期刊
BMC RESEARCH NOTES
卷 14, 期 1, 页码 -出版社
SPRINGERNATURE
DOI: 10.1186/s13104-020-05436-0
关键词
Light-sheet microscopy; Chd8; Mouse brains; Autism; Tissue clearing; Morphometry; Lewis' law; Aboavweaire's law
资金
- SNF Sinergia grant
This study utilized light-sheet fluorescence microscopy to examine measurable brain alterations in Chd8(+/-) mice at early embryonic stages, revealing differences in brain morphology compared to wild-type mice. The findings suggest the potential for exploring the etiology and cellular basis of Chd8 haploinsufficiency through high-resolution microscopy technologies and multi-scale morphometric analyses.
Objective: Autism spectrum disorder (ASD) encompasses a group of neurodevelopmental conditions that remain poorly understood due to their genetic complexity. CHD8 is a risk allele strongly associated with ASD, and heterozygous Chd8 loss-of-function mice have been reported to exhibit macrocephaly in early postnatal stages. In this work, we sought to identify measurable brain alterations in early embryonic development. Results: We performed light-sheet fluorescence microscopy imaging of N-cadherin stained and optically cleared Chd8(+/-) and wild-type mouse brains at embryonic day 12.5 (E12.5). We report a detailed morphometric characterization of embryonic brain shapes and cortical neuroepithelial apical architecture. While Chd8(+/-) characteristic expansion of the forebrain and midbrain was not observed this early in embryogenesis, a tendency for a decreased lateral ventricular sphericity and an increased intraocular distance in Chd8(+/-) brains was found compared to controls. This study advocates the use of high-resolution microscopy technologies and multi-scale morphometric analyses of target brain regions to explore the etiology and cellular basis of Chd8 haploinsufficiency.
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