Projection from the cerebellar lateral nucleus to precerebellar nuclei in the mossy fiber pathway is glutamatergic: A study combining anterograde tracing with immunogold labeling in the rat
Corresponding Author
Cornelius Schwarz
Sektion für Visuelle Sensomotorik, Neurologische Universitätsklinik Tübingen, 72076 Tübingen, Germany
Sektion für visuelle Sensomotorik, Neurologische Universitätsklinik Tübingen, Hoppe-Seyler Strasse 3, 72076 Tübingen, GermanySearch for more papers by this authorYvonne Schmitz
Sektion für Visuelle Sensomotorik, Neurologische Universitätsklinik Tübingen, 72076 Tübingen, Germany
Search for more papers by this authorCorresponding Author
Cornelius Schwarz
Sektion für Visuelle Sensomotorik, Neurologische Universitätsklinik Tübingen, 72076 Tübingen, Germany
Sektion für visuelle Sensomotorik, Neurologische Universitätsklinik Tübingen, Hoppe-Seyler Strasse 3, 72076 Tübingen, GermanySearch for more papers by this authorYvonne Schmitz
Sektion für Visuelle Sensomotorik, Neurologische Universitätsklinik Tübingen, 72076 Tübingen, Germany
Search for more papers by this authorAbstract
The pontine nuclei (PN) and the nucleus reticularis tegmenti pontis (NRTP) are sources of an excitatory projection to the cerebellar cortex via mossy fibers and a direct excitatory projection to the cerebellar nuclei. These precerebellar nuclei, in turn, receive a feedback projection from the cerebellar nuclei, which mostly originate in the lateral nucleus (LN). It has been suggested that the feedback projection from the LN partially uses γ-aminobutyric acid (GABA) as a transmitter. We tested this hypothesis by using a combination of anterograde tracing (biotinylated dextran amine injection into the LN) and postembedding GABA and glutamate immunogold histochemistry. The pattern of labeling in the PN and the NRTP was compared with that of cerebellonuclear terminals in two other target structures, the parvocellular part of the nucleus ruber (RNp) and the ventromedial and ventrolateral thalamus (VM/VL). The projection to the inferior olive (IO), which is known to be predominantly GABAergic, served as a control. A quantitative analysis of the synaptic terminals labeled by the tracer within the PN, the NRTP, and the VL/VM revealed no GABA immunoreactivity. Only one clearly labeled terminal was found in the RNp. In contrast, 72% of the terminals in the IO were clearly GABA immunoreactive, confirming the reliability of our staining protocol. Correspondingly, glutamate immunohistochemistry labeled the majority of the cerebellonuclear terminals in the PN (88%), the NRTP (90%), the RNp (93%), and the VM/VL (63%) but labeled only 5% in the IO. These data do not support a role for GABAergic inhibition either in the feedback systems from the LN to the PN and the NRTP or within the projections to the RNp and the VM/VL. J. Comp. Neurol. 381:320-334, 1997. © 1997 Wiley-Liss, Inc.
Literature Cited
- Aas, J.-E., and P. Brodal (1990) GABA and glycine as putative transmitters in subcortical pathways to the pontine nuclei. A combined immunocytochemical and retrograde tracing study in the cat with some observations in the rat. Neuroscience 34: 149–162.
- Angaut, P., and F. Cicirata (1988) The dentatorubral projection in the rat: An autoradiographic study. Behav. Brain Res. 28: 71–73.
- Angaut, P., and C. Sotelo (1987) The dentato-olivary projection in the rat as a presumptive GABAergic link in the olivo-cerebello-olivary loop. An ultrastructural study. Neurosci. Lett. 83: 227–231.
- Angaut, P., and C. Sotelo (1989) Synaptology of the cerebello-olivary pathway. Double labelling with anterograde axonal tracing and GABA immunocytochemistry in the rat. Brain Res. 479: 361–365.
