Theoretical Investigation of Architecture-Dependent Calcium Signaling in Multicellular Network

Persistent Link:
http://hdl.handle.net/10150/333338
Title:
Theoretical Investigation of Architecture-Dependent Calcium Signaling in Multicellular Network
Author:
Long, Juexuan
Issue Date:
2014
Publisher:
The University of Arizona.
Rights:
Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
Embargo:
Release 13-Aug-2016
Abstract:
Calcium signal can be found in many types of cell. It has been treated as a life and death signal in cell-level for triggering life at fertilization, controlling the development and differentiation of cells into specialized types, mediating the subsequent activity, and finally affecting the cell death. In tissues, intercellular calcium wave is thought to serve as a long-range signaling, affected by the cell architecture. The aim of this thesis is to provide insight into the intercellular calcium waves in multicellular complex structures subjected to mechano- or chemical-stimuli. In the mechano-stimulated study, we combine the development of theoretical and experimental study of the propagation of calcium signals in multicellular structures composed of human endothelial cells. This analysis provides evidence for an effect of architecture on the propagation of calcium signals and the effect of single and dual stimulation on the multicellular structures. A simple model was established based on the calcium release/intake reaction and diffusion through gap junction from stimulated cell to the downstream cells. The simulation result shows similar results as what is shown in experiments. In the chemical-stimulated model, we studied computationally the interdependence between intracellular calcium and inositol-1,4,5-trisphosphate (IP₃) pathway and cell-cell communication via gap junction. We investigate the influence of the microenvironment of cells on the frequency of intracellular calcium oscillation. The simulation result shows that the oscillation frequency of an isolated cell is lower than that of a cell embedded in a cell-chain. This phenomenon is attributed to retrograde diffusion of calcium and IP₃ originating from a widening range of cells in the chain undergoing oscillations. It further demonstrates the important influence of microenvironment on the bio-signaling propagation.
Type:
text; Electronic Dissertation
Keywords:
multicellular; simulation; Materials Science & Engineering; calcium signal
Degree Name:
Ph.D.
Degree Level:
doctoral
Degree Program:
Graduate College; Materials Science & Engineering
Degree Grantor:
University of Arizona
Advisor:
Deymier, Pierre A.

Full metadata record

DC FieldValue Language
dc.language.isoen_USen
dc.titleTheoretical Investigation of Architecture-Dependent Calcium Signaling in Multicellular Networken_US
dc.creatorLong, Juexuanen_US
dc.contributor.authorLong, Juexuanen_US
dc.date.issued2014-
dc.publisherThe University of Arizona.en_US
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en_US
dc.description.releaseRelease 13-Aug-2016en_US
dc.description.abstractCalcium signal can be found in many types of cell. It has been treated as a life and death signal in cell-level for triggering life at fertilization, controlling the development and differentiation of cells into specialized types, mediating the subsequent activity, and finally affecting the cell death. In tissues, intercellular calcium wave is thought to serve as a long-range signaling, affected by the cell architecture. The aim of this thesis is to provide insight into the intercellular calcium waves in multicellular complex structures subjected to mechano- or chemical-stimuli. In the mechano-stimulated study, we combine the development of theoretical and experimental study of the propagation of calcium signals in multicellular structures composed of human endothelial cells. This analysis provides evidence for an effect of architecture on the propagation of calcium signals and the effect of single and dual stimulation on the multicellular structures. A simple model was established based on the calcium release/intake reaction and diffusion through gap junction from stimulated cell to the downstream cells. The simulation result shows similar results as what is shown in experiments. In the chemical-stimulated model, we studied computationally the interdependence between intracellular calcium and inositol-1,4,5-trisphosphate (IP₃) pathway and cell-cell communication via gap junction. We investigate the influence of the microenvironment of cells on the frequency of intracellular calcium oscillation. The simulation result shows that the oscillation frequency of an isolated cell is lower than that of a cell embedded in a cell-chain. This phenomenon is attributed to retrograde diffusion of calcium and IP₃ originating from a widening range of cells in the chain undergoing oscillations. It further demonstrates the important influence of microenvironment on the bio-signaling propagation.en_US
dc.typetexten
dc.typeElectronic Dissertationen
dc.subjectmulticellularen_US
dc.subjectsimulationen_US
dc.subjectMaterials Science & Engineeringen_US
dc.subjectcalcium signalen_US
thesis.degree.namePh.D.en_US
thesis.degree.leveldoctoralen_US
thesis.degree.disciplineGraduate Collegeen_US
thesis.degree.disciplineMaterials Science & Engineeringen_US
thesis.degree.grantorUniversity of Arizonaen_US
dc.contributor.advisorDeymier, Pierre A.en_US
dc.contributor.committeememberDeymier, Pierre A.en_US
dc.contributor.committeememberWong, Pak Kinen_US
dc.contributor.committeememberErdmann, Roberten_US
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