Fibronectin splice isoforms in wound healing and vascular development

Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Biology, 2002.

Bibliographic Details
Main Author: Burrows, Stephanie Yvonne, 1974-
Other Authors: Richard O. Hynes.
Format: Thesis
Language:eng
Published: Massachusetts Institute of Technology 2006
Subjects:
Online Access:http://hdl.handle.net/1721.1/29909
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author Burrows, Stephanie Yvonne, 1974-
author2 Richard O. Hynes.
author_facet Richard O. Hynes.
Burrows, Stephanie Yvonne, 1974-
author_sort Burrows, Stephanie Yvonne, 1974-
collection MIT
description Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Biology, 2002.
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spelling mit-1721.1/299092019-04-12T09:41:17Z Fibronectin splice isoforms in wound healing and vascular development Burrows, Stephanie Yvonne, 1974- Richard O. Hynes. Massachusetts Institute of Technology. Dept. of Biology. Massachusetts Institute of Technology. Dept. of Biology. Biology. Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Biology, 2002. Includes bibliographical references (leaves 173-186). Fibronectins are a large family of extracellular matrix proteins that regulate cell adhesion, migration, differentiation and survival. Different isoforms of fibronectin arise via alternative splicing of the transcript of a single gene. Although many of the general functions of fibronectins have been elucidated, few specific functions of the alternatively spliced isoforms have been described. Studies of the expression patterns of the splice isoforms show that these proteins are present at high levels during embryonic development. In adult animals, these isoforms are expressed around the perimeter of blood vessels and are induced in response to injury. We have developed an in vitro system using a set of bacterially expressed fibronectins and fibronectin-null cells to look at the functions of the alternatively spliced isoforms in wound healing and vascular development. Our results indicate that the bacterially expressed fibronectins are fully functional and promote a number of well-established fibronectin functions. Therefore, these fusion proteins should be useful for investigations of splice isoform specific functions. Our experiments with fibronectin-null cells show that fibronectin negatively regulates the expression of the differentiation marker a-smooth muscle actin which is expressed by myofibroblasts during wound healing and by peri-endothelial cells during blood vessel development. by Stephanie Yvonne Burrows. Ph.D. 2006-03-24T18:02:08Z 2006-03-24T18:02:08Z 2002 2002 Thesis http://hdl.handle.net/1721.1/29909 51641679 eng 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. http://dspace.mit.edu/handle/1721.1/7582 186 leaves 6164407 bytes 6164212 bytes application/pdf application/pdf application/pdf Massachusetts Institute of Technology
spellingShingle Biology.
Burrows, Stephanie Yvonne, 1974-
Fibronectin splice isoforms in wound healing and vascular development
title Fibronectin splice isoforms in wound healing and vascular development
title_full Fibronectin splice isoforms in wound healing and vascular development
title_fullStr Fibronectin splice isoforms in wound healing and vascular development
title_full_unstemmed Fibronectin splice isoforms in wound healing and vascular development
title_short Fibronectin splice isoforms in wound healing and vascular development
title_sort fibronectin splice isoforms in wound healing and vascular development
topic Biology.
url http://hdl.handle.net/1721.1/29909
work_keys_str_mv AT burrowsstephanieyvonne1974 fibronectinspliceisoformsinwoundhealingandvasculardevelopment