2014
DOI: 10.1002/glia.22674
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Neurotransmitter signaling in white matter

Abstract: White matter (WM) tracts are bundles of myelinated axons that provide for rapid communication throughout the CNS and integration in grey matter (GM). The main cells in myelinated tracts are oligodendrocytes and astrocytes, with small populations of microglia and oligodendrocyte precursor cells. The prominence of neurotransmitter signaling in WM, which largely exclude neuronal cell bodies, indicates it must have physiological functions other than neuron-to-neuron communication. A surprising aspect is the divers… Show more

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Cited by 108 publications
(89 citation statements)
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“…Action potential-induced sodium increases in corpus callosum macroglial cells were strongly reduced by combined inhibition of glutamate receptors and glutamate transport, indicating that they are largely related to release of glutamate. This is in line with numerous earlier reports suggesting that active axons release glutamate into the periaxonal space (e.g., [16][17][18][19]26]). In addition, there is evidence that glutamate is also released by astrocytes [19].…”
Section: Action Potentials Induce Sodium Transients In White Matter Gsupporting
confidence: 93%
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“…Action potential-induced sodium increases in corpus callosum macroglial cells were strongly reduced by combined inhibition of glutamate receptors and glutamate transport, indicating that they are largely related to release of glutamate. This is in line with numerous earlier reports suggesting that active axons release glutamate into the periaxonal space (e.g., [16][17][18][19]26]). In addition, there is evidence that glutamate is also released by astrocytes [19].…”
Section: Action Potentials Induce Sodium Transients In White Matter Gsupporting
confidence: 93%
“…In addition to glutamate transporters, white matter macroglia express a large repertoire of receptors for different transmitters [26,27]. Their activation upon action potential (AP) propagation triggers calcium signals in astrocytes in the optic nerve and corpus callosum, involving both glutamate and purine receptors [19,[28][29][30].…”
Section: Introductionmentioning
confidence: 99%
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“…Thus, numerous studies conducted in cellular and animal models of MS, as well as in post-mortem brain and in patients, indicate that excitotoxicity mediated by Ca 2+ -permeable glutamate receptors contributes to oligodendrocyte death, demyelination, and tissue damage in MS [43]. In particular, experimental MS is alleviated by α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) and kainate receptor antagonists, but not N-methyl-d-aspartate receptor blockade, and combination with anti-inflammatory agents expands neuroprotection even at advanced disease stages [44].…”
Section: Potential Therapiesmentioning
confidence: 99%
“…Moreover, genome-wide association screening associated alleles in AMPA receptor genes in MS patients to brain volume loss in patients with high glutamate levels [45]. In turn, glutamate levels are increased in the brain in MS as a consequence of reduced expression of the glutamate transporters (excitatory amino acid transporters 1 and 2) and upregulation of the cystine/glutamate antiporter in the monocyte-macrophage-microglia lineage is associated with immune activation in both MS and experimental autoimmune encephalomyelitis (EAE) [43,46]. Like glutamate, ATP, when in excess, is a potent endogenous toxin that can directly kill oligodendrocytes via activation of purinergic P2X7 receptors whose blockade during the chronic phase of EAE attenuates the symptoms and tissue damage [47].…”
Section: Potential Therapiesmentioning
confidence: 99%