Clarke's column neurons as the focus of a corticospinal corollary circuit

Nature Neuroscience

Volumn 13, Issue 10, 2010, Pages 1233-1239

  Hantman, Adam W ^a   Jessell, Thomas M ^a  

^a Columbia University ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANATOMICAL CONCEPTS; ANIMAL EXPERIMENT; ARTICLE; CLARKE COLUMN; CONTROLLED STUDY; EXCITATORY POSTSYNAPTIC POTENTIAL; INHIBITORY POSTSYNAPTIC POTENTIAL; LUMBAR SPINE; MOUSE; NERVE CELL; NEUROANATOMY; NEUROPHYSIOLOGY; NONHUMAN; PRIORITY JOURNAL; PROPRIOCEPTION; PYRAMIDAL TRACT; SENSORY NERVE CELL; SPINE; SPINOCEREBELLAR TRACT; THORACIC SPINE; ANALOGS AND DERIVATIVES; ANIMAL; BIOLOGICAL MODEL; CEREBELLUM; CYTOLOGY; DRUG EFFECTS; ELECTROSTIMULATION; GENE EXPRESSION REGULATION; GENETICS; MEMBRANE POTENTIAL; METABOLISM; NERVE CELL INHIBITION; NERVE CELL NETWORK; NERVE TRACT; NEWBORN; PATCH CLAMP TECHNIQUE; PHYSIOLOGY; PROCEDURES; SENSORY FEEDBACK; SPINAL CORD; TRANSGENIC MOUSE;

6-CYANO-7-NITROQUINOXALINE-2,3-DIONE; ANIMALS; ANIMALS, NEWBORN; BETA-GALACTOSIDASE; BICUCULLINE; CEREBELLUM; CHOLERA TOXIN; ELECTRIC STIMULATION; ESTROGEN ANTAGONISTS; EXCITATORY AMINO ACID ANTAGONISTS; FEEDBACK, SENSORY; GABA ANTAGONISTS; GENE EXPRESSION REGULATION; GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR; GLYCINE AGENTS; GLYCINE PLASMA MEMBRANE TRANSPORT PROTEINS; GREEN FLUORESCENT PROTEINS; HOMEODOMAIN PROTEINS; LYSINE; MEMBRANE POTENTIALS; MICE; MICE, TRANSGENIC; MODELS, NEUROLOGICAL; NERVE NET; NEURAL INHIBITION; NEURAL PATHWAYS; PARVALBUMINS; PATCH-CLAMP TECHNIQUES; PROTEIN KINASE C; RNA, MESSENGER; SENSORY RECEPTOR CELLS; SPINAL CORD; STILBAMIDINES; STRYCHNINE; TAMOXIFEN; TAU PROTEINS; TRANSCRIPTION FACTORS; VESICULAR GLUTAMATE TRANSPORT PROTEIN 1;

2-HYDROXY-4,4'-DIAMIDINOSTILBENE, METHANESULFONATE SALT; 4 AMINOBUTYRIC ACID RECEPTOR BLOCKING AGENT; 6 CYANO 7 NITRO 2,3 QUINOXALINEDIONE; AMINO ACID RECEPTOR AFFECTING AGENT; AMINO ACID RECEPTOR BLOCKING AGENT; ANTIESTROGEN; BETA GALACTOSIDASE; BICUCULLINE; BIOCYTIN; CHOLERA TOXIN; EMPTY SPIRACLES HOMEOBOX PROTEINS; GLIAL CELL LINE DERIVED NEUROTROPHIC FACTOR; GLYCINE TRANSPORTER; GREEN FLUORESCENT PROTEIN; HOMEODOMAIN PROTEIN; LYSINE; MESSENGER RNA; PARVALBUMIN; PROTEIN KINASE C; SLC17A7 PROTEIN, MOUSE; SLC6A5 PROTEIN, MOUSE; STILBAMIDINE; STRYCHNINE; TAMOXIFEN; TAU PROTEIN; TRANSCRIPTION FACTOR; VESICULAR GLUTAMATE TRANSPORTER 1;