- Angaut, P., F. Cicirata, and M. F. Serapide (1985) Topographic organization of the cerebellothalamic projections in the rat. An autoradiographic study. Neuroscience 15: 389–401.
- Angaut, P., C. Batini, J. M. Billard, and H. Daniel (1986) The cerebellorubral projection in the rat: Retrograde anatomical study. Neurosci. Lett. 68: 63–68.
- Asanuma, C., W. T. Thach, and E. G. Jones (1983) Distribution of cerebellar terminations and their relation to other afferent terminations in the ventral lateral thalamic region of the monkey. Brain Res. Rev. 5: 237–265.
- Aumann, T. D., J. A. Rawson, D. I. Finkelstein, and M. K. Horne (1994) Projections from the lateral and interposed cerebellar nuclei to the thalamus of the rat: A light and electron microscopic study using single and double anterograde labelling. J. Comp. Neurol. 349: 165–181.
- Azizi, S. A., G. A. Mihailoff, R. A. Burne, and D. J. Woodward (1981) The pontocerebellar system in the rat: An HRP study. I. Posterior vermis. J. Comp. Neurol. 197: 543–558.
- Beitz, A. J. (1976) The topographical organization of the olivo-dentate and dentato-olivary pathways in the cat. Brain Res. 115: 311–317.
- Berreta, S., G. Bosco, G. Giaquinta, G. Smecca, and V. Perciavalle (1993) Cerebellar influences on accessory oculomotor nuclei of the rat: A neuroanatomical, immunohistochemical, and electrophysiological study. J. Comp. Neurol. 338: 50–66.
- Border, B. G., and G. A. Mihailoff (1991) Glutamate immunoreactivity in the rat basilar pons: Light and electron microscopy reveals labeled boutons and cells of origin of afferent projection. Neuroscience 45: 47–61.
- Border, B. G., R. J. Kosinski, S. A. Azizi, and G. A. Mihailoff (1986) Certain basilar pontine afferent systems are GABA-ergic: Combined HRP and immunocytochemical studies in the rat. Brain Res. Bull. 17: 169–179.
- Bower, J. M., D. H. Beermann, J. M. Gibson, G. M. Shambes, and W. Welker (1981) Principles of organization of a cerebro-cerebellar circuit. Brain Behav. Evol. 18: 1–18.
- Brodal, A., and G. Szikla (1972) The termination of the brachium conjunctivum descendens in the nucleus reticularis tegmenti pontis. Brain Res. 39: 337–351.
- Brodal, A., J. Destombes, A. M. Lacerda, and P. Angaut (1972a) A cerebellar projection onto the pontine nuclei. An experimental anatomical study in the cat. Exp. Brain Res. 16: 115–139.
- Brodal, A., A. M. Lacerda, J. Destombes, and P. Angaut (1972b) The pattern in the projection of the intracerebellar nuclei onto the nucleus reticularis tegmenti pontis in the cat. An experimental anatomical study. Exp. Brain Res. 16: 140–160.
- Brodal, P. (1968a) The corticopontine projection in the cat. Demonstration of a somatotopically organized projection from the second somatosensory cortex. Arch. Ital. Biol. 106: 310–322.
- Brodal, P. (1968b) The corticopontine projection in the cat. I. Demonstration of a somatotopically organized projection from the primary sensorimotor cortex. Exp. Brain Res. 5: 210–234.
- Brodal, P. (1978) The corticopontine projection in the rhesus monkey. Origin and principles of organization. Brain 101: 251–283.
- Caughell, K. A., and B. A. Flumerfelt (1977) The organization of the cerebellorubral projection: An experimental study in the rat. J. Comp. Neurol. 176: 295–306.
-
Chan-Palay, V.
(1977)
Cerebellar Dentate Nucleus.
Berlin:
Springer-Verlag.
10.1007/978-3-642-66498-4 Google Scholar
- Courville, J., J. R. Augustine, and P. Martel (1977) Projections from the inferior olive to the cerebellar nuclei in the cat demonstrated by retrograde transport of horseradish peroxidase. Brain Res. 130: 405–419.
