shape the collective cellular activity in islets, a finding which has to be kept in mind in future studies employing different oscillations for constructing networks.
Keywords:islets of Langerhans, beta cell network, calcium oscillations, multimodal activity analysis, confocal imaging, functional connectivity, multiplex network
Publication status:Published
Publication version:Version of Record
Submitted for review:30.09.2020
Article acceptance date:26.02.2021
Publication date:23.03.2021
Year of publishing:2021
Number of pages:16 str.
Numbering:Vol. 12
PID:20.500.12556/DKUM-89004 New window
UDC:612.349.7
ISSN on article:1664-042X
COBISS.SI-ID:56986115 New window
DOI:10.3389/fphys.2021.612233 New window
Publication date in DKUM:06.06.2024
Views:171
Downloads:6
Metadata:XML DC-XML DC-RDF
Categories:Misc.
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Record is a part of a journal

Title:Frontiers in physiology
Shortened title:Front. physiol.
Publisher:Frontiers Research Foundation
ISSN:1664-042X
COBISS.SI-ID:1218939 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0396-2019
Name:Celične in tkivne mreže

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P1-0055-2015
Name:Biofizika polimerov, membran, gelov, koloidov in celic

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:I0-0029-2015
Name:Infrastrukturna dejavnost Univerze v Mariboru

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J3-9289-2018
Name:Vloga cikličnega adenozin monofosfata v normalni fiziologiji celic beta in med razvojem sladkorne bolezni tipa 2

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:N3-0048-2016
Name:Vloga ionskih kanalov TRPM3 in TRPM5 pri uravnavanju mrežne aktivnosti v otočkih trebušne slinavke

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:N3-0133-2020
Name:Celice beta med razvojem in remisijo z dieto povzročene sladkorne bolezni

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