Comparative three-dimensional connectome map of motor cortical projections in the mouse brain

The motor cortex orchestrates simple to complex motor behaviors through its output projections to target areas. The primary (MOp) and secondary (MOs) motor cortices are known to produce specific output projections that are targeted to both similar and different target areas. These projections are further divided into layer 5 and 6 neuronal outputs, thereby producing four cortical outputs that may target other areas in a combinatorial manner. However, the precise network structure that integrates these four projections remains poorly understood. Here, we constructed a whole-brain, three-dimensional (3D) map showing the tract pathways and targeting locations of these four motor cortical outputs in mice. Remarkably, these motor cortical projections showed unique and separate tract pathways despite targeting similar areas. Within target areas, various combinations of these four projections were defined based on specific 3D spatial patterns, reflecting anterior-posterior, dorsal-ventral, and core-capsular relationships. This 3D topographic map ultimately provides evidence for the relevance of comparative connectomics: motor cortical projections known to be convergent are actually segregated in many target areas with unique targeting patterns, a finding that has anatomical value for revealing functional subdomains that have not been classified by conventional methods.

[1]  Allan R. Jones,et al.  A mesoscale connectome of the mouse brain , 2014, Nature.

[2]  Philippe Mailly,et al.  The Rat Prefrontostriatal System Analyzed in 3D: Evidence for Multiple Interacting Functional Units , 2013, The Journal of Neuroscience.

[3]  B. Sakmann,et al.  Whisker movements evoked by stimulation of single pyramidal cells in rat motor cortex , 2004, Nature.

[4]  Srinivas C. Turaga,et al.  Mapping social behavior-induced brain activation at cellular resolution in the mouse. , 2014, Cell reports.

[5]  J. Bourassa,et al.  Corticothalamic projections from the primary visual cortex in rats: a single fiber study using biocytin as an anterograde tracer , 1995, Neuroscience.

[6]  R. T. Watson,et al.  Efferent Connections of the Rostral Portion of Medial Agranular Cortex in Rats , 1987, Brain Research Bulletin.

[7]  Shinya Yamamoto,et al.  Thalamic afferent and efferent connectivity to cerebral cortical areas with direct projections to identified subgroups of trigeminal premotoneurons in the rat , 2010, Brain Research.

[8]  H C Kwan,et al.  Spatial organization of precentral cortex in awake primates. II. Motor outputs. , 1978, Journal of neurophysiology.

[9]  G. Fritsch,et al.  Electric excitability of the cerebrum (Über die elektrische Erregbarkeit des Grosshirns) , 2009, Epilepsy & Behavior.

[10]  E. Jones,et al.  Comprar The Thalamus 2 Volume Set | Edward G. Jones | 9780521858816 | Cambridge University Press , 2007 .

[11]  J. Poulet,et al.  Thalamic control of cortical states , 2012, Nature Neuroscience.

[12]  G. Shepherd,et al.  The neocortical circuit: themes and variations , 2015, Nature Neuroscience.

[13]  M. Deschenes,et al.  Corticothalamic projections from layer 5 of the vibrissal barrel cortex in the rat , 2000, The Journal of comparative neurology.

[14]  David R. Haynor,et al.  PET-CT image registration in the chest using free-form deformations , 2003, IEEE Transactions on Medical Imaging.

[15]  Y. Saalmann Intralaminar and medial thalamic influence on cortical synchrony, information transmission and cognition , 2014, Front. Syst. Neurosci..

[16]  John P Aggleton,et al.  Differential deficits in the Morris water maze following cytotoxic lesions of the anterior thalamus and fornix transection , 1998, Behavioural Brain Research.

[17]  E. Evarts,et al.  Relation of pyramidal tract activity to force exerted during voluntary movement. , 1968, Journal of neurophysiology.

[18]  P. Best,et al.  Mediodorsal thalamic lesions impair “Reference” and “working” memory in rats , 1990, Physiology & Behavior.

[19]  S. Wise,et al.  The motor cortex of the rat: Cytoarchitecture and microstimulation mapping , 1982, The Journal of comparative neurology.

[20]  T. Kita,et al.  The Subthalamic Nucleus Is One of Multiple Innervation Sites for Long-Range Corticofugal Axons: A Single-Axon Tracing Study in the Rat , 2012, The Journal of Neuroscience.

