Fibronectin splice isoforms in wound healing and vascular development

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.

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Biology.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2002

Author dc:creator

• Burrows, Stephanie Yvonne, 1974-

Advisor dc:contributor.advisor

• Richard O. Hynes.

• Biology.

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.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/29909

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/29909