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Akt plays a central role in the anti-apoptotic effect of estrogen in endothelial cells
- Source :
- Biochemical and biophysical research communications. 324(1)
- Publication Year :
- 2004
-
Abstract
- Estrogen has been reported to inhibit apoptosis in vascular endothelial cells. However, its precise mechanism still remains to be elucidated. Here we determined the role of Akt in the anti-apoptotic effect of estrogen. 17β-Estradiol prevented the apoptosis induced by TNF-α in bovine aortic endothelial cells, as evaluated by double staining with fluorescein isothiocyanate-conjugated annexin V and propidium iodide. Introducing a dominant negative mutant of Akt by using a cell-penetrating peptide of Tat protein inhibited the anti-apoptotic effect of estrogen in a concentration-dependent manner, and resulted in the complete inhibition of the anti-apoptotic effect of 17β-estradiol at 1 nM and higher concentrations. The dominant negative mutant without the cell-penetrating peptide and Tat peptide-conjugated protein A had no effect. The intracellular protein transduction was confirmed by immunoblot analysis. Our observations thus provide first direct evidence that Akt plays a central role in the anti-apoptotic effect of estrogen in vascular endothelial cells.
- Subjects :
- medicine.drug_class
Recombinant Fusion Proteins
Biophysics
Peptide
Apoptosis
Biology
Protein Serine-Threonine Kinases
Biochemistry
chemistry.chemical_compound
Annexin
Proto-Oncogene Proteins
medicine
Animals
Humans
Propidium iodide
Molecular Biology
Protein kinase B
Cells, Cultured
chemistry.chemical_classification
Tumor Necrosis Factor-alpha
Endothelial Cells
Estrogens
Cell Biology
Molecular biology
Cell biology
Endothelial stem cell
chemistry
Estrogen
Gene Products, tat
Mutation
biology.protein
Cattle
Endothelium, Vascular
Protein A
Peptides
Proto-Oncogene Proteins c-akt
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 324
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Biochemical and biophysical research communications
- Accession number :
- edsair.doi.dedup.....7eb256b4d8e2183e28fc82a1740bbd97