Schmalzigaug Robert, Rodriguiz Ramona M, Bonner Pamela E, Davidson Collin E, Wetsel William C, Premont Richard T
Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.
Neurosci Lett. 2009 Jul 17;458(2):79-83. doi: 10.1016/j.neulet.2009.04.037. Epub 2009 Apr 19.
G protein-coupled receptor kinase interacting protein 1 (GIT1) belongs to the family of Arf GAP proteins and has been implicated in the regulation of G protein-coupled receptor (GPCR) sequestration, cell migration, synapse formation and dendritic spine morphogenesis in neurons. To extend these cellular studies on GIT1 to an in vivo system, we generated mice with globally inactivated Git1 gene by breeding mice carrying a conditional Git1(flox) allele with mice expressing the CMV-Cre transgene. Although many GIT1 knockout (GIT1-KO) animals died shortly after birth, homozygous mutants that survived the early post-partum period developed normally into adulthood and were fertile. Behavioral analyses of adult GIT1-KO mice revealed normal exploratory, anxiety- and depressive-like behaviors. However, GIT1-KO mice show impaired responses to fear conditioning and fear-potentiated startle. Overall, these findings suggest that GIT1 is involved in the regulation of amygdala-mediated experience-based emotional behaviors.
G蛋白偶联受体激酶相互作用蛋白1(GIT1)属于Arf GAP蛋白家族,与G蛋白偶联受体(GPCR)的隔离、细胞迁移、突触形成以及神经元树突棘形态发生的调节有关。为了将这些关于GIT1的细胞研究扩展到体内系统,我们通过将携带条件性Git1(flox)等位基因的小鼠与表达CMV-Cre转基因的小鼠杂交,培育出了全局Git1基因失活的小鼠。尽管许多GIT1基因敲除(GIT1-KO)动物在出生后不久死亡,但在产后早期存活下来的纯合突变体正常发育至成年且具有生育能力。对成年GIT1-KO小鼠的行为分析显示其探索、焦虑和抑郁样行为正常。然而,GIT1-KO小鼠对恐惧条件反射和恐惧增强惊吓的反应受损。总体而言,这些发现表明GIT1参与杏仁核介导的基于经验的情绪行为的调节。