Reversible silencing of lumbar spinal interneurons unmasks a task-specific network for securing hindlimb alternation.
Reversible silencing of lumbar spinal interneurons unmasks a task-specific network for securing hindlimb alternation.
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DOI:
10.1038/s41467-017-02033-x
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发表时间:
2017-12-06
影响因子:
16.6
通讯作者:
Magnuson DSK
中科院分区:
文献类型:
--
作者:
Pocratsky AM;Burke DA;Morehouse JR;Beare JE;Riegler AS;Tsoulfas P;States GJR;Whittemore SR;Magnuson DSK
Neural circuitry in the lumbar spinal cord governs two principal features of locomotion, rhythm and pattern, which reflect intra- and interlimb movement. These features are functionally organized into a hierarchy that precisely controls stepping in a stereotypic, speed-dependent fashion. Here, we show that a specific component of the locomotor pattern can be independently manipulated. Silencing spinal L2 interneurons that project to L5 selectively disrupts hindlimb alternation allowing a continuum of walking to hopping to emerge from the otherwise intact network. This perturbation, which is independent of speed and occurs spontaneously with each step, does not disrupt multi-joint movements or forelimb alternation, nor does it translate to a non-weight-bearing locomotor activity. Both the underlying rhythm and the usual relationship between speed and spatiotemporal characteristics of stepping persist. These data illustrate that hindlimb alternation can be manipulated independently from other core features of stepping, revealing a striking freedom in an otherwise precisely controlled system. Intra- and interlimb coordination during locomotion is governed by hierarchically organized lumbar spinal networks. Here, the authors show that reversible silencing of spinal L2–L5 interneurons specifically disrupts hindlimb alternation leading to a continuum of walking to hopping.
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DOI:
10.1073/pnas.1419045111
发表时间:
2014-11-25
影响因子:
11.1
作者:
Akay, Turgay;Tourtellotte, Warren G.;Jessell, Thomas M.
通讯作者:
Jessell, Thomas M.
影响因子:
2.5
作者:
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通讯作者:
Schmidt, BJ
影响因子:
5.3
作者:
Dougherty, Kimberly J.;Kiehn, Ole
通讯作者:
Kiehn, Ole
影响因子:
16.2
作者:
Fremeau, RT;Troyer, MD;Edwards, RH
通讯作者:
Edwards, RH
影响因子:
--
作者:
Butt, SJB;Lebret, JM;Kiehn, O
通讯作者:
Kiehn, O