- Davies, J., A. J. Miller, and M. J. Sheardown (1986) Amino acid mediated excitatory synaptic transmission in the cat red nucleus. J. Physiol. 376: 13–29.
- De Zeeuw, C. I., and T. J. H. Ruigrok (1994) Olivary projecting neurons in the nucleus of Darkschewitsch in the cat receive excitatory monosynaptic input from the cerebellar nuclei. Brain Res. 653: 345–350.
- De Zeeuw, C. I., J. C. Holstege, F. Calkoen, T. J. H. Ruigrok, and J. Voogd (1988) A new combination of WGA-HRP anterograde tracing and GABA immunocytochemistry applied to afferents of the cat inferior olive at the ultrastructural level. Brain Res. 447: 369–375.
- De Zeeuw, C. I., J. C. Holstege, T. J. H. Ruigrok, and J. Voogd (1989) Ultrastructural study of the GABAergic, cerebellar and mesodiencephalic innervation of the cat medial accessory olive: Anterograde tracing combined with immunocytochemistry. J. Comp. Neurol. 284: 12–35.
- Faull, R. L. M., and J. B. Carman (1978) The cerebellofugal projections in the brachium conjunctivum of the rat. I. The contralateral ascending pathway. J. Comp. Neurol. 178: 495–518.
- Flumerfelt, B. A., S. Otabe, and J. Courville (1973) Distinct projection to the red nucleus from the dentate and interposed nuclei in the monkey. Brain Res. 50: 408–414.
- Giuffrida, R., G. Aicardi, A. Canedi, and C. Rapisarda (1993) Excitatory amino acids as neurotransmitters of cortical and cerebellar projections to the red nucleus: An immunocytochemical study in the guinea pig. Somatosens. Motor Res. 10: 365–376.
-
Gorodnov, V. L., and
V. V. Fanardjian
(1987)
Functional properties of the cerebellorubral synapses in the cat.
Brain Res.
410:
340–342.
10.1016/0006-8993(87)90334-9 Google Scholar
- Gray, E. G. (1959) Axo-somatic and axo-dendritic synapses of the cerebral cortex: An electron microscopic study. J. Anat. 93: 420–433.
- Haroian, A. J., L. C. Massopust, and P. A. Young (1981) Cerebellothalamic projections in the rat: An autoradiographic and degeneration study. J. Comp. Neurol. 197: 217–236.
- Hellstrøm-Hoddevik, G. (1978) The projection from nucleus reticularis tegmenti pontis onto the cerebellum in the cat. Anat. Embryol. 153: 227–242.
- Hendry, S. H. C., E. G. Jones, and J. Graham (1979) Thalamic relay nuclei for cerebellar and certain related fiber systems in the cat. J. Comp. Neurol. 185: 679–714.
- Holstege, G., and J. Tan (1988) Projections from the red nucleus and surrounding areas to the brainstem and spinal cord in the cat. An HRP and autoradiographical tracing study. Behav. Brain Res. 28: 33–57.
- Ito, M., M. Yoshida, K. Obata, N. Kawai, and M. Udo (1970) Inhibitory control of intracerebellar nuclei by the Purkinje cell axons. Exp. Brain Res. 10: 64–80.
- Kalil, K. (1981) Projections of the cerebellar and dorsal column nuclei upon the thalamus of the rhesus monkey. J. Comp. Neurol. 195: 25–50.
- Keifer, J., and J. C. Houk (1991) Role of excitatory amino acids in mediating burst discharge of red nucleus neurons in the in vitro turtle brain stem-cerebellum. J. Neurophysiol. 65: 454–467.
- Kitai, S. T., J. D. Kocsis, and T. Kiyohara (1976) Electrophysiological properties of nucleus reticularis tegmenti pontis cells: Antidromic and synaptic activation. Exp. Brain Res. 24: 295–309.
