arrow
Return

Cerebellar nuclei excitatory neurons regulate developmental scaling of presynaptic Purkinje cell number and organ growth

delete2019-11-19
delete32
delete
OA
AI
R
Ryan T. Willett
N
N. Sumru Bayın
A
Andrew S. Lee
A
Anjana Krishnamurthy
A
Alexandre Wojcinski
Z
Zhimin Lao
D
Daniel Stephen
A
Alberto Roselló‐Díez
K
Katherine L Dauber-Decker
G
Grant D. Orvis
Z
Zhuhao Wu
M
Marc Tessier‐Lavigne
A
Alexandra L. Joyner *
DOI:10.7554/eLife.50617delete
deleteOriginal
deleteOriginal request for help
deleteShare
deleteSave
Abstract

Abstract

En 中文
For neural systems to function effectively, the numbers of each cell type must be proportioned properly during development. We found that conditional knockout of the mouse homeobox genes En1 and En2 in the excitatory cerebellar nuclei neurons (eCN) leads to reduced postnatal growth of the cerebellar cortex. A subset of medial and intermediate eCN are lost in the mutants, with an associated cell non-autonomous loss of their presynaptic partner Purkinje cells by birth leading to proportional scaling down of neuron production in the postnatal cerebellar cortex. Genetic killing of embryonic eCN throughout the cerebellum also leads to loss of Purkinje cells and reduced postnatal growth but throughout the cerebellar cortex. Thus, the eCN play a key role in scaling the size of the cerebellum by influencing the survival of their Purkinje cell partners, which in turn regulate production of granule cells and interneurons via the amount of sonic hedgehog secreted.
Keywords:
ENGRAILED HOMEOBOX GENES
EXPRESSION
REVEALS
MOUSE
DIFFERENTIATION
FOLIATION
LINEAGES
SURVIVAL
MICE
NEUROTROPHINS

Journal

eLife cover
eLife
IF:
0
Papers:
1.8W
Citations:
16

Organization

R
rockefeller university
Scholars:
6.6K
Papers: 4.9K
Citations: 15
M
Memorial Sloan Kettering Cancer Center
Scholars:
3.4W
Papers: 2.4W
Citations: 4.6W