Gauducheau Manon, Lemaire-Mayo Valerie, D'Amato Francesca R, Oddi Diego, Crusio Wim E, Pietropaolo Susanna
Univ. Bordeaux, INCIA, Pessac cedex, France.
CNRS, INCIA, UMR 5287, Pessac cedex, France.
Autism Res. 2017 Jun;10(6):1067-1078. doi: 10.1002/aur.1743. Epub 2017 Mar 16.
Fragile X syndrome (FXS) is a major developmental disorder and the most frequent monogenic cause of autism. Surprisingly, most existing studies on the Fmr1-KO mouse model for FXS have focused on males, although FX women, who are mostly heterozygous for the Fmr1 mutation, are known to exhibit several behavioral deficits, including autistic-like features. Furthermore, most animal research has been carried out on adults only; so that little is known about the age progression of the behavioral phenotype of Fmr1 mutants, which is a crucial issue to optimize the impact of therapeutic interventions. Here, we performed an extensive analysis of autistic-like social behaviors in heterozygous (HET) Fmr1-KO females and their WT littermates at different ages. No behavioral difference between HET and WT mice was observed at infancy, but some abnormalities in social interaction and communication were first detected at juvenile age. At adulthood some of these alterations disappeared, but avoidance of social novelty appeared, together with other FXS-relevant behavioral deficits, such as hyperactivity and reduced contextual fear response. Our data provide for the first time evidence for the presence of autistic-relevant behavioral abnormalities in Fmr1-HET female mice, demonstrating the utility of this mouse line to model autistic-like behaviors in both sexes. These results also highlight the importance of taking into account age differences when using the Fmr1-KO mouse model, suggesting that the early post-natal phases are the most promising target for preventive interventions and the adult age is the most appropriate to investigate the behavioral impact of potential therapies. Autism Res 2017. © 2017 International Society for Autism Research, Wiley Periodicals, Inc. Autism Res 2017, 10: 1067-1078. © 2017 International Society for Autism Research, Wiley Periodicals, Inc.
脆性X综合征(FXS)是一种主要的发育障碍,也是自闭症最常见的单基因病因。令人惊讶的是,尽管已知Fmr1突变大多为杂合子的FX女性表现出包括自闭症样特征在内的多种行为缺陷,但现有的大多数关于FXS的Fmr1基因敲除(KO)小鼠模型的研究都集中在雄性小鼠上。此外,大多数动物研究仅在成年动物中进行;因此,对于Fmr1突变体行为表型的年龄进展知之甚少,而这是优化治疗干预效果的关键问题。在这里,我们对不同年龄的杂合(HET)Fmr1-KO雌性小鼠及其野生型同窝小鼠的自闭症样社交行为进行了广泛分析。在婴儿期,未观察到HET小鼠和野生型小鼠之间的行为差异,但在幼年时首次检测到社交互动和交流方面的一些异常。在成年期,其中一些改变消失了,但出现了对社交新奇性的回避,以及其他与FXS相关的行为缺陷,如多动和情境恐惧反应降低。我们的数据首次为Fmr1-HET雌性小鼠中存在与自闭症相关的行为异常提供了证据,证明了该小鼠品系在模拟两性自闭症样行为方面的实用性。这些结果还强调了在使用Fmr1-KO小鼠模型时考虑年龄差异的重要性,表明出生后早期阶段是预防性干预最有希望的目标,而成年期是研究潜在疗法行为影响的最合适阶段。《自闭症研究》2017年。©2017国际自闭症研究协会,威利期刊公司。《自闭症研究》2017年,10: 1067 - 1078。©2017国际自闭症研究协会,威利期刊公司。