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Bcl-XL mediates epidermal growth factor dependent cell survival in HC11 mammary epithelial cells
- Source :
- Biochim. Biophys. Acta Mol. Cell Res. 2009;1793(3):496-505, Biblioteca Digital (UBA-FCEN), Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales, instacron:UBA-FCEN
- Publisher :
- Elsevier B.V.
-
Abstract
- Apoptosis is the predominant process controlling cell deletion during post-lactational mammary gland remodeling. The members of the Bcl-2 protein family, whose expression levels are under the control of lactogenic hormones, internally control this mechanism. Epidermal growth factor (EGF) belongs to a family of proteins that act as survival factors for mammary epithelial cells upon binding to specific membrane tyrosine kinase receptors. Expression of EGF peaks during lactation and dramatically decreases in the involuting mammary gland. Though it was suggested that the protective effect of EGF is mediated through the phosphatidylinositol-3-kinase (PI3K) or MEK/ERK kinases activities, little is known about the downstream mechanisms involved on the anti-apoptotic effect of EGF on mammary epithelial cells; particularly the identity of target genes controlling apoptosis. Here, we focused on the effect of EGF on the survival of mammary epithelial cells. We particularly aimed at the characterization of the signaling pathways that were triggered by this growth factor, impinge upon expression of Bcl-2 family members and therefore have an impact on the regulation of cell survival. We demonstrate that EGF provokes the induction of the anti-apoptotic isoform Bcl-XL and the phosphorylation and down-regulation of the pro-apoptotic protein Bad. The activation of JNK and PI3K/AKT signaling pathways promotes the induction of Bcl-XL while AKT activation also leads to Bad phosphorylation and down-regulation. This protective effect of EGF correlates mainly with the up-regulation of Bcl-XL than with the down-regulation of Bad. In fact, HC11 cells unable to express bcl-X, die even in the presence of EGF. In this context, Bcl-XL emerges as a key anti-apoptotic molecule critical for mediating EGF cell survival. © 2008 Elsevier B.V. All rights reserved. Fil:Romorini, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Coso, O.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Pecci, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
- Subjects :
- MAPK/ERK pathway
protein bcl x
Apoptosis
animal cell
stress activated protein kinase
Receptor tyrosine kinase
protein induction
Mice
Phosphatidylinositol 3-Kinases
Epidermal growth factor
mitochondrion
1-Phosphatidylinositol 3-Kinase
animal
genetics
phosphatidylinositol 3 kinase
Phosphorylation
protein bcl xl
biology
Kinase
article
Cytochromes c
Cell biology
Mitochondria
cytochrome c
epidermal growth factor
female
priority journal
udder
recombinant epidermal growth factor
Female
bcl-Associated Death Protein
breast epithelium
Signal transduction
down regulation
signal transduction
protein bcl 2
Bcl-XL
Cell Survival
bcl-X Protein
Down-Regulation
Mammary epithelial cell
protein BAD
Mammary Glands, Animal
MAPKs
protein secretion
Animals
Humans
Bad
controlled study
human
protein expression
Protein kinase B
Molecular Biology
mouse
PI3K/AKT/mTOR pathway
EGF
nonhuman
Epidermal Growth Factor
JNK Mitogen-Activated Protein Kinases
Epithelial Cells
enzyme activation
Cell Biology
protein family
protein phosphorylation
mitogen activated protein kinase 3
mitogen activated protein kinase 1
biology.protein
protein kinase B
epithelium cell
metabolism
Proto-Oncogene Proteins c-akt
Subjects
Details
- Language :
- English
- ISSN :
- 01674889
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
- Accession number :
- edsair.doi.dedup.....c88636276b3c82de48f89aa62c6772f2
- Full Text :
- https://doi.org/10.1016/j.bbamcr.2008.12.002