2015
DOI: 10.1002/glia.22929
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GPR17 expressing NG2‐Glia: Oligodendrocyte progenitors serving as a reserve pool after injury

Abstract: In the adult brain NG2-glia continuously generate mature, myelinating oligodendrocytes. To which extent the differentiation process is common to all NG2-glia and whether distinct pools are recruited for repair under physiological and pathological conditions still needs clarification. Here, we aimed at investigating the differentiation potential of adult NG2-glia that specifically express the G-protein coupled receptor 17 (GPR17), a membrane receptor that regulates the differentiation of these cells at postnata… Show more

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Cited by 69 publications
(101 citation statements)
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References 30 publications
(100 reference statements)
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“…Following chronic stress, NG2-glia have been shown to upregulate death receptor 6 expression, a TNFα receptor upstream of JNK and NF-κB pathways [106]. (3) G-coupled protein 17 (GFPR17) expressed by a subset of NG2-glia has also been suggested to act as a molecular sensor to environmental insults [107] and might play a role in stress sensing in the adult CNS. (4) GSK3 is a fundamental signaling hub in oligodendrocytes which integrates key processes as metabolism, inflammation and myelination [108].…”
Section: Association Of Ng2-glia With Neuropsychiatric Disordersmentioning
confidence: 99%
“…Following chronic stress, NG2-glia have been shown to upregulate death receptor 6 expression, a TNFα receptor upstream of JNK and NF-κB pathways [106]. (3) G-coupled protein 17 (GFPR17) expressed by a subset of NG2-glia has also been suggested to act as a molecular sensor to environmental insults [107] and might play a role in stress sensing in the adult CNS. (4) GSK3 is a fundamental signaling hub in oligodendrocytes which integrates key processes as metabolism, inflammation and myelination [108].…”
Section: Association Of Ng2-glia With Neuropsychiatric Disordersmentioning
confidence: 99%
“…Importantly, GPR17-expressing OPCs serve as a reserve pool for tissue repair after brain damage (15). GPR17-positive OPCs rapidly react to the damage and undergo maturation in a mouse model of cerebral injury and ischemia (15).…”
Section: Quantification Of Gpr17 Immunoreactive Cellsmentioning
confidence: 99%
“…GPR17-positive OPCs rapidly react to the damage and undergo maturation in a mouse model of cerebral injury and ischemia (15). The GPR17 agonist UDP-glucose promotes the recovery of myelination in ischemic periventricular leukomalacia (PVL), a rat model of cerebral white matter injury (16), suggesting that GPR17 activation facilitates myelination in vivo.…”
Section: Quantification Of Gpr17 Immunoreactive Cellsmentioning
confidence: 99%
“…For example, GPR126/ ADGRG6 could be targeted in the PNS, perhaps by a modified Stachel-sequence peptide [20], to promote myelination in MDC1A, as these patients lack functional laminin-211 ligand but should possess GPR126/ADGRG6 in Schwann cells. In the CNS, Gpr17 has been explored as a potential therapeutic target in remyelination either by inhibiting Gpr17 via antagonists or by activating the reserve pool of Gpr17-expressing OPCs to maturation [79,80]. As Gpr17 is enriched in white matter plaques of MS patients and in rodent models of MS, antagonism of Gpr17 or other inhibitory GPCRs may indeed be efficacious in future treatment strategies [57,64,66,67].…”
mentioning
confidence: 99%