DESCRIPTION:

Genes that were differentially expressed during fear extinction FDR < 5%; fold change log2 ≥1) after 1 extinction trial(high freezing with C57BL/6. Statistics reported as fold change.

LABEL:

Dif Exp - Fear - High freezing

SCORE TYPE:

Correlation

THRESHOLD:

0 <=> 1

GENES IN THRESHOLD:

6

DATE ADDED:

None

DATE UPDATED:

2024-10-22

SPECIES:

AUTHORS:

Agis-Balboa RC, Arcos-Diaz D, Wittnam J, Govindarajan N, Blom K, Burkhardt S, Haladyniak U, Agbemenyah HY, Zovoilis A, Salinas-Riester G, Opitz L, Sananbenesi F, Fischer A

TITLE:

A hippocampal insulin-growth factor 2 pathway regulates the extinction of fear memories.

JOURNAL:

The EMBO journal Aug 2011, Vol 30, pp. 4071-83

ABSTRACT:

Extinction learning refers to the phenomenon that a previously learned response to an environmental stimulus, for example, the expression of an aversive behaviour upon exposure to a specific context, is reduced when the stimulus is repeatedly presented in the absence of a previously paired aversive event. Extinction of fear memories has been implicated with the treatment of anxiety disease but the molecular processes that underlie fear extinction are only beginning to emerge. Here, we show that fear extinction initiates upregulation of hippocampal insulin-growth factor 2 (Igf2) and downregulation of insulin-growth factor binding protein 7 (Igfbp7). In line with this observation, we demonstrate that IGF2 facilitates fear extinction, while IGFBP7 impairs fear extinction in an IGF2-dependent manner. Furthermore, we identify one cellular substrate of altered IGF2 signalling during fear extinction. To this end, we show that fear extinction-induced IGF2/IGFBP7 signalling promotes the survival of 17-19-day-old newborn hippocampal neurons. In conclusion, our data suggest that therapeutic strategies that enhance IGF2 signalling and adult neurogenesis might be suitable to treat disease linked to excessive fear memory. PUBMED: 21873981
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