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Science 22 October 1999: Vol. 286. no. 5440, pp. 785 - 790 DOI: 10.1126/science.286.5440.785
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Reports
Neuronal Activity-Dependent Cell Survival Mediated by Transcription Factor MEF2
Zixu Mao,
1*
Azad Bonni,
1
Fen Xia,
2
Mireya Nadal-Vicens,
1
Michael E. Greenberg
1
During mammalian development, electrical activity promotes
the calcium-dependent survival of neurons that have made appropriate synaptic connections. However, the mechanisms by which calcium mediates
neuronal survival during development are not well characterized. A
transcription-dependent mechanism was identified by which calcium influx into neurons promoted cell survival. The transcription factor
MEF2 was selectively expressed in newly generated postmitotic neurons
and was required for the survival of these neurons. Calcium influx into
cerebellar granule neurons led to activation of p38 mitogen-activated
protein kinase-dependent phosphorylation and activation of
MEF2. Once activated, MEF2 regulated neuronal survival by stimulating
MEF2-dependent gene transcription. These findings demonstrate that MEF2
is a calcium-regulated transcription factor and define a function for
MEF2 during nervous system development that is distinct from previously
well-characterized functions of MEF2 during muscle differentiation.
1 Division of Neuroscience, Department of
Neurology, Children's Hospital and Department of Neurobiology, Harvard
Medical School, Boston, MA 02115, USA.
2 Department
of Radiation Oncology, Massachusetts General Hospital, Charlestown, MA
02129, USA.
*
Current address: The Liver Research Center, Rhode Island
Hospital and Department of Medicine, Brown University Medical School, Providence, RI 02903, USA.
To whom correspondence should be addressed. E-mail:
greenberg{at}a1.tch.harvard.edu
Read the Full Text
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- The nuclear localization domain of the MEF2 family of transcription factors shows member-specific features and mediates the nuclear import of histone deacetylase 4.
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- Silencing Mediator of Retinoid and Thyroid Hormone Receptors and Activating Signal Cointegrator-2 as Transcriptional Coregulators of the Orphan Nuclear Receptor Nur77.
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276, 43734-43739
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- Trafficking-Dependent and -Independent Pathways of Neurotransmitter Transporter Regulation Differentially Involving p38 Mitogen-Activated Protein Kinase Revealed in Studies of Insulin Modulation of Norepinephrine Transport in SK-N-SH Cells.
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J. Pharmacol. Exp. Ther.
299, 666-677
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- Signaling to the Nucleus by an L-type Calcium Channel-Calmodulin Complex Through the MAP Kinase Pathway.
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Science
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- An Essential Role for Rac/Cdc42 GTPases in Cerebellar Granule Neuron Survival.
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276, 39123-39131
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- Calcium regulation of neuronal gene expression.
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PNAS
98, 11024-11031
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- Identification of a Signal-Responsive Nuclear Export Sequence in Class II Histone Deacetylases.
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Mol. Cell. Biol.
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- Myocyte Enhancer Factor 2A and 2D Undergo Phosphorylation and Caspase-Mediated Degradation during Apoptosis of Rat Cerebellar Granule Neurons.
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- Neuronal CaV1.3{alpha}1 L-Type Channels Activate at Relatively Hyperpolarized Membrane Potentials and Are Incompletely Inhibited by Dihydropyridines.
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- 14-3-3{{tau}} associates with and activates the MEF2D transcription factor during muscle cell differentiation.
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- p38 Mitogen-Activated Protein Kinase Mediates Tumor Necrosis Factor-{{alpha}}-Induced Apoptosis in Rat Fetal Brown Adipocytes.
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Endocrinology
141, 4383-4395
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- Arsenite-Induced Apoptosis in Cortical Neurons Is Mediated by c-Jun N-Terminal Protein Kinase 3 and p38 Mitogen-Activated Protein Kinase.
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PNAS
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- A Protein Encoded within the Down Syndrome Critical Region Is Enriched in Striated Muscles and Inhibits Calcineurin Signaling.
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- Antiapoptotic role of the p38 mitogen-activated protein kinase-myocyte enhancer factor 2 transcription factor pathway during neuronal differentiation.
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PNAS
97, 7561-7566
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- Regulation of GLUT4 biogenesis in muscle: evidence for involvement of AMPK and Ca2+.
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Am J Physiol Endocrinol Metab
282, E1008-E1013
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