Schizophrenia: What's Arc Got to Do with It?

被引:12
作者
Manago, Francesca [1 ]
Papaleo, Francesco [1 ]
机构
[1] Ist Italiano Tecnol, Dept Neurosci & Brain Technol, Genoa, Italy
关键词
behavior; RDoC; dopamine; glutamate; immediate early gene; Arg3.1; mice; IMMEDIATE-EARLY GENE; VENTRAL TEGMENTAL AREA; LONG-TERM POTENTIATION; METHYL-D-ASPARTATE; DE-NOVO MUTATIONS; SYNAPTIC PLASTICITY; PREFRONTAL CORTEX; TEMPORAL-ORDER; PREPULSE INHIBITION; COGNITIVE DEFICITS;
D O I
10.3389/fnbeh.2017.00181
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Human studies of schizophrenia are now reporting a previously unidentified genetic convergence on postsynaptic signaling complexes such as the activity-regulated cytoskeletal-associated (Arc) gene. However, because this evidence is still very recent, the neurobiological implication of Arc in schizophrenia is still scattered and unrecognized. Here, we first review current and developing findings connecting Arc in schizophrenia. We then highlight recent and previous findings from preclinical mouse models that elucidate how Arc genetic modifications might recapitulate schizophrenia-relevant behavioral phenotypes following the novel Research Domain Criteria (RDoC) framework. Building on this, we finally compare and evaluate several lines of evidence demonstrating that Arc genetics can alter both glutamatergic and dopaminergic systems in a very selective way, again consistent with molecular alterations characteristic of schizophrenia. Despite being only initial, accumulating and compelling data are showing that Arc might be one of the primary biological players in schizophrenia. Synaptic plasticity alterations in the genetic architecture of psychiatric disorders might be a rule, not an exception. Thus, we anticipate that additional evidence will soon emerge to clarify the Arc-dependent mechanisms involved in the psychiatric-related dysfunctional behavior.
引用
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页数:11
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