Modelling genetic reorganization in the mouse spinal cord affecting left-right coordination during locomotion

Research output: Contribution to journalJournal articleResearchpeer-review

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Modelling genetic reorganization in the mouse spinal cord affecting left-right coordination during locomotion. / Rybak, Ilya A.; Shevtsova, Natalia A.; Kiehn, Ole.

In: Journal of Physiology, Vol. 591, No. 22, 01.11.2013, p. 5491-5508.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Rybak, IA, Shevtsova, NA & Kiehn, O 2013, 'Modelling genetic reorganization in the mouse spinal cord affecting left-right coordination during locomotion', Journal of Physiology, vol. 591, no. 22, pp. 5491-5508. https://doi.org/10.1113/jphysiol.2013.261115

APA

Rybak, I. A., Shevtsova, N. A., & Kiehn, O. (2013). Modelling genetic reorganization in the mouse spinal cord affecting left-right coordination during locomotion. Journal of Physiology, 591(22), 5491-5508. https://doi.org/10.1113/jphysiol.2013.261115

Vancouver

Rybak IA, Shevtsova NA, Kiehn O. Modelling genetic reorganization in the mouse spinal cord affecting left-right coordination during locomotion. Journal of Physiology. 2013 Nov 1;591(22):5491-5508. https://doi.org/10.1113/jphysiol.2013.261115

Author

Rybak, Ilya A. ; Shevtsova, Natalia A. ; Kiehn, Ole. / Modelling genetic reorganization in the mouse spinal cord affecting left-right coordination during locomotion. In: Journal of Physiology. 2013 ; Vol. 591, No. 22. pp. 5491-5508.

Bibtex

@article{2b3452f9b94540e4bea43a780797631b,
title = "Modelling genetic reorganization in the mouse spinal cord affecting left-right coordination during locomotion",
abstract = "Abstract The spinal neural circuit contains inhibitory (CINi) and excitatory (CINe) commissural interneurons with axons crossing the mid-line. Direction of these axons to the other side of the cord is controlled by axon guidance molecules, such as Netrin-1 and DCC. The cord also contains glutamatergic interneurons, whose axon guidance involves the EphA4 receptor. In EphA4 knockout (KO) and Netrin-1 KO mice, the normal left-right alternating pattern is replaced with a synchronized hopping gait, and the cord of DCC KO mice exhibits uncoordinated left and right oscillations. To investigate the effects of these genetic transformations, we used a computational model of the spinal circuits containing left and right rhythm-generating neuron populations (RGs), each with a subpopulation of EphA4-positive neurons, and CINi and CINe populations mediating mutual inhibition and excitation between the left and right RGs. In the EphA4 KO circuits, half of the EphA4-positive axons crossed the mid-line and excited the contralateral RG neurons. In the Netrin-1 KO model, the number of contralateral CINi projections was significantly reduced, while in the DCC KO model, the numbers of both CINi and CINe connections were reduced. In our simulations, the EphA4 and Netrin-1 KO circuits switched from the left-right alternating pattern to a synchronized hopping pattern, and the DCC KO network exhibited uncoordinated left-right activity. The amplification of inhibitory interactions re-established an alternating pattern in the EphA4 and DCC KO circuits, but not in the Netrin-1 KO network. The model reproduces the genetic transformations and provides insights into the organization of the spinal locomotor network.",
author = "Rybak, {Ilya A.} and Shevtsova, {Natalia A.} and Ole Kiehn",
year = "2013",
month = nov,
day = "1",
doi = "10.1113/jphysiol.2013.261115",
language = "English",
volume = "591",
pages = "5491--5508",
journal = "The Journal of Physiology",
issn = "0022-3751",
publisher = "Wiley-Blackwell",
number = "22",

}

RIS

TY - JOUR

T1 - Modelling genetic reorganization in the mouse spinal cord affecting left-right coordination during locomotion

AU - Rybak, Ilya A.

AU - Shevtsova, Natalia A.

AU - Kiehn, Ole

PY - 2013/11/1

Y1 - 2013/11/1

N2 - Abstract The spinal neural circuit contains inhibitory (CINi) and excitatory (CINe) commissural interneurons with axons crossing the mid-line. Direction of these axons to the other side of the cord is controlled by axon guidance molecules, such as Netrin-1 and DCC. The cord also contains glutamatergic interneurons, whose axon guidance involves the EphA4 receptor. In EphA4 knockout (KO) and Netrin-1 KO mice, the normal left-right alternating pattern is replaced with a synchronized hopping gait, and the cord of DCC KO mice exhibits uncoordinated left and right oscillations. To investigate the effects of these genetic transformations, we used a computational model of the spinal circuits containing left and right rhythm-generating neuron populations (RGs), each with a subpopulation of EphA4-positive neurons, and CINi and CINe populations mediating mutual inhibition and excitation between the left and right RGs. In the EphA4 KO circuits, half of the EphA4-positive axons crossed the mid-line and excited the contralateral RG neurons. In the Netrin-1 KO model, the number of contralateral CINi projections was significantly reduced, while in the DCC KO model, the numbers of both CINi and CINe connections were reduced. In our simulations, the EphA4 and Netrin-1 KO circuits switched from the left-right alternating pattern to a synchronized hopping pattern, and the DCC KO network exhibited uncoordinated left-right activity. The amplification of inhibitory interactions re-established an alternating pattern in the EphA4 and DCC KO circuits, but not in the Netrin-1 KO network. The model reproduces the genetic transformations and provides insights into the organization of the spinal locomotor network.

AB - Abstract The spinal neural circuit contains inhibitory (CINi) and excitatory (CINe) commissural interneurons with axons crossing the mid-line. Direction of these axons to the other side of the cord is controlled by axon guidance molecules, such as Netrin-1 and DCC. The cord also contains glutamatergic interneurons, whose axon guidance involves the EphA4 receptor. In EphA4 knockout (KO) and Netrin-1 KO mice, the normal left-right alternating pattern is replaced with a synchronized hopping gait, and the cord of DCC KO mice exhibits uncoordinated left and right oscillations. To investigate the effects of these genetic transformations, we used a computational model of the spinal circuits containing left and right rhythm-generating neuron populations (RGs), each with a subpopulation of EphA4-positive neurons, and CINi and CINe populations mediating mutual inhibition and excitation between the left and right RGs. In the EphA4 KO circuits, half of the EphA4-positive axons crossed the mid-line and excited the contralateral RG neurons. In the Netrin-1 KO model, the number of contralateral CINi projections was significantly reduced, while in the DCC KO model, the numbers of both CINi and CINe connections were reduced. In our simulations, the EphA4 and Netrin-1 KO circuits switched from the left-right alternating pattern to a synchronized hopping pattern, and the DCC KO network exhibited uncoordinated left-right activity. The amplification of inhibitory interactions re-established an alternating pattern in the EphA4 and DCC KO circuits, but not in the Netrin-1 KO network. The model reproduces the genetic transformations and provides insights into the organization of the spinal locomotor network.

UR - http://www.scopus.com/inward/record.url?scp=84887615519&partnerID=8YFLogxK

U2 - 10.1113/jphysiol.2013.261115

DO - 10.1113/jphysiol.2013.261115

M3 - Journal article

C2 - 24081162

AN - SCOPUS:84887615519

VL - 591

SP - 5491

EP - 5508

JO - The Journal of Physiology

JF - The Journal of Physiology

SN - 0022-3751

IS - 22

ER -

ID: 194977176