The divergence-convergence model of acquired neuroprotection

被引:11
作者
Bas-Orth, Carlos [1 ]
Bading, Hilmar [1 ]
机构
[1] Heidelberg Univ, Interdisciplinary Ctr Neurosci, Dept Neurobiol, D-69120 Heidelberg, Germany
关键词
Calcium signaling; Gene transcription; Apoptosis; Programmed cell death; Synapse to nucleus communication; Gene network; MITOCHONDRIAL PERMEABILITY TRANSITION; ACTIVITY-DEPENDENT NEUROPROTECTION; STEM AUDITORY NUCLEI; SYNAPTIC ACTIVITY; CELL-DEATH; AFFERENT INFLUENCES; POSITIVE FEEDBACK; NEURONAL SURVIVAL; ACTION-POTENTIALS; NMDA RECEPTORS;
D O I
10.1016/j.mod.2012.09.008
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
It is commonly known that mental activity helps to maintain a healthy brain. Recent research has unraveled the underlying molecular mechanisms that explain why an active brain lives longer. These mechanisms involve the activation of a comprehensive transcriptional program that is triggered by enhanced synaptic activity and renders neurons resistant to harmful conditions. Functionally, this state of acquired neuroprotection may be achieved mainly via one mechanism, which is the stabilization of mitochondria. In this review we propose a model that describes the signaling network that links synaptic activity to neuroprotection. We suggest that the divergent-convergent architecture of this signaling network ensures both robust and reliable as well as persistent activation of the neuroprotective machinery. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:396 / 401
页数:6
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