Thalamic inputs to striatal interneurons in monkeys: synaptic organization and co-localization of calcium binding proteins

Recent studies indicate that extrinsic inputs from sensorimotor regions of the cerebral cortex and the centromedian intralaminar thalamic nucleus terminate preferentially upon specific subpopulations of striatal output neurons in monkeys. The objective of the present study was to verify whether this specificity of innervation also characterizes the synaptic interactions between thalamic inputs from the centromedian nucleus and the four major populations of striatal interneurons. This was achieved by double labelling techniques at the electron microscope level, combining the anterograde transport of biotinylated-dextran amine with the immunostaining for specific markers of striatal interneurons (somatostatin, parvalbumin, choline acetyltransferase and calretinin). Injections of biotinylated-dextran amine in the centromedian nucleus led to dense bands of anterograde labelling which, in double immunostained sections, largely overlapped with the four populations of interneurons in the post-commissural region of the putamen. In the electron microscope, biotinylated-dextran amine-containing terminals formed asymmetric axo-dendritic synapses with somatostatin-, parvalbumin-, and choline acetyltransferase-containing elements. However, synapses between anterogradely labelled terminals and calretinin-positive neurons were not found. In sections processed to localize biotinylated-dextran amine and parvalbumin or calretinin, double-labelled terminals (biotinylated-dextran amine/parvalbumin and biotinylated-dextran amine/calretinin), morphologically similar to thalamostriatal boutons, were found in the striatum indicating that calcium binding proteins may be expressed by thalamostriatal neurons. To test this possibility, we combined the retrograde transport of lectin-conjugated horseradish peroxidase from the putamen with parvalbumin and calretinin immunostaining and found that, indeed, most of the retrogradely labelled cells in the centromedian nucleus displayed parvalbumin and calretinin immunoreactivity. Moreover, co-localization studies revealed that calretinin and parvalbumin co-exist in single neurons of the centromedian nucleus. In conclusion, striatal interneurons immunoreactive for somatostatin, parvalbumin and choline acetyltransferase, but not those containing calretinin, receive strong inputs from the centromedian nucleus in monkeys. Moreover, our findings indicate that parvalbumin and calretinin co-exist in individual thalamostriatal neurons. In combination with our previous data, these results suggest that thalamic information may be conveyed to striatal projection neurons both, directly via excitatory synaptic inputs, or indirectly via striatal interneurons. The relative importance of those direct and indirect thalamic influences upon the activity of striatal output neurons remains to be established.

[1]  Solomon H. Snyder,et al.  Nitric oxide, a novel neuronal messenger , 1992, Neuron.

[2]  E. G. Jones,et al.  Differential Calcium Binding Protein Immunoreactivity Distinguishes Classes of Relay Neurons in Monkey Thalamic Nuclei , 1989, The European journal of neuroscience.

[3]  B. D. Bennett,et al.  Characterization of calretinin-immunoreactive structures in the striatum of the rat , 1993, Brain Research.

[4]  B. D. Bennett,et al.  Synaptic input and output of parvalbumin-immunoreactive neurons in the neostriatum of the rat , 1994, Neuroscience.

[5]  A. Parent,et al.  Synaptic relationships between dopaminergic afferents and cortical or thalamic input in the sensorimotor territory of the striatum in monkey , 1994, The Journal of comparative neurology.

[6]  S. Consolo,et al.  Trans‐synaptic Modulation of Striatal ACh Release In Vivo by the Parafascicular Thalamic Nucleus , 1995, The European journal of neuroscience.

[7]  D. James Surmeier,et al.  Muscarinic modulation of a transient K+ conductance in rat neostriatal neurons , 1990, Nature.

[8]  N. Aronin,et al.  Ultrastructural features of immunoreactive somatostatin neurons in the rat caudate nucleus , 1982, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  D. Jacobowitz,et al.  Calretinin distribution in the thalamus of the rat: Immunohistochemical and in situ hybridization histochemical analyses , 1992, Neuroscience.

