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Massachusetts Institute of Technology

Stochastic modeling of intracellular signaling dynamics for the purpose of regulating endothelial cell migration

Abstract

dc:description.abstract

Effective control of cellular behaviors has serious implications in the study of biological processes and disease. However, phenotypic changes may be difficult to detect instantaneously and are usually associated with noticeable delay between input cue and output cellular response. Because of this, relying on detection of phenotypic behaviors for use in feedback control may lead to instability and decreased controller performance. In order to alleviate these issues, a new approach to regulating cell behaviors through control of intracellular signaling events is presented. Many cell behaviors are mediated by a network of intracellular protein activations that originate at the membrane in response to stimulation of cell surface receptors. Multiple protein signaling transductions occur concurrently through diverse pathways triggered by different extracellular cues. Cell behavior differs, depending on the chronological order of multiple signaling events. This thesis develops several modeling frameworks for an intracellular signaling network specific to endothelial cell migration in angiogenesis. Unlike previous works, the models developed in this thesis exploit the effect of signaling order on extracellular response. Our approach examines the transduction time associated with each pathway of a cascaded signaling network. Transduction times of multiple pathways are compared, and the probability that the multiple signaling events occur in a desired chronological order is evaluated. We begin our development with an input-output time-delay model derived from simulated data that is used to predict the optimal extracellular input intensity for a desired response. We then present a stochastic "pseudo-discrete" model of the signal transduction time. We conclude by presenting several control strategies for control of intracellular signaling events.

Degree

thesis:*
Department dc:contributor.department
Massachusetts Institute of Technology. Dept. of Mechanical Engineering.
Grantor dc:publisher
Massachusetts Institute of Technology
Year dc:date.issued
2012

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Mayalu, Michaëlle Ntala
Advisor dc:contributor.advisor
  • H. Harry Asada.

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.
Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/1721.1/74929
OAI identifier oai:identifier
oai:dspace.mit.edu:1721.1/74929

Chain of custody

source
Harvested from
MIT
Base URL
dspace.mit.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Mayalu, Michaëlle Ntala. Stochastic modeling of intracellular signaling dynamics for the purpose of regulating endothelial cell migration. Massachusetts Institute of Technology, 2012. http://hdl.handle.net/1721.1/74929