Elsevier

NeuroImage

Volume 86, 1 February 2014, Pages 99-110
NeuroImage

Multimodal imaging of subventricular zone neural stem/progenitor cells in the cuprizone mouse model reveals increased neurogenic potential for the olfactory bulb pathway, but no contribution to remyelination of the corpus callosum

https://doi.org/10.1016/j.neuroimage.2013.07.080Get rights and content
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Highlights

  • Multimodal imaging of endogenous neural stem cell migration is feasible.

  • Cuprizone-induced inflammation enhances stem cell migration to the olfactory bulb.

  • Subventricular zone neural stem cells do not remyelinate cuprizone induced lesions.

Abstract

Multiple sclerosis is a devastating demyelinating disease of the central nervous system (CNS) in which endogenous remyelination, and thus recovery, often fails. Although the cuprizone mouse model allowed elucidation of many molecular factors governing remyelination, currently very little is known about the spatial origin of the oligodendrocyte progenitor cells that initiate remyelination in this model. Therefore, we here investigated in this model whether subventricular zone (SVZ) neural stem/progenitor cells (NSPCs) contribute to remyelination of the splenium following cuprizone-induced demyelination. Experimentally, from the day of in situ NSPC labeling, C57BL/6J mice were fed a 0.2% cuprizone diet during a 4-week period and then left to recover on a normal diet for 8 weeks. Two in situ labeling strategies were employed: (i) NSPCs were labeled by intraventricular injection of micron-sized iron oxide particles and then followed up longitudinally by means of magnetic resonance imaging (MRI), and (ii) SVZ NSPCs were transduced with a lentiviral vector encoding the eGFP and Luciferase reporter proteins for longitudinal monitoring by means of in vivo bioluminescence imaging (BLI). In contrast to preceding suggestions, no migration of SVZ NSPC towards the demyelinated splenium was observed using both MRI and BLI, and further validated by histological analysis, thereby demonstrating that SVZ NSPCs are unable to contribute directly to remyelination of the splenium in the cuprizone model. Interestingly, using longitudinal BLI analysis and confirmed by histological analysis, an increased migration of SVZ NSPC-derived neuroblasts towards the olfactory bulb was observed following cuprizone treatment, indicative for a potential link between CNS inflammation and increased neurogenesis.

Abbreviations

AP
antero-posterior
APC/CC1
adenomatous polyposis coli
BG
background
BLI
bioluminescence imaging
CC
corpus callosum
CNS
central nervous system
DV
dorso-ventral
EAE
experimental auto-immune encephalomyelitis
eGFP
enhanced green fluorescent protein
EWD
error weighted difference
fLuc
firefly luciferase
GE
gradient echo
GFAP
glial fibrillary acidic protein
IBA1
ionized calcium binding adaptor molecule
La
lateral
LVv
lentiviral vector
MBP
myelin basic protein
mIPs
minimum intensity projections
MPIO
micron-sized iron oxide particles
MRI
magnetic resonance imaging
MS
multiple sclerosis
NeuN
neuronal nuclear antigen
NSPC
neural stem progenitor cell
OB
olfactory bulb
p75NTR
p75 neurotrophin receptor
p.i.
post-injection
PBS
phosphate buffered saline
PC
positive control
PLL
poly-l-lysine
RF
radio-frequency
RMS
rostral migratory stream
ROI
region of interest
sCC
splenium of the corpus callosum
SVZ
subventricular zone
VOI
volume of interest

Keywords

Neural stem cell
Cuprizone
Migration
Remyelination
Magnetic resonance imaging
Bioluminescence imaging

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1

Both authors contributed equally to this study.