[21]  M. Deschenes,et al.  Axonal arborizations of corticostriatal and corticothalamic fibers arising from the second somatosensory area in the rat. , 1996, Cerebral cortex.

[22]  K. Kultas‐Ilinsky,et al.  Motor thalamic circuits in primates with emphasis on the area targeted in treatment of movement disorders , 2002, Movement disorders : official journal of the Movement Disorder Society.

[23]  I. Reichova,et al.  Somatosensory corticothalamic projections: distinguishing drivers from modulators. , 2004, Journal of neurophysiology.

[24]  Li I. Zhang,et al.  Linear Transformation of Thalamocortical input by Intracortical Excitation , 2013, Nature Neuroscience.

[25]  Naoki Yamawaki,et al.  Synaptic Circuit Organization of Motor Corticothalamic Neurons , 2015, The Journal of Neuroscience.

[26]  H. Seung,et al.  Serial two-photon tomography: an automated method for ex-vivo mouse brain imaging , 2011, Nature Methods.

[27]  Rebecca A Mease,et al.  Cortical control of adaptation and sensory relay mode in the thalamus , 2014, Proceedings of the National Academy of Sciences.

[28]  J. Kleim,et al.  The organization of the forelimb representation of the C57BL/6 mouse motor cortex as defined by intracortical microstimulation and cytoarchitecture. , 2011, Cerebral cortex.

[29]  Céline Cappe,et al.  The Thalamocortical Projection Systems in Primate: An Anatomical Support for Multisensory and Sensorimotor Interplay , 2009, Cerebral cortex.

[30]  Janita Turchi,et al.  Pulvinar Inactivation Disrupts Selection of Movement Plans , 2010, The Journal of Neuroscience.

[31]  H. Berthoud,et al.  The lateral hypothalamus as integrator of metabolic and environmental needs: From electrical self-stimulation to opto-genetics , 2011, Physiology & Behavior.

[32]  C. E. Elger,et al.  Cortico-spinal connections in the rat. I. Monosynaptic and polysynaptic responses of cervical motoneurons to epicortical stimulation , 1977, Experimental Brain Research.

[33]  Jun Tanji,et al.  Role for supplementary motor area cells in planning several movements ahead , 1994, Nature.

[34]  M. Deschenes,et al.  Intracortical Axonal Projections of Lamina VI Cells of the Primary Somatosensory Cortex in the Rat: A Single-Cell Labeling Study , 1997, The Journal of Neuroscience.

[35]  B. Balleine,et al.  Evidence of Action Sequence Chunking in Goal-Directed Instrumental Conditioning and Its Dependence on the Dorsomedial Prefrontal Cortex , 2009, The Journal of Neuroscience.

[36]  R. Lemon Descending pathways in motor control. , 2008, Annual review of neuroscience.

[37]  A. P. Georgopoulos,et al.  Neuronal population coding of movement direction. , 1986, Science.

[38]  M. Nicolelis,et al.  Sensorimotor encoding by synchronous neural ensemble activity at multiple levels of the somatosensory system. , 1995, Science.

[39]  S. Bressler,et al.  Large-scale brain networks in cognition: emerging methods and principles , 2010, Trends in Cognitive Sciences.

[40]  C. Gerfen,et al.  GENSAT BAC Cre-Recombinase Driver Lines to Study the Functional Organization of Cerebral Cortical and Basal Ganglia Circuits , 2013, Neuron.

[41]  Timothy H. Murphy,et al.  Distinct Cortical Circuit Mechanisms for Complex Forelimb Movement and Motor Map Topography , 2012, Neuron.

[42]  M. Graziano,et al.  Complex Movements Evoked by Microstimulation of Precentral Cortex , 2002, Neuron.

[43]  Daeyeol Lee,et al.  Role of rodent secondary motor cortex in value-based action selection , 2011, Nature Neuroscience.

[44]  J. Tanji,et al.  Relation of neurons in the nonprimary motor cortex to bilateral hand movement , 1987, Nature.

[45]  R. Turner,et al.  Corticostriatal Activity in Primary Motor Cortex of the Macaque , 2000, The Journal of Neuroscience.