[10]  B. Wainer,et al.  Stabilization of the tetramethylbenzidine (TMB) reaction product: application for retrograde and anterograde tracing, and combination with immunohistochemistry. , 1984, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[11]  F. Wouterlood,et al.  Double-label immunocytochemistry: combination of anterograde neuroanatomical tracing with Phaseolus vulgaris leucoagglutinin and enzyme immunocytochemistry of target neurons. , 1987, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[12]  Y. Kawaguchi,et al.  Large aspiny cells in the matrix of the rat neostriatum in vitro: physiological identification, relation to the compartments and excitatory postsynaptic currents. , 1992, Journal of neurophysiology.

[13]  O. Bosler,et al.  Striatal NPY‐Containing Neurons Receive GABAergic Afferents and may also Contain GABA: An Electron Microscopic Study in the Rat , 1990, European Journal of Neuroscience.

[14]  A. Parent,et al.  Calretinin-immunoreactive neurons in the human striatum , 1995, Brain Research.

[15]  A. Parent,et al.  Neuropeptide Y-immunoreactive neurons in the striatum of cat and monkey: Morphological characteristics, intrinsic organization and co-localization with somatostatin , 1986, Brain Research.

[16]  P Buchwald,et al.  Characterization of a polyclonal antiserum against the purified human recombinant calcium binding protein calretinin. , 1993, Cell calcium.

[17]  Charles J. Wilson,et al.  Parvalbumin‐containing gabaergic interneurons in the rat neostriatum , 1990, The Journal of comparative neurology.

[18]  A. Parent,et al.  Cortical input to parvalbumin-immunoreactive neurones in the putamen of the squirrel monkey , 1992, Brain Research.

[19]  Françoise Condé,et al.  Local circuit neurons immunoreactive for calretinin, calbindin D‐28k or parvalbumin in monkey prefronatal cortex: Distribution and morphology , 1994, The Journal of comparative neurology.

[20]  C. Gerfen The neostriatal mosaic: multiple levels of compartmental organization in the basal ganglia. , 1992, Annual review of neuroscience.

[21]  K. Baimbridge,et al.  Calcium-binding proteins in the nervous system , 1992, Trends in Neurosciences.

[22]  J. Rogers,et al.  Calretinin and calbindin-D28k in rat brain: Patterns of partial co-localization , 1992, Neuroscience.

[23]  A M Graybiel,et al.  Cortically Driven Immediate-Early Gene Expression Reflects Modular Influence of Sensorimotor Cortex on Identified Striatal Neurons in the Squirrel Monkey , 1997, The Journal of Neuroscience.

[24]  J. Bolam,et al.  Cholinergic synaptic input to different parts of spiny striatonigral neurons in the rat , 1988, The Journal of comparative neurology.

[25]  Y. Smith,et al.  Differential synaptic innervation of striatofugal neurones projecting to the internal or external segments of the globus pallidus by thalamic afferents in the squirrel monkey , 1996, The Journal of comparative neurology.

[26]  P. Somogyi,et al.  Monosynaptic cortical input and local axon collaterals of identified striatonigral neurons. A light and electron microscopic study using the golgi‐peroxidase transport‐degeneration procedure , 1981, The Journal of comparative neurology.

[27]  S. Hsu,et al.  Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. , 1981, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[28]  A. Reiner,et al.  Biotinylated dextran amine as an anterograde tracer for single- and double-labeling studies , 1992, Journal of Neuroscience Methods.

[29]  M M Mesulam,et al.  A light and electron microscopic procedure for sequential double antigen localization using diaminobenzidine and benzidine dihydrochloride. , 1986, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[30]  I. Llewellyn-Smith,et al.  The tungstate-stabilized tetramethylbenzidine reaction for light and electron microscopic immunocytochemistry and for revealing biocytin-filled neurons , 1993, Journal of Neuroscience Methods.

[31]  A. Graybiel,et al.  Temporal and spatial characteristics of tonically active neurons of the primate's striatum. , 1995, Journal of neurophysiology.

