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Evolution of the vertebrate motor system - from forebrain to spinal cord

Grillner, Sten·2021·Current Opinion in Neurobiology

Abstract

A comparison of the vertebrate motor systems of the oldest group of now living vertebrates (lamprey) with that of mammals shows that there are striking similarities not only in the basic organization but also with regard to synaptic properties, transmitters and neuronal properties. The lamprey dorsal pallium (cortex) has a motor, a visual and a somatosensory area, and the basal ganglia, including the dopamine system, are organized in a virtually identical way in the lamprey and rodents. This also applies to the midbrain, brainstem and spinal cord. However, during evolution additional capabilities such as systems for the control of foreleg/arms, hands and fingers have evolved. The findings suggest that when the evolutionary lineages of mammals and lamprey became separate around 500 million years ago, the blueprint of the vertebrate motor system had already evolved.

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  1. Zega, 2006, Development of swimming behaviour in the larva of the ascidian Ciona intestinalis, J Exp Biol, 209, 3405, 10.1242/jeb.02421 · DOI
  2. Arendt, 2021, Elementary nervous systems, Philos Trans R Soc Lond B Biol Sci, 376, 20200347, 10.1098/rstb.2020.0347 · DOI
  3. Horie, 2018, Shared evolutionary origin of vertebrate neural crest and cranial placodes, Nature, 560, 228, 10.1038/s41586-018-0385-7 · DOI
  4. Lacalli, 2018, Amphioxus, motion detection, and the evolutionary origin of the vertebrate retinotectal map, Evodevo, 9, 6, 10.1186/s13227-018-0093-2 · DOI
  5. Grillner, 2006, Biological pattern generation: the cellular and computational logic of networks in motion, Neuron, 52, 751, 10.1016/j.neuron.2006.11.008 · DOI
  6. Grillner, 2016, The basal ganglia over 500 million years, Curr Biol, 26, R1088, 10.1016/j.cub.2016.06.041 · DOI
  7. Suryanarayana, 2020, The evolutionary origin of visual and somatosensory representation in the vertebrate pallium, Nat Ecol Evol, 4, 639, 10.1038/s41559-020-1137-2 · DOI
  8. Fournier, 2018, Spatial information in a non-retinotopic visual cortex, Neuron, 97, 164, 10.1016/j.neuron.2017.11.017 · DOI
  9. Manger, 2002, Visual subdivisions of the dorsal ventricular ridge of the iguana (Iguana iguana) as determined by electrophysiologic mapping, J Comp Neurol, 453, 226, 10.1002/cne.10373 · DOI
  10. Ocaña, 2015, The lamprey pallium provides a blueprint of the mammalian motor projections from cortex, Curr Biol, 25, 413, 10.1016/j.cub.2014.12.013 · DOI
  11. Suryanarayana, 2017, The lamprey pallium provides a blueprint of the mammalian layered cortex, Curr Biol, 27, 3264, 10.1016/j.cub.2017.09.034 · DOI
  12. Suryanarayana, 2021, Olfaction in lamprey pallium revisited-dual projections of mitral and tufted cells, Cell Rep, 34, 108596, 10.1016/j.celrep.2020.108596 · DOI
  13. Tasic, 2018, Shared and distinct transcriptomic cell types across neocortical areas, Nature, 563, 72, 10.1038/s41586-018-0654-5 · DOI · Paper page
  14. Stephenson Jones, 2011, Evolutionary conservation of the basal ganglia as a common vertebrate mechanism for action selection, Curr Biol, 21, 1081, 10.1016/j.cub.2011.05.001 · DOI
  15. Ericsson, 2013, Evolutionarily conserved differences in pallial and thalamic short-term synaptic plasticity in striatum, J Physiol, 591, 859, 10.1113/jphysiol.2012.236869 · DOI
  16. Ericsson, 2013, Dopamine differentially modulates the excitability of striatal neurons of the direct and indirect pathways in lamprey, J Neurosci, 33, 8045, 10.1523/JNEUROSCI.5881-12.2013 · DOI
  17. Johansson, 2020, The functional organization of cortical and thalamic inputs onto five types of striatal neurons is determined by source and target cell identities, Cell Rep, 30, 1178, 10.1016/j.celrep.2019.12.095 · DOI
