Cerebellothalamic and thalamostriatal projections in a songbird, the Bengalese Finch Pubblico
Nicholson, David (Fall 2017)
Abstract
Like a child learning to speak, songbirds learn their songs as juveniles from adult tutors. They then perfect their song by practicing it thousands of times during development. This behavior makes songbirds an excellent model system through which neuroscientists can understand how the brain learns and produces a motor skill that resembles speech. Birdsong is under the control of a network of nuclei in the songbird brain known as the song system. To what extent is the song system like motor systems in the mammalian brain? Many studies have shown how a thalamocortical-basal ganglia loop in the song system known as the Anterior Forebrain Pathway (AFP) contributes to learning song and adaptively maintaining it in adulthood. In mammals, the basal ganglia receive input from the thalamus, including thalamic regions that receive output from the cerebellum. It is unknown whether the basal ganglia nucleus of the song system, Area X, receives thalamic input, or whether such inputs might be used to convey cerebellar outputs to the song system. I first demonstrate that the cerebellum projects to dorsal thalamus in the Bengalese finch, and provide the first detailed description of the cerebellothalamic projections. Then, using a viral vector that specifically labels presynaptic axon terminals, I demonstrate that dorsal thalamus projects to the striatum. To determine the sources and targets of the thalamostriatal system in songbirds, I use tracers to map thalamic regions and immunohistochemistry to identify song system nuclei. I find that DLM and immediately adjacent DTCbN project to Area X. In contrast, more medial and ventral subregions of DTCbN project to striatum outside Area X. These results suggest that in the AFP the basal ganglia integrates feedback from the thalamic region to which it projects as well as input from thalamic regions that receive cerebellar output, much like the mammalian basal ganglia.
Table of Contents
List of Figures and Tables xiv
List of Abbreviations xvii
I Introduction 1
I.1 Songbirds as a model system 2
I.1.A Parallels between birdsong, speech, and similar motor skills 2
I.1.A.1 Sensorimotor learning 3
I.1.A.2 Social interaction 5
I.2 The song system as a general model of motor systems 6
I.2.A.1 The motor system in mammals 8
I.2.A.2 The song system in songbirds 11
I.2.A.3 The basal ganglia in mammals and songbirds 13
I.2.A.3.a Mammalian basal ganglia anatomy 14
I.2.A.3.b Songbird basal ganglia anatomy 15
I.2.A.3.c Basal ganglia output to motor thalamus 20
I.2.A.3.d Basal ganglia output to thalamus in the AFP 23
I.2.A.3.e Basal ganglia function and theoretical models 25
I.2.A.3.f Reinforcement learning in the AFP 32
I.2.A.4 The thalamostriatal system: anatomy, physiology, and theories about computation 34
I.2.A.4.a.1 Anatomy: two types of thalamostriatal projection neurons 34
I.2.A.4.a.2 Anatomy: afferents of the intralaminar nuclei 39
I.2.A.4.a.3 Physiology and function of the thalamostriatal system 41
I.2.A.5 Cerebellum: anatomy, physiology, and theories about computation 43
I.2.A.5.a.1 Cerebellothalamic system: anatomy 46
I.2.A.5.a.2 Cerebellothalamic system: physiology and proposed function 54
I.2.A.5.a.3 Other relevant cerebellar pathways 59
I.2.A.5.a.4 Cerebellar function in speech 61
I.2.A.5.b Possible interactions between the basal ganglia and cerebellum 63
I.2.A.5.c Motor control of speech 64
I.2.B Open question about the song system: does the song system contain a thalamostriatal projection? 68
I.2.B.1.a Evidence for a thalamostriatal system in birds 69
I.2.C Open question about the song system: is there a route through thalamus from the cerebellar nuclei to the song system? 76
I.2.D Non-classical components of the song system 77
I.2.D.1 Descending motor pathways in the avian brain 77
I.2.D.2 Other connections 82
I.2.D.3 Hypothesized evolutionary origins of neural pathways for vocal behavior 83
I.3 Overview of studies in this dissertation 84
II Methods 86
II.1 Surgery and tissue collection. 86
II.2 Immunohistochemistry 88
II.3 Production and specificity of antisera 89
II.4 Microscopy, digital photography, and image processing. 92
II.5 “Drawings” of signal from lentiviral injections. 93
II.6 Map of dorsal thalamus 94
III Results 96
