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About:
The interleukin-4/PPARγ signaling axis promotes oligodendrocyte differentiation and remyelination after brain injury
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covidontheweb.inria.fr
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Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
The interleukin-4/PPARγ signaling axis promotes oligodendrocyte differentiation and remyelination after brain injury
Creator
Chen, Jun
Cai, Wei
Dai, Xuejiao
Gao, Yanqin
Liu, Xiangrong
Mu, Hongfeng
Shi, Ligen
Xu, Fei
Zhang, Qingxiu
Zhu, Wen
Chenid, Jie
Foleyid, Lesley
Hitchensid, T
Huid, Xiaoming
Leakid, Rehana
Shiid, Yejie
Source
PMC
abstract
The repair of white matter damage is of paramount importance for functional recovery after brain injuries. Here, we report that interleukin-4 (IL-4) promotes oligodendrocyte regeneration and remyelination. IL-4 receptor expression was detected in a variety of glial cells after ischemic brain injury, including oligodendrocyte lineage cells. IL-4 deficiency in knockout mice resulted in greater deterioration of white matter over 14 d after stroke. Consistent with these findings, intranasal delivery of IL-4 nanoparticles after stroke improved white matter integrity and attenuated long-term sensorimotor and cognitive deficits in wild-type mice, as revealed by histological immunostaining, electron microscopy, diffusion tensor imaging, and electrophysiology. The selective effect of IL-4 on remyelination was verified in an ex vivo organotypic model of demyelination. By leveraging primary oligodendrocyte progenitor cells (OPCs), microglia-depleted mice, and conditional OPC-specific peroxisome proliferator-activated receptor gamma (PPARγ) knockout mice, we discovered a direct salutary effect of IL-4 on oligodendrocyte differentiation that was mediated by the PPARγ axis. Our findings reveal a new regenerative role of IL-4 in the central nervous system (CNS), which lies beyond its known immunoregulatory functions on microglia/macrophages or peripheral lymphocytes. Therefore, intranasal IL-4 delivery may represent a novel therapeutic strategy to improve white matter integrity in stroke and other brain injuries.
has issue date
2019-06-21
(
xsd:dateTime
)
bibo:doi
10.1371/journal.pbio.3000330
bibo:pmid
31226122
has license
cc-by
sha1sum (hex)
5719934f2cd95ffe4bd1aec0b7b9a314481aab60
schema:url
https://doi.org/10.1371/journal.pbio.3000330
resource representing a document's title
The interleukin-4/PPARγ signaling axis promotes oligodendrocyte differentiation and remyelination after brain injury
has PubMed Central identifier
PMC6608986
has PubMed identifier
31226122
schema:publication
PLoS Biol
resource representing a document's body
covid:5719934f2cd95ffe4bd1aec0b7b9a314481aab60#body_text
is
schema:about
of
named entity 'white matter'
named entity 'cognitive deficits'
named entity 'model'
named entity 'knockout mice'
named entity 'paramount'
named entity 'revealed'
named entity 'detected'
named entity 'histological'
named entity 'glial cells'
named entity 'discovered'
named entity 'AXIS'
covid:arg/5719934f2cd95ffe4bd1aec0b7b9a314481aab60
named entity 'WHITE MATTER INTEGRITY'
named entity 'REGENERATIVE'
named entity 'HERE'
named entity 'ROLE'
named entity 'GLIAL CELLS'
named entity 'REPRESENT'
named entity 'SELECTIVE'
named entity 'ISCHEMIC BRAIN INJURY'
named entity 'STROKE'
named entity 'LONG-TERM'
named entity 'CONSISTENT WITH'
named entity 'DELIVERY'
named entity 'ATTENUATED'
named entity 'MICE'
named entity 'WILD-TYPE'
named entity 'REPORT'
named entity 'EX VIVO'
named entity 'ORGANOTYPIC'
named entity 'DETECTED'
named entity 'VARIETY'
named entity 'MEDIATED'
named entity 'KNOCKOUT MICE'
named entity 'LINEAGE'
named entity 'DAMAGE'
named entity 'DETERIORATION'
named entity 'STRATEGY'
named entity 'INTERLEUKIN-4 '
named entity 'NOVEL'
named entity 'ITS'
named entity 'OLIGODENDROCYTE'
named entity 'HISTOLOGICAL'
named entity 'REPAIR'
named entity 'DEPLETED'
named entity 'RECEPTOR'
named entity 'LYMPHOCYTES'
named entity 'OLIGODENDROCYTE DIFFERENTIATION'
named entity 'BEYOND'
named entity 'VERIFIED'
named entity 'IL-4 RECEPTOR'
named entity 'FUNCTIONAL RECOVERY'
named entity 'OUR'
named entity 'FUNCTIONS'
named entity 'BRAIN INJURY'
named entity 'AXIS'
named entity 'DEFICIENCY'
named entity 'NANOPARTICLES'
named entity 'IMPROVED'
named entity 'REVEALED'
named entity 'PRIMARY'
named entity 'CELLS'
named entity 'SPECIFIC'
named entity 'DIRECT'
named entity 'KNOWN'
named entity 'INCLUDING'
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