Probing circuits for spinal motor control

Spinal circuits can generate locomotor output in the absence of sensory or descending input, but the principles of locomotor circuit organization remain unclear. We sought insight into these principles by considering the elaboration of locomotor circuits across evolution. The identity of limb-innerv...

Full description

Bibliographic Details
Main Author: Machado, Timothy Aloysius
Language:English
Published: 2015
Subjects:
Online Access:https://doi.org/10.7916/D8TT4Q8J
id ndltd-columbia.edu-oai-academiccommons.columbia.edu-10.7916-D8TT4Q8J
record_format oai_dc
spelling ndltd-columbia.edu-oai-academiccommons.columbia.edu-10.7916-D8TT4Q8J2019-05-09T15:14:55ZProbing circuits for spinal motor controlMachado, Timothy Aloysius2015ThesesNeurosciencesSpinal circuits can generate locomotor output in the absence of sensory or descending input, but the principles of locomotor circuit organization remain unclear. We sought insight into these principles by considering the elaboration of locomotor circuits across evolution. The identity of limb-innervating motor neurons was reverted to a state resembling that of motor neurons that direct undulatory swimming in primitive aquatic vertebrates, permitting assessment of the role of motor neuron identity in determining locomotor pattern. Two-photon imaging was coupled with spike inference to measure locomotor firing in hundreds of motor neurons in isolated mouse spinal cords. In wild type preparations we observed sequential recruitment of motor neurons innervating flexor muscles controlling progressively more distal joints. Strikingly, after reversion of motor neuron identity virtually all firing patterns became distinctly flexor-like. Our interneuron imaging experiments demonstrate a new approach for functionally mapping the types of inputs that motor neurons might receive during locomotor firing. These data revealed that En1-derived inhibitory spinal interneuron activity appears to be dominated by a flexor-like pattern across the ventrolateral extent of the lumbar spinal cord–even in the regions surrounding flexor and extensor motor pools. Together, these findings show that motor neuron identity directs locomotor circuit wiring, and indicate the evolutionary primacy of flexor pattern generation.Englishhttps://doi.org/10.7916/D8TT4Q8J
collection NDLTD
language English
sources NDLTD
topic Neurosciences
spellingShingle Neurosciences
Machado, Timothy Aloysius
Probing circuits for spinal motor control
description Spinal circuits can generate locomotor output in the absence of sensory or descending input, but the principles of locomotor circuit organization remain unclear. We sought insight into these principles by considering the elaboration of locomotor circuits across evolution. The identity of limb-innervating motor neurons was reverted to a state resembling that of motor neurons that direct undulatory swimming in primitive aquatic vertebrates, permitting assessment of the role of motor neuron identity in determining locomotor pattern. Two-photon imaging was coupled with spike inference to measure locomotor firing in hundreds of motor neurons in isolated mouse spinal cords. In wild type preparations we observed sequential recruitment of motor neurons innervating flexor muscles controlling progressively more distal joints. Strikingly, after reversion of motor neuron identity virtually all firing patterns became distinctly flexor-like. Our interneuron imaging experiments demonstrate a new approach for functionally mapping the types of inputs that motor neurons might receive during locomotor firing. These data revealed that En1-derived inhibitory spinal interneuron activity appears to be dominated by a flexor-like pattern across the ventrolateral extent of the lumbar spinal cord–even in the regions surrounding flexor and extensor motor pools. Together, these findings show that motor neuron identity directs locomotor circuit wiring, and indicate the evolutionary primacy of flexor pattern generation.
author Machado, Timothy Aloysius
author_facet Machado, Timothy Aloysius
author_sort Machado, Timothy Aloysius
title Probing circuits for spinal motor control
title_short Probing circuits for spinal motor control
title_full Probing circuits for spinal motor control
title_fullStr Probing circuits for spinal motor control
title_full_unstemmed Probing circuits for spinal motor control
title_sort probing circuits for spinal motor control
publishDate 2015
url https://doi.org/10.7916/D8TT4Q8J
work_keys_str_mv AT machadotimothyaloysius probingcircuitsforspinalmotorcontrol
_version_ 1719046556813885440