scholarly journals Enlarged Brain Ventricles and Impaired Neurogenesis in the Ts1Cje and Ts2Cje Mouse Models of Down Syndrome

2009 ◽  
Vol 20 (5) ◽  
pp. 1131-1143 ◽  
Author(s):  
Keiichi Ishihara ◽  
Kenji Amano ◽  
Eiichi Takaki ◽  
Atsushi Shimohata ◽  
Haruhiko Sago ◽  
...  
Genes ◽  
2021 ◽  
Vol 12 (10) ◽  
pp. 1598
Author(s):  
Keiichi Ishihara

Down syndrome (DS), also known as trisomy 21, is the most frequent genetic cause of intellectual disability. Although the mechanism remains unknown, delayed brain development is assumed to be involved in DS intellectual disability. Analyses with human with DS and mouse models have shown that defects in embryonic cortical neurogenesis may lead to delayed brain development. Cre-loxP-mediated chromosomal engineering has allowed the generation of a variety of mouse models carrying various partial Mmu16 segments. These mouse models are useful for determining genotype–phenotype correlations and identifying dosage-sensitive genes involved in the impaired neurogenesis. In this review, we summarize several candidate genes and pathways that have been linked to defective cortical neurogenesis in DS.


2021 ◽  
Vol 535 ◽  
pp. 87-92
Author(s):  
Ryohei Shimizu ◽  
Keiichi Ishihara ◽  
Eri Kawashita ◽  
Haruhiko Sago ◽  
Kazuhiro Yamakawa ◽  
...  

2021 ◽  
Vol 15 ◽  
Author(s):  
Cesar Sierra ◽  
Ilario De Toma ◽  
Lorenzo Lo Cascio ◽  
Esteban Vegas ◽  
Mara Dierssen

The use of mouse models has revolutionized the field of Down syndrome (DS), increasing our knowledge about neuropathology and helping to propose new therapies for cognitive impairment. However, concerns about the reproducibility of results in mice and their translatability to humans have become a major issue, and controlling for moderators of behavior is essential. Social and environmental factors, the experience of the researcher, and the sex and strain of the animals can all have effects on behavior, and their impact on DS mouse models has not been explored. Here we analyzed the influence of a number of social and environmental factors, usually not taken into consideration, on the behavior of male and female wild-type and trisomic mice (the Ts65Dn model) in one of the most used tests for proving drug effects on memory, the novel object recognition (NOR) test. Using principal component analysis and correlation matrices, we show that the ratio of trisomic mice in the cage, the experience of the experimenter, and the timing of the test have a differential impact on male and female and on wild-type and trisomic behavior. We conclude that although the NOR test is quite robust and less susceptible to environmental influences than expected, to obtain useful results, the phenotype expression must be contrasted against the influences of social and environmental factors.


2018 ◽  
Vol 11 (6) ◽  
pp. dmm031013 ◽  
Author(s):  
Nadine M. Aziz ◽  
Faycal Guedj ◽  
Jeroen L. A. Pennings ◽  
Jose Luis Olmos-Serrano ◽  
Ashley Siegel ◽  
...  

2019 ◽  
Vol 30 (1) ◽  
pp. 75-91 ◽  
Author(s):  
Keiichi Ishihara ◽  
Ryohei Shimizu ◽  
Kazuyuki Takata ◽  
Eri Kawashita ◽  
Kenji Amano ◽  
...  

2020 ◽  
Vol 61 (5) ◽  
pp. 25
Author(s):  
Daniella B. Victorino ◽  
Jonah J. Scott-McKean ◽  
Mark W. Johnson ◽  
Alberto C. S. Costa

2017 ◽  
Vol 105 ◽  
pp. 235-244 ◽  
Author(s):  
Alain D. Dekker ◽  
Yannick Vermeiren ◽  
Christelle Albac ◽  
Eva Lana-Elola ◽  
Sheona Watson-Scales ◽  
...  

2001 ◽  
Vol 35 (2) ◽  
pp. 115-145 ◽  
Author(s):  
Zygmunt Galdzicki ◽  
Richard Siarey ◽  
Rosalyn Pearce ◽  
James Stoll ◽  
Stanley I. Rapoport

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