III.1 The cerebellar nuclei in Bengalese Finches project to dorsal thalamus 96
III.1.A CbL projects to dorsal thalamus 96
III.1.B CbI and CbM also project to dorsal thalamus 100
III.2 Dorsal thalamus in Bengalese Finches projects to Area X 103
III.2.A DLM and the immediately adjacent DTCbN project to Area X 105
III.2.B More medial and ventral DTCbN projects to medial striatum outside of Area X 107
IV Discussion 109
IV.1 Technical considerations, and relation to previous work 110
IV.1.A Cerebellothalamic projections 110
IV.1.B Thalamostriatal projections 112
IV.1.C Disynaptic pathway from CbN to Area X through DTCbN 115
IV.2 Functional implications and future studies 117
IV.2.A Thalamostriatal projections 117
IV.2.A.1 Microcircuitry of Area X, including thalamostriatal projections: ultrastructural studies 117
IV.2.A.2 Topography and morphology of thalamostriatal projections: single-cell reconstruction studies 119
IV.2.A.3 Cell types in Area X targeted by thalamostriatal projections: immunohistochemical studies 122
IV.2.A.4 Subcortical inputs to dorsal thalamus: retrograde tracer and immunohistochemical studies 125
IV.2.A.5 Efferents of dorsal thalamic subregions: studies with iontophoretic injections of AAV 126
IV.2.A.6 Physiology of thalamostriatal projections 127
IV.2.A.7 Determine nature of information relayed to DLM and DTCbN by subcortical inputs 131
IV.2.B Cerebellothalamic projections 132
IV.2.B.1 Is the projection from CbN to thalamus glutamatergic? Can immunostain for glutamatergic and GABAergic inputs to dorsal thalamus serve as a proxy for pallidal and cerebellar inputs? A combined tracer and immunohistochemical study. 133
IV.2.B.2 Disynaptic pathways from CbN to the forebrain through thalamus: a study with transsynaptic tracers 134
IV.2.B.3 Specificity of projections of the cerebellar nuclei: tracer studies 135
IV.2.B.4 Does the cerebellum interact with VTA? 137
IV.2.B.5 Disynaptic pathways from CbN to the forebrain through thalamus: physiological studies 139
IV.2.B.6 Does the cerebellum or red nucleus interact with phonatory or respiratory nuclei in the brainstem? Tracer studies 140
IV.2.B.7 Cerebellar involvement with beak movements: behavioral and physiological studies 141
IV.2.B.8 Is the cerebellum involved in sensorimotor learning or in social interaction? 145
IV.2.B.9 Does the cerebellum co-ordinate dancing during song? 147
IV.2.C Functional considerations and conclusions 149
IV.2.C.1 Cerebellothalamic system 149
IV.2.C.2 Thalamostriatal projections 150
V Appendices 152
V.1 Introduction 152
V.2 Afferents and efferents of the Bengalese finch cerebellar nuclei 152
V.2.A Comparison of projections of CbL and CbI to dorsal thalamus 152
V.2.B SpM sends collaterals to dorsal thalamus 154
V.2.C CbL projects to several other regions in the midbrain 156
V.2.D Input from cerebellar folia to CbL 160
V.3 Regions of dorsal thalamus in Bengalese finches 161
V.3.A DLM as defined by projections from Area X 161
V.3.B DIP as defined by projections from globus pallidus 163
V.4 Relation of CbL projections to other song system nuclei in dorsal thalamus 165
V.4.A CbL axon terminals in some cases closely appose thalamic neurons retrogradely labeled by injections in Area X 165
V.4.B CbL does not project to thalamic song system nucleus DMP 167
V.4.C CbL does not project to thalamic song system nucleus Uva 169
V.4.D CbN axon terminals closely appose dendrites and soma of neurons in dorsal thalamus that project to nidopallium 171
V.4.E Lentiviral vector injections in DIVA labeled HA 173
V.4.F Discussion of additional anatomical results 174
V.5 Possible cerebellar contributions to song 176
V.5.A Electrolytic lesions of CbL do not produce gross distortions of song 176
V.5.B Electrolytic lesions of CbL can have long term effects on acoustic parameters 178
V.5.C Electrolytic lesions of CbL do not impair the ability to change song in response to aversive reinforcement experiments 179
V.5.D Discussion of results from electrolytic lesions of CbL 179
V.6 Additional methods 181
V.6.A Additional stereotactic co-ordinates and tracer injection methods 181
V.6.B Electroylytic lesions of CbL 182
V.6.C Histology and estimate of size of CbL lesions 182
V.6.D Measurement of effect of CbL lesions on acoustic parameters 183
V.6.E Aversive reinforcement experiments 184
VI References 187
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