Zhao, Jianping
(2009)
Role of Focal Adhesion Protein Migfilin in the Regulation of Cell Survival and Cell Cycle.
Doctoral Dissertation, University of Pittsburgh.
(Unpublished)
Abstract
Integrin-mediated cell-extracellular matrix (ECM) adhesion is essential for the survival of normal epithelial cells, and loss of this cell-ECM adhesion leads to anoikis. In this dissertation study, we first identify migfilin, a novel focal adhesion protein, as a key sensor of cell-ECM adhesion in epithelial cells. Loss of cell-ECM adhesion significantly reduces migfilin protein levels in untransformed epithelial cells and concomitantly induces anoikis. Migfilin RNAi is sufficient to induce apoptosis in MCF-10A cells while overexpression of FLAG-migfilin partially protects these cells from anoikis, strongly suggesting that migfilin plays a critical role in cell adhesion-mediated cell survival signaling. Cell detachment-induced migfilin reduction is, at least partially, responsible for the induction of anoikis. Further signaling studies reveal that migfilin regulates cell survival and anoikis by influencing Src activation. Immunoflorescence staining shows that migfilin co-localizes with active Src in focal adhesions, and immunoprecipitation and GST pull-down assays demonstrate that migfilin directly interacts with Src. Moreover, the detailed structural studies show that migfilin strongly binds to the Src SH3 domain via the second PXXP cluster (140-173aa) in its proline-rich region, and weakly binds to the Src SH2 domain via an atypical binding sequence (E6KRVASS12) in its N-terminal. A working model is proposed in which migfilin promotes Src activation via direct interaction, and loss of cell-ECM adhesion triggers the degradation of migfilin protein, thereby causing Src inactivation which contributes to the initiation of anoikis. Interestingly, this migfilin-Src signaling pathway is dysfunctional in some anoikis-resistant cancer cells. During cell detachment, migfilin proteins are stabilized in these cancer cells, and phosph-Y419 Src levels are not reduced concomitantly, representing a novel mechanism for anoikis resistance during tumorigenesis. In addition, migfilin is found to negatively regulate p27 protein level. Depletion of migfilin significantly increases p27 protein levels in different cell lines. In HCT116 cells, migfilin RNAi increases both cytoplasmic and nuclear p27, and inhibits cell cycle progression. These findings indicate that migfilin provides a linkage between p27 and integrin-mediated cell-ECM adhesion.
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Details
| Item Type: |
University of Pittsburgh ETD
|
| Status: |
Unpublished |
| Creators/Authors: |
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| ETD Committee: |
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| Date: |
18 December 2009 |
| Date Type: |
Completion |
| Defense Date: |
23 November 2009 |
| Approval Date: |
18 December 2009 |
| Submission Date: |
16 December 2009 |
| Access Restriction: |
5 year -- Restrict access to University of Pittsburgh for a period of 5 years. |
| Institution: |
University of Pittsburgh |
| Schools and Programs: |
School of Medicine > Cellular and Molecular Pathology |
| Degree: |
PhD - Doctor of Philosophy |
| Thesis Type: |
Doctoral Dissertation |
| Refereed: |
Yes |
| Uncontrolled Keywords: |
apoptosis; cell adhesion; integrin; Src |
| Other ID: |
http://etd.library.pitt.edu/ETD/available/etd-12162009-145545/, etd-12162009-145545 |
| Date Deposited: |
10 Nov 2011 20:11 |
| Last Modified: |
19 Dec 2016 14:38 |
| URI: |
http://d-scholarship.pitt.edu/id/eprint/10397 |
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