Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/49593

TitleAP2γ controls adult hippocampal neurogenesis and modulates cognitive, but not anxiety or depressive-like behavior
Author(s)Pinheiro, António Maria Restolho Mateus
Alves, N. D.
Patrício, Patrícia Carvalho
Santos, Ana Rita Machado dos
Campos, E. Loureiro
Silva, Joana Margarida Gonçalves Mota
Sardinha, Vanessa Alexandra Morais
Reis, Joana Vanessa Santos
Schorle, H.
Oliveira, João Filipe Pedreira de
Ninkovic, J.
Sousa, Nuno Jorge Carvalho
Pinto, Luísa Alexandra Meireles
Issue date2017
PublisherNature Publishing Group
JournalMolecular Psychiatry
Abstract(s)Hippocampal neurogenesis has been proposed to participate in a myriad of behavioral responses, both in basal states and in the context of neuropsychiatric disorders. Here, we identify activating protein 2γ 3 (AP2γ 3, also known as Tcfap2c), originally described to regulate the generation of neurons in the developing cortex, as a modulator of adult hippocampal glutamatergic neurogenesis in mice. Specifically, AP2γ 3 is present in a sub-population of hippocampal transient amplifying progenitors. There, it is found to act as a positive regulator of the cell fate determinants Tbr2 and NeuroD, promoting proliferation and differentiation of new glutamatergic granular neurons. Conditional ablation of AP2γ 3 in the adult brain significantly reduced hippocampal neurogenesis and disrupted neural coherence between the ventral hippocampus and the medial prefrontal cortex. Furthermore, it resulted in the precipitation of multimodal cognitive deficits. This indicates that the sub-population of AP2γ 3-positive hippocampal progenitors may constitute an important cellular substrate for hippocampal-dependent cognitive functions. Concurrently, AP2γ 3 deletion produced significant impairments in contextual memory and reversal learning. More so, in a water maze reference memory task a delay in the transition to cognitive strategies relying on hippocampal function integrity was observed. Interestingly, anxiety- and d epressive-like behaviors were not significantly affected. Altogether, findings open new perspectives in understanding the role of specific sub-populations of newborn neurons in the (patho)physiology of neuropsychiatric disorders affecting hippocampal neuroplasticity and cognitive function in the adult brain.
TypeArticle
URIhttp://hdl.handle.net/1822/49593
DOI10.1038/mp.2016.169
ISSN1662-5153
Publisher versionhttps://www.nature.com
Peer-Reviewedyes
AccessOpen access
Appears in Collections:ICVS - Artigos em Revistas Internacionais com Referee

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