EID: 77957260955     PISSN: 10976256     EISSN: None     Source Type: Journal    
DOI: 10.1038/nn.2637     Document Type: Article

References (41)

1. Eccles, J.C., Oscarsson, O. & Willis, W.D. Synaptic action of group I and II afferent fbres of muscle on the cells of the dorsal spinocerebellar tract. J. Physiol. (Lond.) 158, 517-543 (1961).
2. Lundberg, A. Ascending spinal hindlimb pathways in the cat. Prog. Brain Res. 12, 135-163 (1964).
3. Oscarsson, O. Functional organization of the spino-and cuneocerebellar tracts. Physiol. Rev. 45, 495-522 (1965).
4. Bosco, G. & Poppele, R.E. Proprioception from a spinocerebellar perspective. Physiol. Rev. 81, 539-568 (2001).
5. Matsushita, M. & Hosoya, Y. Cells of origin of the spinocerebellar tract in the rat, studied with the method of retrograde transport of horseradish peroxidase. Brain Res. 173, 185-200 (1979).
6. Edgley, S.A. & Jankowska, E. Information processed by dorsal horn spinocerebellar tract neurones in the cat. J. Physiol. (Lond.) 397, 81-97 (1988).
7. Walmsley, B. Central synaptic transmission: studies at the connection between primary afferent fbres and dorsal spinocerebellar tract (DSCT) neurones in Clarke's column of the spinal cord. Prog. Neurobiol. 36, 391-423 (1991).
8. Hongo, T. et al. Trajectory of group Ia and Ib fbers from the hind-limb muscles at the L3 and L4 segments of the spinal cord of the cat. J. Comp. Neurol. 262, 159-194 (1987).
9. Mann, M.D. Clarke's column and the dorsal spinocerebellar tract: a review. Brain Behav. Evol. 7, 34-83 (1973).
10. Wolpert, D.M., Ghahramani, Z. & Jordan, M.I. An internal model for sensorimotor integration. Science 269, 1880-1882 (1995).
11. Wolpert, D.M. & Miall, R.C. Forward models for physiological motor control. Neural Netw. 9, 1265-1279 (1996).
12. Sommer, M.A. & Wurtz, R.H. A pathway in primate brain for internal monitoring of movements. Science 296, 1480-1482 (2002)
13. Jeannerod, M. Motor Cognition: What Actions Tell the Self 1-21 (Oxford University Press, Oxford, 2006).
14. Roy, J.E. & Cullen, K.E. Selective processing of vestibular reafference during self-generated head motion. J. Neurosci. 21, 2131-2142 (2001).
15. Mulliken, G.H., Musallam, S. & Andersen, R.A. Forward estimation of movement state in posterior parietal cortex. Proc. Natl. Acad. Sci. USA 105, 8170-8177 (2008).
16. Ebner, T.J. & Pasalar, S. Cerebellum predicts the future motor state. Cerebellum 7, 583-588 (2008).
17. Seki, K., Perlmutter, S.I. & Fetz, E.E. Sensory input to primate spinal cord is presynaptically inhibited during voluntary movement. Nat. Neurosci. 6, 1309-1316 (2003).
18. Hongo, T. & Okada, Y. Cortically evoked pre-and postsynaptic inhibition of impulse transmission to the dorsal spinocerebellar tract. Exp. Brain Res. 3, 163-177 (1967).
19. Hongo, T., Okada, Y. & Sato, M. Corticofugal infuences on transmission to the dorsal spinocerebellar tract from hindlimb primary afferents. Exp. Brain Res. 3, 135-149 (1967).
20. Mott, F. Microscopical examination of Clarke's column in man, the monkey and the dog. J. Anat. Physiol. 22, 479-495 (1888).
21. Nosrat, C.A. et al. Cellular expression of GDNF mRNA suggests multiple functions inside and outside the nervous system. Cell Tissue Res. 286, 191-207 (1996).
