Autoantibodies to p75/LEDGF, a cell survival factor, found in patients with atypical retinal degeneration

2006 ◽  
Vol 27 (1) ◽  
pp. 17-27 ◽  
Author(s):  
Marian S. Chin ◽  
Rafael C. Caruso ◽  
Barbara Detrick ◽  
John J. Hooks
2010 ◽  
Vol 21 (4) ◽  
pp. 499-500 ◽  
Author(s):  
Martin A. Schwartz

In 1992, Jere Meredith and I followed up on a serendipitous observation and showed that matrix deprivation can lead to apoptosis. Our article in Molecular Biology of the Cell, together with work form Steve Frisch's lab, helped establish the paradigm that integrin signals control cell survival in a variety of systems. It has been a pleasure to watch that work take on a life of its own as other investigators have explored its role in processes such as cavitation, regression of the mammary gland at the end of pregnancy, cancer metastasis, and tumor resistance to chemotherapy. Recently, we described an exception to the paradigm: In some tumors, reagents that activate integrin signaling enhance apoptosis in response to chemotherapy.


1993 ◽  
Vol 4 (9) ◽  
pp. 953-961 ◽  
Author(s):  
J E Meredith ◽  
B Fazeli ◽  
M A Schwartz

Programmed cell death (PCD) or apoptosis is a naturally occurring cell suicide pathway induced in a variety of cell types. In many cases, PCD is induced by the withdrawal of specific hormones or growth factors that function as survival factors. In this study, we have investigated the potential role of the extracellular matrix (ECM) as a cell survival factor. Our results indicate that in the absence of any ECM interactions, human endothelial cells rapidly undergo PCD, as determined by cell morphology, nuclei fragmentation, DNA degradation, protein cross-linking, and the expression of the PCD-specific gene TRPM-2. PCD was blocked by plating cells on an immobilized integrin beta 1 antibody but not by antibodies to either the class I histocompatibility antigen (HLA) or vascular cell adhesion molecule-1 (VCAM-1), suggesting that integrin-mediated signals were required for maintaining cell viability. Treatment of the cells in suspension with the tyrosine phosphatase inhibitor sodium orthovanadate also blocked PCD. When other cell types were examined, some, but not all, underwent rapid cell death when deprived of adhesion to the ECM. These results suggest that in addition to regulating cell growth and differentiation, the ECM also functions as a survival factor for many cell types.


PLoS ONE ◽  
2016 ◽  
Vol 11 (8) ◽  
pp. e0160970 ◽  
Author(s):  
Iana H. Haralambieva ◽  
Michael T. Zimmermann ◽  
Inna G. Ovsyannikova ◽  
Diane E. Grill ◽  
Ann L. Oberg ◽  
...  

Apmis ◽  
2008 ◽  
Vol 116 (5) ◽  
pp. 413-413
Author(s):  
Lou Klitgaard Povlsen ◽  
Mads Daugaard ◽  
Mikkel Rohde ◽  
Jakob E. Larsen ◽  
Marja Jäättelä

2004 ◽  
Vol 77 (1) ◽  
pp. 9-14 ◽  
Author(s):  
A. Dahl ◽  
P.S. Eriksson ◽  
P. Davidsson ◽  
A.I. Persson ◽  
R. Ekman ◽  
...  

2013 ◽  
Vol 131 (2) ◽  
pp. AB192
Author(s):  
Kanami Orihara ◽  
Sonia S. Charran ◽  
Kent T. HayGlass ◽  
Redwan Moqbel

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