Generating new neurons to circumvent your fears: the role of IGF signaling

被引:35
作者
Agis-Balboa, R. C. [1 ]
Fischer, A. [1 ,2 ]
机构
[1] Univ Med Ctr Gottingen, Dept Psychiat & Psychotherapy, D-37077 Gottingen, Germany
[2] German Ctr Neurodegenerat Dis DZNE Gottingen, D-37077 Gottingen, Germany
关键词
IGF2; IGFBP7; Neurogenesis; Fear extinction; Learning and memory; Epigenetics; GROWTH-FACTOR-I; ADULT HIPPOCAMPAL NEUROGENESIS; NEURAL STEM-CELLS; MEDIAL PREFRONTAL CORTEX; LONG-TERM-MEMORY; POSTTRAUMATIC-STRESS-DISORDER; ENHANCED SYNAPTIC PLASTICITY; ACTIVATED PROTEIN-KINASE; CENTRAL-NERVOUS-SYSTEM; DENTATE GRANULE CELLS;
D O I
10.1007/s00018-013-1316-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Extinction of fear memory is a particular form of cognitive function that is of special interest because of its involvement in the treatment of anxiety and mood disorders. Based on recent literature and our previous findings (EMBO J 30(19):4071-4083, 2011), we propose a new hypothesis that implies a tight relationship among IGF signaling, adult hippocampal neurogenesis and fear extinction. Our proposed model suggests that fear extinction-induced IGF2/IGFBP7 signaling promotes the survival of neurons at 2-4 weeks old that would participate in the discrimination between the original fear memory trace and the new safety memory generated during fear extinction. This is also called "pattern separation", or the ability to distinguish similar but different cues (e.g., context). To understand the molecular mechanisms underlying fear extinction is therefore of great clinical importance.
引用
收藏
页码:21 / 42
页数:22
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