The Alpha7beta1 Integrin in Skeletal Muscle and Muscular Dystrophy
Liu, Jianming
This item is only available for download by members of the University of Illinois community. Students, faculty, and staff at the U of I may log in with your NetID and password to view the item. If you are trying to access an Illinois-restricted dissertation or thesis, you can request a copy through your library's Inter-Library Loan office or purchase a copy directly from ProQuest.
Permalink
https://hdl.handle.net/2142/86698
Description
Title
The Alpha7beta1 Integrin in Skeletal Muscle and Muscular Dystrophy
Author(s)
Liu, Jianming
Issue Date
2007
Doctoral Committee Chair(s)
Kaufman, Stephen J.
Department of Study
Microbiology
Discipline
Microbiology
Degree Granting Institution
University of Illinois at Urbana-Champaign
Degree Name
Ph.D.
Degree Level
Dissertation
Keyword(s)
Biology, Molecular
Language
eng
Abstract
This thesis examines the effects of enhancing alpha7 integrin on cellular functions and global gene expression in myoblasts and skeletal muscle. I found that 3-fold more alpha7 integrin promotes myoblast adhesion, proliferation and resistance to apoptosis without affecting differentiation. In addition, 8-fold more alpha7 integrin in skeletal muscle is not toxic and has no adverse effects in alpha7 integrin transgenic mice. Moreover, enhancing alpha7 integrin only minimally affects global gene expression in myoblasts and skeletal muscle. Thus, increasing alpha7 integrin is a promising therapeutic approach for treating Duchenne muscular dystrophy as it can reinforce the association between the extracellular matrix and actin cytoskeleton without interfering with normal cell functions or gene expression. In this dissertation I also demonstrate that beta1 integrin is a limiting factor for the compensatory effects of enhanced alpha7 integrin in skeletal muscle and my results suggest that increasing both alpha7 and beta1 integrin chains may be a more effective strategy for treating muscular dystrophy. In addition, I report the discovery of a species-specific proteolytic cleavage of the alpha7 integrin chain and demonstrate this cleavage regulates integrin mediated cellular functions. The potential involvement of this proteolytic cleavage in muscular dystrophy is also discussed. Together, this dissertation explores the functions of the alpha7beta1 integrin in skeletal muscle and its potential use as a treatment for muscular dystrophy.
Use this login method if you
don't
have an
@illinois.edu
email address.
(Oops, I do have one)
IDEALS migrated to a new platform on June 23, 2022. If you created
your account prior to this date, you will have to reset your password
using the forgot-password link below.