  18. Muñoz-Manchado, 2018, Diversity of interneurons in the dorsal striatum revealed by single-cell RNA sequencing and PatchSeq, Cell Rep, 24, 2179, 10.1016/j.celrep.2018.07.053 · DOI · Paper page
  19. Aristieta, 2021, A disynaptic circuit in the globus pallidus controls locomotion inhibition, Curr Biol, 31, 707, 10.1016/j.cub.2020.11.019 · DOI
  20. Ketzef, 2021, Differential synaptic input to external globus pallidus neuronal subpopulations in vivo, Neuron, 109, 516, 10.1016/j.neuron.2020.11.006 · DOI
  21. Mallet, 2012, Dichotomous organization of the external globus pallidus, Neuron, 74, 1075, 10.1016/j.neuron.2012.04.027 · DOI · Paper page
  22. Pérez-Fernández, 2017, Direct dopaminergic projections from the SNc modulate visuomotor transformation in the lamprey tectum, Neuron, 96, 910, 10.1016/j.neuron.2017.09.051 · DOI
  23. Pérez-Fernández, 2014, Evolutionarily conserved organization of the dopaminergic system in lamprey: SNc/VTA afferent and efferent connectivity and D2 receptor expression, J Comp Neurol, 522, 3775, 10.1002/cne.23639 · DOI
  24. Robertson, 2014, The lamprey blueprint of the mammalian nervous system, Prog Brain Res, 212, 337, 10.1016/B978-0-444-63488-7.00016-1 · DOI
  25. Thompson, 2008, Forebrain dopamine depletion impairs motor behavior in lamprey, Eur J Neurosci, 27, 1452, 10.1111/j.1460-9568.2008.06125.x · DOI
  26. da Silva, 2018, Dopamine neuron activity before action initiation gates and invigorates future movements, Nature, 554, 244, 10.1038/nature25457 · DOI
  27. Crittenden, 2016, Striosome-dendron bouquets highlight a unique striatonigral circuit targeting dopamine-containing neurons, Proc Natl Acad Sci U S A, 113, 11318, 10.1073/pnas.1613337113 · DOI
  28. Grillner, 2020, Basal ganglia-A motion perspective, Compr Physiol, 10, 1241, 10.1002/j.2040-4603.2020.tb00143.x · DOI
  29. Hikosaka, 2010, The habenula: from stress evasion to value-based decision-making, Nat Rev Neurosci, 11, 503, 10.1038/nrn2866 · DOI · Paper page
  30. Stephenson Jones, 2012, Evolutionary conservation of the habenular nuclei and their circuitry controlling the dopamine and 5-hydroxytryptophan (5-HT) systems, Proc Natl Acad Sci U S A, 109, E164, 10.1073/pnas.1119348109 · DOI
  31. Stephenson Jones, 2013, Independent circuits in the basal ganglia for the evaluation and selection of actions, Proc Natl Acad Sci U S A, 110, E3670, 10.1073/pnas.1314815110 · DOI
  32. Lazaridis, 2019, A hypothalamus-habenula circuit controls aversion, Mol Psychiatr, 24, 1351, 10.1038/s41380-019-0369-5 · DOI
  33. Stephenson Jones, 2016, A basal ganglia circuit for evaluating action outcomes, Nature, 539, 289, 10.1038/nature19845 · DOI
  34. Jung, 2018, The ancient origins of neural substrates for land walking, Cell, 172, 667, 10.1016/j.cell.2018.01.013 · DOI
  35. D'Elia, 2018, Development, functional organization, and evolution of vertebrate axial motor circuits, Neural Dev, 13, 10, 10.1186/s13064-018-0108-7 · DOI
  36. Grillner, 2020, Current principles of motor control, with special reference to vertebrate locomotion, Physiol Rev, 100, 271, 10.1152/physrev.00015.2019 · DOI · Paper page
  37. Song, 2016, Motor neurons control locomotor circuit function retrogradely via gap junctions, Nature, 529, 399, 10.1038/nature16497 · DOI
  38. Song, 2018, V2a interneuron diversity tailors spinal circuit organization to control the vigor of locomotor movements, Nat Commun, 9, 3370, 10.1038/s41467-018-05827-9 · DOI · Paper page
  39. Picton, 2021, A spinal organ of proprioception for integrated motor action feedback, Neuron, 109, 1188, 10.1016/j.neuron.2021.01.018 · DOI · Paper page
  40. Combes, 2004, Developmental segregation of spinal networks driving axial- and hindlimb-based locomotion in metamorphosing Xenopus laevis, J Physiol, 559, 17, 10.1113/jphysiol.2004.069542 · DOI