[46]  Michael Brecht,et al.  Organization of rat vibrissa motor cortex and adjacent areas according to cytoarchitectonics, microstimulation, and intracellular stimulation of identified cells , 2004, The Journal of comparative neurology.

[47]  R. Guillery,et al.  On the actions that one nerve cell can have on another: distinguishing "drivers" from "modulators". , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[48]  S. Haber,et al.  The Organization of Prefrontal-Subthalamic Inputs in Primates Provides an Anatomical Substrate for Both Functional Specificity and Integration: Implications for Basal Ganglia Models and Deep Brain Stimulation , 2013, The Journal of Neuroscience.

[49]  Nikola T. Markov,et al.  A Weighted and Directed Interareal Connectivity Matrix for Macaque Cerebral Cortex , 2012, Cerebral cortex.

[50]  André Parent,et al.  Two different types of thalamic fibers innervate the rat striatum , 1995, Brain Research.

[51]  Tianyi Mao,et al.  A comprehensive thalamocortical projection map at the mesoscopic level , 2014, Nature Neuroscience.

[52]  K. Khodakhah,et al.  Short latency cerebellar modulation of the basal ganglia , 2014, Nature Neuroscience.

[53]  M. Deschenes,et al.  Corticothalamic projections from layer V cells in rat are collaterals of long-range corticofugal axons , 1994, Brain Research.

[54]  Kevin D Alloway,et al.  Contralateral corticothalamic projections from MI whisker cortex: Potential route for modulating hemispheric interactions , 2008, The Journal of comparative neurology.

[55]  Thomas J. Davidson,et al.  Closed-loop optogenetic control of thalamus as a new tool to interrupt seizures after cortical injury , 2012, Nature Neuroscience.

[56]  Kevin D Alloway,et al.  Bilateral projections from rat MI whisker cortex to the neostriatum, thalamus, and claustrum: Forebrain circuits for modulating whisking behavior , 2009, The Journal of comparative neurology.

[57]  Anna S. Mitchell,et al.  Dissociable memory effects after medial thalamus lesions in the rat , 2005, The European journal of neuroscience.

[58]  Rui M. Costa,et al.  Motor Learning Consolidates Arc-Expressing Neuronal Ensembles in Secondary Motor Cortex , 2015, Neuron.

[59]  B. Alstermark,et al.  Lack of monosynaptic corticomotoneuronal EPSPs in rats: disynaptic EPSPs mediated via reticulospinal neurons and polysynaptic EPSPs via segmental interneurons. , 2004, Journal of neurophysiology.

[60]  Grigori N. Orlovsky,et al.  Activity of Different Classes of Neurons of the Motor Cortex during Postural Corrections , 2003, The Journal of Neuroscience.

[61]  Zengcai V. Guo,et al.  A motor cortex circuit for motor planning and movement , 2015, Nature.

[62]  Paul Cisek,et al.  Neural activity in primary motor and dorsal premotor cortex in reaching tasks with the contralateral versus ipsilateral arm. , 2003, Journal of neurophysiology.

[63]  P. Salin,et al.  Deep Brain Stimulation of the Center Median–Parafascicular Complex of the Thalamus Has Efficient Anti-Parkinsonian Action Associated with Widespread Cellular Responses in the Basal Ganglia Network in a Rat Model of Parkinson's Disease , 2010, The Journal of Neuroscience.

[64]  Charles R. Gerfen,et al.  Targeting Cre Recombinase to Specific Neuron Populations with Bacterial Artificial Chromosome Constructs , 2007, The Journal of Neuroscience.

[65]  Arthur W. Toga,et al.  Neural Networks of the Mouse Neocortex , 2014, Cell.

[66]  R. Guillery,et al.  The thalamus as a monitor of motor outputs. , 2002, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[67]  Mario Wiesendanger,et al.  Patterns of corticothalamic terminations following injection of Phaseolus vulgaris leucoagglutinin (PHA-L) in the sensorimotor cortex of the rat , 1991, Neuroscience Letters.

[68]  E. Rouiller,et al.  Comparison of the connectional properties of the two forelimb areas of the rat sensorimotor cortex: support for the presence of a premotor or supplementary motor cortical area. , 1993, Somatosensory & motor research.

[69]  Zachary F Mainen,et al.  Neural antecedents of self-initiated actions in secondary motor cortex , 2014, Nature Neuroscience.