Faculty Opinions recommendation of A role for intermediate radial glia in the tangential expansion of the mammalian cerebral cortex.

Author(s):  
Magdalena Goetz
Keyword(s):  
2001 ◽  
Vol 41 (1) ◽  
pp. 51-60 ◽  
Author(s):  
Nobuaki Tamamaki ◽  
Kouichi Nakamura ◽  
Keiko Okamoto ◽  
Takeshi Kaneko

2003 ◽  
Vol 100 (7) ◽  
pp. 4251-4256 ◽  
Author(s):  
R. S. Schmid ◽  
B. McGrath ◽  
B. E. Berechid ◽  
B. Boyles ◽  
M. Marchionni ◽  
...  

Nature ◽  
1974 ◽  
Vol 252 (5478) ◽  
pp. 55-56 ◽  
Author(s):  
A. BIGNAMI ◽  
D. DAHL

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Congyun Jin ◽  
Atsushi Yonezawa ◽  
Hiroki Yoshimatsu ◽  
Satoshi Imai ◽  
Madoka Koyanagi ◽  
...  

Abstract Riboflavin transporter 3 (RFVT3), encoded by the SLC52A3 gene, is important for riboflavin homeostasis in the small intestine, kidney, and placenta. Our previous study demonstrated that Slc52a3 knockout (Slc52a3−/−) mice exhibited neonatal lethality and metabolic disorder due to riboflavin deficiency. Here, we investigated the influence of Slc52a3 gene disruption on brain development using Slc52a3−/− embryos. Slc52a3−/− mice at postnatal day 0 showed hypoplasia of the brain and reduced thickness of cortical layers. At embryonic day 13.5, the formation of Tuj1+ neurons and Tbr2+ intermediate neural progenitors was significantly decreased; no significant difference was observed in the total number and proliferative rate of Pax6+ radial glia. Importantly, the hypoplastic phenotype was rescued upon riboflavin supplementation. Thus, it can be concluded that RFVT3 contributes to riboflavin homeostasis in embryos and that riboflavin itself is required during embryonic development of the cerebral cortex in mice.


2011 ◽  
Vol 136 (5) ◽  
pp. 515-526 ◽  
Author(s):  
Haoming Li ◽  
Guohua Jin ◽  
Jianbing Qin ◽  
Meiling Tian ◽  
Jinhong Shi ◽  
...  

Development ◽  
2012 ◽  
Vol 139 (3) ◽  
pp. 475-487 ◽  
Author(s):  
G. Mairet-Coello ◽  
A. Tury ◽  
E. Van Buskirk ◽  
K. Robinson ◽  
M. Genestine ◽  
...  

Cells ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 3
Author(s):  
Brandon L. Meyerink ◽  
Neeraj K. Tiwari ◽  
Louis-Jan Pilaz

Radial neuron migration in the developing cerebral cortex is a complex journey, starting in the germinal zones and ending in the cortical plate. In mice, migratory distances can reach several hundreds of microns, or millimeters in humans. Along the migratory path, radially migrating neurons slither through cellularly dense and complex territories before they reach their final destination in the cortical plate. This task is facilitated by radial glia, the neural stem cells of the developing cortex. Indeed, radial glia have a unique bipolar morphology, enabling them to serve as guides for neuronal migration. The key guiding structure of radial glia is the basal process, which traverses the entire thickness of the developing cortex. Neurons recognize the basal process as their guide and maintain physical interactions with this structure until the end of migration. Thus, the radial glia basal process plays a key role during radial migration. In this review, we highlight the pathways enabling neuron-basal process interactions during migration, as well as the known mechanisms regulating the morphology of the radial glia basal process. Throughout, we describe how dysregulation of these interactions and of basal process morphology can have profound effects on cortical development, and therefore lead to neurodevelopmental diseases.


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