[32]  A. Parent,et al.  Complementary Distribution of Calbindin D‐28k and Parvalbumin in the Basal Forebrain and Midbrain of the Squirrel Monkey , 1991, The European journal of neuroscience.

[33]  Y. Kawaguchi Neostriatal cell subtypes and their functional roles , 1997, Neuroscience Research.

[34]  S. T. Kitai,et al.  Firing patterns and synaptic potentials of identified giant aspiny interneurons in the rat neostriatum , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[35]  T. Pasik,et al.  Ultrastructure of Golgi-impregnated and gold-toned spiny and aspiny neurons in the monkey neostriatum , 1980, Journal of neurocytology.

[36]  T. Powell,et al.  The termination of fibres from the cerebral cortex and thalamus upon dendritic spines in the caudate nucleus: a study with the Golgi method. , 1971, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[37]  J. Carey,et al.  Large neurons in the primate neostriatum examined with the combined Golgi‐electron microscopic method , 1986, The Journal of comparative neurology.

[38]  H. Groenewegen,et al.  The specificity of the ‘nonspecific’ midline and intralaminar thalamic nuclei , 1994, Trends in Neurosciences.

[39]  G. Leuba,et al.  Colocalization of parvalbumin, calretinin and calbindin D-28k in human cortical and subcortical visual structures , 1997, Journal of Chemical Neuroanatomy.

[40]  A. Parent,et al.  Differential connections of caudate nucleus and putamen in the squirrel monkey (Saimiri sciureus) , 1986, Neuroscience.

[41]  Charles J. Wilson,et al.  Fine structure and synaptic connections of the common spiny neuron of the rat neostriatum: A study employing intracellular injection of horseradish peroxidase , 1980 .

[42]  F. Olucha,et al.  A new stabilizing agent for the tetramethyl benzidine (TMB) reaction product in the histochemical detection of horseradish peroxidase (HRP) , 1985, Journal of Neuroscience Methods.

[43]  T. Pasik,et al.  A Golgi study of neuronal types in the neostriatum of monkeys , 1976, Brain Research.

[44]  M. Celio,et al.  Calbindin D-28k and parvalbumin in the rat nervous system , 1990, Neuroscience.

[45]  A. Parent Extrinsic connections of the basal ganglia , 1990, Trends in Neurosciences.

[46]  B. D. Bennett,et al.  Localisation of parvalbumin‐immunoreactive structures in primate caudate‐putamen , 1994, The Journal of comparative neurology.

[47]  Y. Kawaguchi,et al.  Physiological, morphological, and histochemical characterization of three classes of interneurons in rat neostriatum , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[48]  I. Grofová The identification of striatal and pallidal neurons projecting to substantia nigra An experimental study by means of retrograde axonal transport of horseradish peroxidase , 1975, Brain Research.

[49]  B. Gulyás,et al.  Activation by Attention of the Human Reticular Formation and Thalamic Intralaminar Nuclei , 1996, Science.

[50]  H. Kita,et al.  Parvalbumin-immunoreactive neurons in the rat neostriatum: a light and electron microscopic study , 1990, Brain Research.

[51]  A. Parent,et al.  Efferent connections of the centromedian and parafascicular thalamic nuclei in the squirrel monkey: A light and electron microscopic study of the thalamostriatal projection in relation to striatal heterogeneity , 1992, The Journal of comparative neurology.

[52]  J. DeFelipe,et al.  Neocortical neuronal diversity: chemical heterogeneity revealed by colocalization studies of classic neurotransmitters, neuropeptides, calcium-binding proteins, and cell surface molecules. , 1993, Cerebral cortex.

[53]  B. D. Bennett,et al.  Localisation of Calcium Binding Proteins in the Neostriatum , 1994 .

[54]  C. Gerfen,et al.  D1 and D2 dopamine receptor-regulated gene expression of striatonigral and striatopallidal neurons. , 1990, Science.

[55]  A. D. Smith,et al.  Identification of synaptic terminals of thalamic or cortical origin in contact with distinct medium‐size spiny neurons in the rat neostriatum , 1988, The Journal of comparative neurology.

