Endogenous GABA controls oligodendrocyte lineage cell number, myelination, and CNS internode length

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Endogenous GABA controls oligodendrocyte lineage cell number, myelination, and CNS internode length. / Hamilton, Nicola B; Clarke, Laura E; Arancibia-Carcamo, I Lorena; Kougioumtzidou, Eleni; Matthey, Moritz; Káradóttir, Ragnhildur; Whiteley, Louise; Bergersen, Linda H; Richardson, William D; Attwell, David.

In: Glia, Vol. 65, No. 2, 02.2017, p. 309–321 .

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hamilton, NB, Clarke, LE, Arancibia-Carcamo, IL, Kougioumtzidou, E, Matthey, M, Káradóttir, R, Whiteley, L, Bergersen, LH, Richardson, WD & Attwell, D 2017, 'Endogenous GABA controls oligodendrocyte lineage cell number, myelination, and CNS internode length', Glia, vol. 65, no. 2, pp. 309–321 . https://doi.org/10.1002/glia.23093

APA

Hamilton, N. B., Clarke, L. E., Arancibia-Carcamo, I. L., Kougioumtzidou, E., Matthey, M., Káradóttir, R., Whiteley, L., Bergersen, L. H., Richardson, W. D., & Attwell, D. (2017). Endogenous GABA controls oligodendrocyte lineage cell number, myelination, and CNS internode length. Glia, 65(2), 309–321 . https://doi.org/10.1002/glia.23093

Vancouver

Hamilton NB, Clarke LE, Arancibia-Carcamo IL, Kougioumtzidou E, Matthey M, Káradóttir R et al. Endogenous GABA controls oligodendrocyte lineage cell number, myelination, and CNS internode length. Glia. 2017 Feb;65(2):309–321 . https://doi.org/10.1002/glia.23093

Author

Hamilton, Nicola B ; Clarke, Laura E ; Arancibia-Carcamo, I Lorena ; Kougioumtzidou, Eleni ; Matthey, Moritz ; Káradóttir, Ragnhildur ; Whiteley, Louise ; Bergersen, Linda H ; Richardson, William D ; Attwell, David. / Endogenous GABA controls oligodendrocyte lineage cell number, myelination, and CNS internode length. In: Glia. 2017 ; Vol. 65, No. 2. pp. 309–321 .

Bibtex

@article{0c07f57aff22478994e4cb13a864d692,
title = "Endogenous GABA controls oligodendrocyte lineage cell number, myelination, and CNS internode length",
abstract = "Adjusting the thickness and internodal length of the myelin sheath is a mechanism for tuning the conduction velocity of axons to match computational needs. Interactions between oligodendrocyte precursor cells (OPCs) and developing axons regulate the formation of myelin around axons. We now show, using organotypic cerebral cortex slices from mice expressing eGFP in Sox10-positive oligodendrocytes, that endogenously released GABA, acting on GABAA receptors, greatly reduces the number of oligodendrocyte lineage cells. The decrease in oligodendrocyte number correlates with a reduction in the amount of myelination but also an increase in internode length, a parameter previously thought to be set by the axon diameter or to be a property intrinsic to oligodendrocytes. Importantly, while TTX block of neuronal activity had no effect on oligodendrocyte lineage cell number when applied alone, it was able to completely abolish the effect of blocking GABAA receptors, suggesting that control of myelination by endogenous GABA may require a permissive factor to be released from axons. In contrast, block of AMPA/KA receptors had no effect on oligodendrocyte lineage cell number or myelination. These results imply that, during development, GABA can act as a local environmental cue to control myelination and thus influence the conduction velocity of action potentials within the CNS.",
author = "Hamilton, {Nicola B} and Clarke, {Laura E} and Arancibia-Carcamo, {I Lorena} and Eleni Kougioumtzidou and Moritz Matthey and Ragnhildur K{\'a}rad{\'o}ttir and Louise Whiteley and Bergersen, {Linda H} and Richardson, {William D} and David Attwell",
note = "{\textcopyright} 2016 The Authors Glia Published by Wiley Periodicals, Inc.",
year = "2017",
month = feb,
doi = "10.1002/glia.23093",
language = "English",
volume = "65",
pages = "309–321 ",
journal = "GLIA",
issn = "0894-1491",
publisher = "JohnWiley & Sons, Inc.",
number = "2",

}

RIS

TY - JOUR

T1 - Endogenous GABA controls oligodendrocyte lineage cell number, myelination, and CNS internode length

AU - Hamilton, Nicola B

AU - Clarke, Laura E

AU - Arancibia-Carcamo, I Lorena

AU - Kougioumtzidou, Eleni

AU - Matthey, Moritz

AU - Káradóttir, Ragnhildur

AU - Whiteley, Louise

AU - Bergersen, Linda H

AU - Richardson, William D

AU - Attwell, David

N1 - © 2016 The Authors Glia Published by Wiley Periodicals, Inc.

PY - 2017/2

Y1 - 2017/2

N2 - Adjusting the thickness and internodal length of the myelin sheath is a mechanism for tuning the conduction velocity of axons to match computational needs. Interactions between oligodendrocyte precursor cells (OPCs) and developing axons regulate the formation of myelin around axons. We now show, using organotypic cerebral cortex slices from mice expressing eGFP in Sox10-positive oligodendrocytes, that endogenously released GABA, acting on GABAA receptors, greatly reduces the number of oligodendrocyte lineage cells. The decrease in oligodendrocyte number correlates with a reduction in the amount of myelination but also an increase in internode length, a parameter previously thought to be set by the axon diameter or to be a property intrinsic to oligodendrocytes. Importantly, while TTX block of neuronal activity had no effect on oligodendrocyte lineage cell number when applied alone, it was able to completely abolish the effect of blocking GABAA receptors, suggesting that control of myelination by endogenous GABA may require a permissive factor to be released from axons. In contrast, block of AMPA/KA receptors had no effect on oligodendrocyte lineage cell number or myelination. These results imply that, during development, GABA can act as a local environmental cue to control myelination and thus influence the conduction velocity of action potentials within the CNS.

AB - Adjusting the thickness and internodal length of the myelin sheath is a mechanism for tuning the conduction velocity of axons to match computational needs. Interactions between oligodendrocyte precursor cells (OPCs) and developing axons regulate the formation of myelin around axons. We now show, using organotypic cerebral cortex slices from mice expressing eGFP in Sox10-positive oligodendrocytes, that endogenously released GABA, acting on GABAA receptors, greatly reduces the number of oligodendrocyte lineage cells. The decrease in oligodendrocyte number correlates with a reduction in the amount of myelination but also an increase in internode length, a parameter previously thought to be set by the axon diameter or to be a property intrinsic to oligodendrocytes. Importantly, while TTX block of neuronal activity had no effect on oligodendrocyte lineage cell number when applied alone, it was able to completely abolish the effect of blocking GABAA receptors, suggesting that control of myelination by endogenous GABA may require a permissive factor to be released from axons. In contrast, block of AMPA/KA receptors had no effect on oligodendrocyte lineage cell number or myelination. These results imply that, during development, GABA can act as a local environmental cue to control myelination and thus influence the conduction velocity of action potentials within the CNS.

U2 - 10.1002/glia.23093

DO - 10.1002/glia.23093

M3 - Journal article

C2 - 27796063

VL - 65

SP - 309

EP - 321

JO - GLIA

JF - GLIA

SN - 0894-1491

IS - 2

ER -

ID: 168877242