  41. Rauscent, 2006, Development and neuromodulation of spinal locomotor networks in the metamorphosing frog, J Physiol Paris, 100, 317, 10.1016/j.jphysparis.2007.05.009 · DOI
  42. Ha, 2018, Spinal Shox2 interneuron interconnectivity related to function and development, Elife, 7, 10.7554/eLife.42519 · DOI
  43. Gabitto, 2016, Bayesian sparse regression analysis documents the diversity of spinal inhibitory interneurons, Cell, 165, 220, 10.1016/j.cell.2016.01.026 · DOI · Paper page
  44. Sweeney, 2018, Origin and segmental diversity of spinal inhibitory interneurons, Neuron, 97, 341, 10.1016/j.neuron.2017.12.029 · DOI · Paper page
  45. Talpalar, 2013, Dual-mode operation of neuronal networks involved in left-right alternation, Nature, 500, 85, 10.1038/nature12286 · DOI
  46. Ruder, 2016, Long-distance descending spinal neurons ensure quadrupedal locomotor stability, Neuron, 92, 1063, 10.1016/j.neuron.2016.10.032 · DOI
  47. Ryczko, 2017, Nigral glutamatergic neurons control the speed of locomotion, J Neurosci, 37, 9759, 10.1523/JNEUROSCI.1810-17.2017 · DOI
  48. Caggiano, 2018, Midbrain circuits that set locomotor speed and gait selection, Nature, 553, 455, 10.1038/nature25448 · DOI
  49. Josset, 2018, Distinct contributions of mesencephalic locomotor region nuclei to locomotor control in the freely behaving mouse, Curr Biol, 28, 884, 10.1016/j.cub.2018.02.007 · DOI · Paper page
  50. Usseglio, 2020, Control of orienting movements and locomotion by projection-defined subsets of brainstem V2a neurons, Curr Biol, 30, 4665, 10.1016/j.cub.2020.09.014 · DOI · Paper page
  51. An, 2019, A cortical command circuit coordinates food handling and manipulation, Neuroscience, 2019
  52. Ruder, 2021, A functional map for diverse forelimb actions within brainstem circuitry, Nature, 590, 445, 10.1038/s41586-020-03080-z · DOI
  53. Ruder, 2019, Brainstem circuits controlling action diversification, Annu Rev Neurosci, 42, 485, 10.1146/annurev-neuro-070918-050201 · DOI · Paper page
  54. Lemon, 2019, Recent advances in our understanding of the primate corticospinal system, F1000Res, 8, 10.12688/f1000research.17445.1 · DOI
  55. Basso, 2021, Unraveling circuits of visual perception and cognition through the superior colliculus, Neuron, 109, 918, 10.1016/j.neuron.2021.01.013 · DOI
  56. Kardamakis, 2016, Spatiotemporal interplay between multisensory excitation and recruited inhibition in the lamprey optic tectum, Elife, 5, 10.7554/eLife.16472 · DOI
  57. Kardamakis, 2015, Tectal microcircuit generating visual selection commands on gaze-controlling neurons, Proc Natl Acad Sci U S A, 112, E1956, 10.1073/pnas.1504866112 · DOI
  58. Masullo, 2019, Genetically defined functional modules for spatial orienting in the mouse superior colliculus, Curr Biol, 29, 2892, 10.1016/j.cub.2019.07.083 · DOI
  59. Tokuoka, 2020, Anatomical and electrophysiological analysis of cholinergic inputs from the parabigeminal nucleus to the superficial superior colliculus, J Neurophysiol, 124, 1968, 10.1152/jn.00148.2020 · DOI
  60. Wilson, 2018, Three-dimensional representation of motor space in the mouse superior colliculus, Curr Biol, 28, 1744, 10.1016/j.cub.2018.04.021 · DOI
  61. Suzuki, 2019, The role of the optic tectum for visually evoked orienting and evasive movements, Proc Natl Acad Sci U S A, 116, 15272, 10.1073/pnas.1907962116 · DOI
  62. Förster, 2020, Retinotectal circuitry of larval zebrafish is adapted to detection and pursuit of prey, Elife, 9, 10.7554/eLife.58596 · DOI · Paper page

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Metadata

Authors
Grillner, S.
Venue
Current Opinion in Neurobiology
Publisher
Elsevier BV
Published
2021-12
Volume
71
Pages
11-18
ISSN
0959-4388
Cited by
47
References
12
Language
en

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