TY - JOUR
T1 - A Dynamic Unfolded Protein Response Contributes to the Control of Cortical Neurogenesis
AU - Laguesse, Sophie
AU - Creppe, Catherine
AU - Nedialkova, Danny D.
AU - Prévot, Pierre Paul
AU - Borgs, Laurence
AU - Huysseune, Sandra
AU - Franco, Bénédicte
AU - Duysens, Guérin
AU - Krusy, Nathalie
AU - Lee, Gabsang
AU - Thelen, Nicolas
AU - Thiry, Marc
AU - Close, Pierre
AU - Chariot, Alain
AU - Malgrange, Brigitte
AU - Leidel, Sebastian A.
AU - Godin, Juliette D.
AU - Nguyen, Laurent
N1 - Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015
Y1 - 2015
N2 - The cerebral cortex contains layers of neurons sequentially generated by distinct lineage-related progenitors. At the onset of corticogenesis, the first-born progenitors are apical progenitors (APs), whose asymmetric division gives birth directly to neurons. Later, they switch to indirect neurogenesis by generating intermediate progenitors (IPs), which give rise to projection neurons of all cortical layers. While a direct lineage relationship between APs and IPs has been established, the molecular mechanism that controls their transition remains elusive. Here we show that interfering with codon translation speed triggers ER stress and the unfolded protein response (UPR), further impairing the generation of IPs and leading to microcephaly. Moreover, we demonstrate that a progressive downregulation of UPR in cortical progenitors acts as a physiological signal to amplify IPs and promotes indirect neurogenesis. Thus, our findings reveal a contribution of UPR to cell fate acquisition during mammalian brain development.
AB - The cerebral cortex contains layers of neurons sequentially generated by distinct lineage-related progenitors. At the onset of corticogenesis, the first-born progenitors are apical progenitors (APs), whose asymmetric division gives birth directly to neurons. Later, they switch to indirect neurogenesis by generating intermediate progenitors (IPs), which give rise to projection neurons of all cortical layers. While a direct lineage relationship between APs and IPs has been established, the molecular mechanism that controls their transition remains elusive. Here we show that interfering with codon translation speed triggers ER stress and the unfolded protein response (UPR), further impairing the generation of IPs and leading to microcephaly. Moreover, we demonstrate that a progressive downregulation of UPR in cortical progenitors acts as a physiological signal to amplify IPs and promotes indirect neurogenesis. Thus, our findings reveal a contribution of UPR to cell fate acquisition during mammalian brain development.
UR - http://www.scopus.com/inward/record.url?scp=84961576051&partnerID=8YFLogxK
U2 - 10.1016/j.devcel.2015.11.005
DO - 10.1016/j.devcel.2015.11.005
M3 - Article
C2 - 26651292
AN - SCOPUS:84961576051
SN - 1534-5807
VL - 35
SP - 553
EP - 567
JO - Developmental Cell
JF - Developmental Cell
IS - 5
ER -