22. Moore, M.W. et al. Renal and neuronal abnormalities in mice lacking GDNF. Nature 382, 76-79 (1996).
23. Hippenmeyer, S. et al. A developmental switch in the response of DRG neurons to ETS transcription factor signaling. PLoS Biol. 3, e159 (2005).
24. Matsushita, M. & Gao, X. Projections from the thoracic cord to the cerebellar nuclei in the rat, studied by anterograde axonal tracing. J. Comp. Neurol. 386, 409-421 (1997).
25. Dumitriu, D., Cossart, R., Huang, J. & Yuste, R. Correlation between axonal morphologies and synaptic input kinetics of interneurons from mouse visual cortex. Cereb. Cortex 17, 81-91 (2007).
26. Yoshida, Y., Han, B., Mendelsohn, M. & Jessell, T.M. PlexinA1 signaling directs the segregation of proprioceptive sensory axons in the developing spinal cord. Neuron 52, 775-788 (2006).
27. Alvarez, F.J., Villalba, R.M., Zerda, R. & Schneider, S.P. Vesicular glutamate transporters in the spinal cord, with special reference to sensory primary afferent synapses. J. Comp. Neurol. 472, 257-280 (2004).
28. Bareyre, F.M., Kerschensteiner, M., Misgeld, T. & Sanes, J.R. Transgenic labeling of the corticospinal tract for monitoring axonal responses to spinal cord injury. Nat. Med. 11, 1355-1360 (2005).
29. Finger, J.H. et al. The netrin 1 receptors Unc5h3 and Dcc are necessary at multiple choice points for the guidance of corticospinal tract axons. J. Neurosci. 22, 10346-10356 (2002).
30. López-Bendito, G. et al. Preferential origin and layer destination of GAD65-GFP cortical interneurons. Cereb. Cortex 14, 1122-1133 (2004).
31. Lomelí, J., Quevedo, J., Linares, P. & Rudomin, P. Local control of information fow in segmental and ascending collaterals of single afferents. Nature 395, 600-604 (1998).
32. Betley, J.N. et al. Stringent specifcity in the construction of a GABAergic presynaptic inhibitory circuit. Cell 139, 161-174 (2009).
33. Prochazka, A., Gillard, D. & Bennett, D.J. Implications of positive feedback in the control of movement. J. Neurophysiol. 77, 3237-3251 (1997).
34. Arshavsky, Y.I., Berkinblit, M.B., Fukson, O.I., Gelfand, I.M. & Orlovsky, G.N. Origin of modulation in neurones of the ventral spinocerebellar tract during locomotion. Brain Res. 43, 276-279 (1972).
35. Arshavsky, Y.I., Gelfand, I.M., Orlovsky, G.N., Pavlova, G.A. & Popova, L.B. Origin of signals conveyed by the ventral spino-cerebellar tract and spino-reticulo-cerebellar pathway. Exp. Brain Res. 54, 426-431 (1984).
36. Lundberg, A. Function of the ventral spinocerebellar tract. A new hypothesis. Exp. Brain Res. 12, 317-330 (1971).
37. Poulet, J.F. & Hedwig, B. The cellular basis of a corollary discharge. Science 311, 518-522 (2006).
38. Blakemore, S.J. & Sirigu, A. Action prediction in the cerebellum and in the parietal lobe. Exp. Brain Res. 153, 239-245 (2003).
39. Gorski, J.A. et al. Cortical excitatory neurons and glia, but not GABAergic neurons, are produced in the Emx1-expressing lineage. J. Neurosci. 22, 6309-6314 (2002).
40. Arsénio Nunes, M.L. & Sotelo, C. Development of the spinocerebellar system in the postnatal rat. J. Comp. Neurol. 237, 291-306 (1985).
41. Hantman, A.W., van den Pol, A.N. & Perl, E.R. Morphological and physiological features of a set of spinal substantia gelatinosa neurons defned by green fuorescent protein expression. J. Neurosci. 24, 836-842 (2004).