We initially identified a nuclear protein, prothymosin-α1 (ProTα), as a key protein inhibiting necrosis by subjecting conditioned media from serum-free cultures of cortical neurons to a few chromatography steps. ProTα inhibited necrosis of cultured neurons by preventing rapid loss of cellular adenosine triphosphate levels by reversing the decreased membrane localization of glucose transporters but caused apoptosis through up-regulation of proapoptotic Bcl2-family proteins. The apoptosis caused by ProTα was further inhibited by growth factors, including brain-derived neurotrophic factor. The ProTα-induced cell death mode switch from necrosis to apoptosis was also reproduced in experimental ischemia-reperfusion culture experiments, although the apoptosis level was markedly reduced, possibly because of the presence of growth factors in the reperfused serum. Knock down of PKCβII expression prevented this cell death mode switch. Collectively, these results suggest that ProTα is an extracellular signal protein that acts as a cell death mode switch and could be a promising candidate for preventing brain strokes with the help of known apoptosis inhibitors.
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12 March 2007
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March 12 2007
Identification of prothymosin-α1, the necrosis–apoptosis switch molecule in cortical neuronal cultures
Hiroshi Ueda,
Hiroshi Ueda
Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan
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Ryousuke Fujita,
Ryousuke Fujita
Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan
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Akira Yoshida,
Akira Yoshida
Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan
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Hayato Matsunaga,
Hayato Matsunaga
Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan
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Mutsumi Ueda
Mutsumi Ueda
Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan
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Hiroshi Ueda
Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan
Ryousuke Fujita
Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan
Akira Yoshida
Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan
Hayato Matsunaga
Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan
Mutsumi Ueda
Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan
Correspondence to Hiroshi Ueda: [email protected]
Abbreviations used in this paper: AS-ODN, antisense ODN; BDNF, brain-derived neurotrophic factor; CM, conditioned medium; HD, high-density; LD, low-density; LOG, low-oxygen and low-glucose; MALDI-TOF, matrix-assisted laser desorption/ionization–time of flight; MS, mass spectrometry; ODN, oligodeoxynucleotide; PI, propidium iodide; ProTα, prothymosin-α1.
Received:
August 04 2006
Accepted:
February 06 2007
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2007
J Cell Biol (2007) 176 (6): 853–862.
Article history
Received:
August 04 2006
Accepted:
February 06 2007
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Hiroshi Ueda, Ryousuke Fujita, Akira Yoshida, Hayato Matsunaga, Mutsumi Ueda; Identification of prothymosin-α1, the necrosis–apoptosis switch molecule in cortical neuronal cultures . J Cell Biol 12 March 2007; 176 (6): 853–862. doi: https://doi.org/10.1083/jcb.200608022
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