The olfactory conditioning in the early postnatal period stimulated neural stem/progenitor cells in the subventricular zone and increased neurogenesis in the olfactory bulb of rats

Neuroscience ◽  
2008 ◽  
Vol 151 (1) ◽  
pp. 120-128 ◽  
Author(s):  
K. So ◽  
T. Moriya ◽  
S. Nishitani ◽  
H. Takahashi ◽  
K. Shinohara
2016 ◽  
Vol 38 (6) ◽  
pp. 430-444 ◽  
Author(s):  
William J. Dawes ◽  
Xinyu Zhang ◽  
Stephen P.J. Fancy ◽  
David Rowitch ◽  
Silvia Marino

Precise temporal and spatial control of the neural stem/progenitor cells within the subventricular zone (SVZ) germinal matrix of the brain is important for normal development in the third trimester and the early postnatal period. The high metabolic demands of proliferating germinal matrix precursors, coupled with the flimsy structure of the germinal matrix cerebral vasculature, are thought to account for the high rates of haemorrhage in extremely- and very-low-birth-weight preterm infants. Germinal matrix haemorrhage can commonly extend to intraventricular haemorrhage (IVH). Because neural stem/progenitor cells are sensitive to microenvironmental cues from the ventricular, intermediate, and basal domains within the germinal matrix, haemorrhage has been postulated to impact neurological outcomes through aberration of normal neural stem/progenitor cell behaviour. We developed an animal model of neonatal germinal matrix haemorrhage using stereotactic injection of autologous blood into the mouse neonatal germinal matrix. Pathological analysis at 4 days postinjury showed high rates of intraventricular extension and ventricular dilatation but low rates of parenchymal disruption outside the germinal zone, recapitulating key features of human “Papile grade III” IVH. At 4 days postinjury we observed proliferation in the wall of the lateral ventricle with significantly increased numbers of transient amplifying cells within the SVZ and the corpus callosum. Analysis at 21 days postinjury revealed that cortical development was also affected, with increased neuronal and concomitant reduced oligodendroglial differentiation. At the molecular level, we showed downregulation of the expression of the transmembrane receptor Notch2 in CD133+ve cells of the SVZ, raising the possibility that the burst of precocious proliferation seen in our experimental mouse model and the skewed differentiation could be mediated by downregulation of the Notch pathway within the proximal/ventricular domain. These findings raise the possibility that Notch regulation plays a critical role in mediating the response of the neonatal SVZ to ischaemic and haemorrhagic insults.


2020 ◽  
Vol 15 (10) ◽  
pp. 1773 ◽  
Author(s):  
Giuseppe Lupo ◽  
Giancarlo Poiana ◽  
Roberta Gioia ◽  
Serena Sineri ◽  
Silvia Cardarelli ◽  
...  

2015 ◽  
Vol 93 (8) ◽  
pp. 1203-1214 ◽  
Author(s):  
Chiara Soldati ◽  
Pasquale Caramanica ◽  
Matthew J. Burney ◽  
Camilla Toselli ◽  
Angela Bithell ◽  
...  

2019 ◽  
Vol 29 (11) ◽  
pp. 4831-4849 ◽  
Author(s):  
Teng Guo ◽  
Guoping Liu ◽  
Heng Du ◽  
Yan Wen ◽  
Song Wei ◽  
...  

Abstract Generation of olfactory bulb (OB) interneurons requires neural stem/progenitor cell specification, proliferation, differentiation, and young interneuron migration and maturation. Here, we show that the homeobox transcription factors Dlx1/2 are central and essential components in the transcriptional code for generating OB interneurons. In Dlx1/2 constitutive null mutants, the differentiation of GSX2+ and ASCL1+ neural stem/progenitor cells in the dorsal lateral ganglionic eminence is blocked, resulting in a failure of OB interneuron generation. In Dlx1/2 conditional mutants (hGFAP-Cre; Dlx1/2F/− mice), GSX2+ and ASCL1+ neural stem/progenitor cells in the postnatal subventricular zone also fail to differentiate into OB interneurons. In contrast, overexpression of Dlx1&2 in embryonic mouse cortex led to ectopic production of OB-like interneurons that expressed Gad1, Sp8, Sp9, Arx, Pbx3, Etv1, Tshz1, and Prokr2. Pax6 mutants generate cortical ectopia with OB-like interneurons, but do not do so in compound Pax6; Dlx1/2 mutants. We propose that DLX1/2 promote OB interneuron development mainly through activating the expression of Sp8/9, which further promote Tshz1 and Prokr2 expression. Based on this study, in combination with earlier ones, we propose a transcriptional network for the process of OB interneuron development.


2014 ◽  
Vol 225 ◽  
pp. 81-89 ◽  
Author(s):  
Hadi Aligholi ◽  
Gholamreza Hassanzadeh ◽  
Hassan Azari ◽  
Seyed Mahdi Rezayat ◽  
Shahram Ejtemaei Mehr ◽  
...  

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