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Massachusetts Institute of Technology

Quantitative modeling and control of nascent sprout geometry in in vitro Angiogenesis

Abstract

dc:description.abstract

Nascent blood vessel growth in angiogenesis is a complex process involving cellular response to biochemical growth factors, degradation of the surrounding matrix, and coordinated migration of multiple endothelial cells up a growth factor gradient. Mechanistic understanding and quantitative modeling of the dominant dynamics involved in nascent vessel growth will enable new strategies for regulating vessel growth rate and geometry, and will have implications in controlling growth of complete vascular networks in many research areas, ranging from cancer treatment and wound healing to tissue engineering. In this thesis, we investigate the dynamics of nascent vessel growth in 3D microfluidic assays, formulate a quantitative process model based on our experimental characterization, and formulate a feedback approach to regulate growth. We begin by developing a new microfluidic assay consisting of a collagen gel scaffold with features to reduce assay-to-assay variability and increase experimental throughput. This high throughput assay reveals that there is an inverse relationship between nascent vessel elongation rate and diameter under diverse biochemical conditions. This finding is supported by immuno-fluorescent staining and biochemical inhibition studies, which give insight into the dominant mechanisms determining nascent vessel diameter. Based on our experimental characterization, we formulate a simple quantitative reaction-diffusion model that relates vessel diameter to elongation rate, and supports our understanding of the relevant dynamics. We conclude by formulating a model-based optimization approach for planning the optimal trajectory of elongation rate vs. time needed to obtain desired sprout geometry, and illustrate in simulation that model predictive feedback control can be used to correct for noise in the response of elongation rate to growth factor inputs.

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
  • Wood, Levi Benjamin
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/1721.1/70427
OAI identifier oai:identifier
oai:dspace.mit.edu:1721.1/70427

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

Wood, Levi Benjamin. Quantitative modeling and control of nascent sprout geometry in in vitro Angiogenesis. Massachusetts Institute of Technology, 2012. http://hdl.handle.net/1721.1/70427