[56]  C. Gerday,et al.  Monoclonal antibodies directed against the calcium binding protein parvalbumin. , 1988, Cell calcium.

[57]  F. Wouterlood,et al.  Hippocampal and midline thalamic fibers and terminals in relation to the choline acetyltransferase‐immunoreactive neurons in nucleus accumbens of the rat: A light and electron microscopic study , 1990, The Journal of comparative neurology.

[58]  O. Manzoni,et al.  Nitric oxide-induced blockade of NMDA receptors , 1992, Neuron.

[59]  H. Parthasarathy,et al.  Local Release of GABAergic Inhibition in the Motor Cortex Induces Immediate-Early Gene Expression in Indirect Pathway Neurons of the Striatum , 1997, The Journal of Neuroscience.

[60]  K. Akert,et al.  A stereotaxic atlas of the brain of the squirrel monkey : (Saimiri sciureus) , 1963 .

[61]  Charles J. Wilson,et al.  Striatal interneurones: chemical, physiological and morphological characterization , 1995, Trends in Neurosciences.

[62]  P. Somogyi,et al.  Fine structural studies on a type of somatostatin‐immurioreactive neuron and its synaptic connections in the rat neostriatum: A correlated light and electron microscopic study , 1983, The Journal of comparative neurology.

[63]  E. Reynolds THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY , 1963, The Journal of cell biology.

[64]  S. Consolo,et al.  The Cerebral Cortex and Parafascicular Thalamic Nucleus Facilitate In vivo Acetylcholine Release in the Rat Striatum through Distinct Glutamate Receptor Subtypes , 1996, The European journal of neuroscience.

[65]  D. Surmeier,et al.  Muscarinic receptors modulate N-, P-, and L-type Ca2+ currents in rat striatal neurons through parallel pathways , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[66]  A. Nieoullon,et al.  Striatal neuropeptide Y neurones are not a target for thalamic afferent fibres. , 1996, Neuroreport.

[67]  A. Parent,et al.  Efferent connections of the centromedian and parafascicular thalamic nuclei in the squirrel monkey: A PHA‐L study of subcortical projections , 1992, The Journal of comparative neurology.

[68]  C. Wilson,et al.  Projection subtypes of rat neostriatal matrix cells revealed by intracellular injection of biocytin , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[69]  M. Difiglia Synaptic organization of cholinergic neurons in the monkey neostriatum , 1987, The Journal of comparative neurology.

[70]  A. D. Smith,et al.  The neural network of the basal ganglia as revealed by the study of synaptic connections of identified neurones , 1990, Trends in Neurosciences.

[71]  A. Hendrickson,et al.  Transient co-localization of calretinin, parvalbumin, and calbindin-D28k in developing visual cortex of monkey , 1995, Journal of neurocytology.

[72]  Charles J. Wilson,et al.  Surround inhibition among projection neurons is weak or nonexistent in the rat neostriatum. , 1994, Journal of neurophysiology.

[73]  J. Bolam,et al.  Input from the frontal cortex and the parafascicular nucleus to cholinergic interneurons in the dorsal striatum of the rat , 1992, Neuroscience.

[74]  A. Graybiel,et al.  Responses of tonically active neurons in the primate's striatum undergo systematic changes during behavioral sensorimotor conditioning , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[75]  A. Reiner,et al.  Calretinin is largely localized to a unique population of striatal interneurons in rats , 1996, Brain Research.

[76]  J. Rogers,et al.  Calretinin in rat brain: An immunohistochemical study , 1992, Neuroscience.

[77]  S. Consolo,et al.  The parafascicular thalamic nucleus modulates messenger RNA encoding glutamate decarboxylase 67 in rat striatum , 1997, Neuroscience.

[78]  S. T. Kitai,et al.  Medium spiny neuron projection from the rat striatum: An intracellular horseradish peroxidase study , 1980, Brain Research.

[79]  T. Hökfelt,et al.  Coexistence of somatostatin- and avian pancreatic polypeptide (APP)-like immunoreactivity in some forebrain neurons , 1982, Neuroscience.