- Kumoi, K., N. Saito, T. Kuno, and C. Tanaka (1988) Immunohistochemical localization of α-aminobutyric acid- and aspartate-containing neurons in the rat deep cerebellar nuclei. Brain Res. 439: 302–310.
- Legendre, A., and J. Courville (1987) Origin and trajectory of the cerebelloolivary projection: An experimental study with radioactive and fluorescent tracers in the cat. Neuroscience 21: 877–891.
- Madl, J. E., A. A. Larson, and A. J. Beitz (1986) Monoclonal antibody specific for carbodiimide-fixed glutamate: Immunocytochemical localization in the rat CNS. J. Histochem. Cytochem. 34: 317–326.
- MadI, J. E., A. J. Beitz, R. L. Johnson, and A. A. Larson (1987) Monoclonal antibodies specific for fixative-modified aspartate: Immunocytochemi-cal localization in the rat CNS. J. Neurosci. 7: 2639–2650.
- Martin, G. F. (1973) Projections of the cerebellum to the precerebellar relay nuclei in the opossum. Anat. Rec. 175: 384.
- Martin, G. F., C. K. Henkel, and J. S. King (1976) Cerebello-olivary fibers: Their origin, course and distribution in the north american opossum. Exp. Brain Res. 24: 219–236.
- Mihailoff, G. A. (1993) Cerebellar nuclear projections from the basilar pontine nuclei and nucleus reticularis tegmenti pontis as demonstrated with PHA-L tracing in the rat. J. Comp. Neurol. 330: 130–146.
- Mihailoff, G. A. (1994) Identification of pontocerbellar axon collateral synatpic boutons in the rat cerebellar nuclei. Brain Res. 648: 313–318.
- Mihailoff, G. A., R. A. Burne, S. A. Azizi, G. Norell, and D. J. Woodward (1981) The pontocerebellar system in the rat: An HRP study. II. Hemispheral components. J. Comp. Neurol. 197: 559–577.
- Monaghan, P. L., A. J. Beitz, A. A. Larson, R. A. Altschuler, J. E. Madl, and M. A. Mullett (1986) Immunocytochemical localization of glutamate-glutaminase-, and aspartate aminotransferase-like immunoreactivity in the rat deep cerebellar nuclei. Brain Res. 363: 364–370.
- Nikundiwe, A. M., J. G. Bjaalie, and P. Brodal (1994) Lamellar organization of pontocerebellar neuronal populations. A multi-tracer and 3-D computer reconstruction study in the cat. Eur. J. Neurosci. 6: 173–186.
- Oka, H. (1988) Functional organization of the parvocellular red nucleus in the cat. Behav. Brain Res. 28: 233–240.
- Orioli, P. J., and P. L. Strick (1989) Cerebellar connections with the motor cortex and the arcuate premotor area: An analysis employing retrograde transneuronal transport of WGA-HRP. J. Comp. Neurol. 288: 612–626.
- Ruigrok, T. J. H., and J. Voogd (1995) Cerebellar influence on olivary excitability in the cat. Eur. J. Neurosci. 7: 679–693.
- Sakaguchi, H., M. Kubota, M. Nakamura, and N. Tsukahara (1984) Effects of amino acids on cat red nucleus neurons in vitro. Exp. Brain Res. 54: 150–156.
- Schwarz, C., and P. Thier (1995) Modular organization of the pontine nuclei: Dendritic fields of identified pontine projection neurons in the rat respect the borders of cortical afferent fields. J. Neurosci. 15: 3475–3489.
- Shinoda, Y., T. Futami, and M. Kano (1985) Synaptic organization of the cerebello-thalamo-cerebral pathway in the cat. II. Input-output organization of single thalamocortical neurons in the ventrolateral thalamus. Neurosci. Res. 2: 157–180.
- Shinoda, Y., Y. Sugiuchi, and T. Futami (1987) Excitatory inputs to cerebellar dentate nucleus neurons from the cerebral cortex in the cat. Exp. Brain Res. 67: 299–315.
- Shinoda, Y., Y. Sugiuchi, T. Futami, and R. Izawa (1992) Axon collaterals of mossy fibers from the pontine nucleus in the cerebellar dentate nucleus. J. Neurophysiol. 67: 547–560.
- Shinoda, Y., T. Futami, and S. Kakei (1993) Input-output organization of the ventrolateral nucleus of the thalamus. Stereotact. Funct. Neurosurg. 60: 17–31.
- Stanton, G. B. (1980) Topographical organization of ascending cerebellar projections from the dentate and interposed nuclei in Macaca mulatta: An anterograde degeneration study. J. Comp. Neurol. 190: 699–731.
- Strominger, N. L., T. C. Truscott, R. A. Miller, and G. J. Royce (1979) An autoradiographic study of the rubroolivary tract in the rhesus monkey. J. Comp. Neurol. 183: 33–46.
- Thielert, C.-D., and P. Thier (1993) Patterns of projections from the pontine nuclei and the nucleus reticularis tegmenti pontis to the posterior vermis in the rhesus monkey: A study using retrograde tracers. J. Comp. Neurol. 337: 113–126.
- Tolbert, D. L., L. C. Massopust, M. G. Murphy, and P. A. Young (1976) The anatomical organization of the cerebello-olivary projection in the cat. J. Comp. Neurol. 170: 525–544.
- Toyama, K., N. Tsukahara, and M. Udo (1968) Nature of the cerebellar influences upon the red nucleus neurones. Exp. Brain Res. 4: 292–309.
- Toyama, K., N. Tsukahara, K. Kosaka, and K. Matsunami (1970) Synaptic excitation of red nucleus neurones by fibres from interpositus nucleus. Exp. Brain Res. 11: 187–198.
- Tsukahara, N., and T. Bando (1970) Red nuclear and interposate nuclear excitation of pontine nuclear cells. Brain Res. 19: 295–298.
- Tsukahara, N., H. Korn, and J. Stone (1968) Pontine relay from cerebral cortex to cerebellar cortex and nucleus interpositus. Brain Res. 10: 448–453.
- Tsukahara, N., T. Bando, S. T. Kitai, and T. Kiyohara (1971) Cerebellopontine reverberating circuit. Brain Res. 33: 233–237.
- Uno, M., M. Yoshida, and I. Hirota (1970) The mode of cerebello-thalamic relay transmission investigated with intracellular recording from cells of the ventrolateral nucleus of cat's thalamus. Exp. Brain Res. 10: 121–139.
- Watt, C. B., and G. A. Mihailoff (1983) The cerebellopontine system in the rat. I. Autoradiographic studies. J. Comp. Neurol. 215: 312–330.
- Wiesendanger, R., and M. Wiesendanger (1982) The corticopontine system in the rat. II. The projection pattern. J. Comp. Neurol. 208: 227–238.
- Wiesendanger, R., and M. Wiesendanger (1985) Cerebello-cortical linkage in the monkey as revealed by transcellular labeling with the lectin wheat germ agglutinin conjugated to the marker horseradish peroxidase. Exp. Brain Res. 59: 105–117.
- Wouterlood, F. G., and B. Jorritsma-Byham (1993) The anterograde neuroanatomical tracer biotinylated dextran-amine: Comparison with the tracer Phaseolus vulgaris-leucagglutinin in preparations for electron microscopy. J. Neurosci. Methods 48: 75–87.
- Yamamoto, T., Y. Kishimoto, H. Yoshikawa, and H. Oka (1991) Intracellular recordings from rat thalamic VL neurons: A study combined with intracellular staining. Exp. Brain Res. 87: 245–253.
- Yuen, H., R. M. Dom, and G. F. Martin (1974) Cerebellopontine projections in the American opossum. A study of their origin, distribution and overlap with fibers from the cerebral cortex. J. Comp. Neurol. 154: 237–286.