Skip to main content
Log in

Spinocerebellar ataxias types 2 and 3: degeneration of the precerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum

  • Published:
Journal of Neural Transmission Aims and scope Submit manuscript

Summary.

The precerebellar nuclei act as a gate for the entire neocortical, brainstem and spinal cord afferent input destined for the cerebellum. Since no pathoanatomical studies of these nuclei had yet been performed in spinocerebellar ataxia type 2 (SCA2) or type 3 (SCA3), we carried out a detailed postmortem study of the precerebellar nuclei in six SCA2 and seven SCA3 patients in order to further characterize the extent of brainstem degeneration in these ataxic disorders. By means of unconventionally thick serial sections through the brainstem stained for lipofuscin pigment and Nissl material, we could show that all of the precerebellar nuclei (red, pontine, arcuate, prepositus hypoglossal, superior vestibular, lateral vestibular, medial vestibular, interstitial vestibular, spinal vestibular, vermiform, lateral reticular, external cuneate, subventricular, paramedian reticular, intercalate, interfascicular hypoglossal, and conterminal nuclei, pontobulbar body, reticulotegmental nucleus of the pons, inferior olive, and nucleus of Roller) are among the targets of both of the degenerative processes underlying SCA2 and SCA3. These novel findings are in contrast to the current neuropathological literature, which assumes that only a subset of precerebellar nuclei in SCA2 and SCA3 may undergo neurodegeneration. Widespread damage to the precerebellar nuclei separates all three phylogenetically and functionally defined regions of the cerebellum, impairs their physiological functions and thus explains the occurrence of gait, stance, limb and truncal ataxia, dysarthria, truncal and postural instability with disequilibrium, impairments of the vestibulo-ocular reaction and optokinetic nystagmus, slowed and saccadic smooth pursuits, dysmetrical horizontal saccades, and gaze-evoked nystagmus during SCA2 and SCA3.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • M Abele K Bürk F Andres H Topka F Laccone S Bosch A Brice G Cancel J Dichgans T Klockgether (1997) ArticleTitleAutosomal dominant cerebellar ataxia type. I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3. Brain 120 2141–2148 Occurrence Handle10.1093/brain/120.12.2141 Occurrence Handle9448569

    Article  PubMed  Google Scholar 

  • Alexander GE, DeLong MR (1992) Central mechanisms of initiation and control of movement. In: Asbury AK, McKhann GM, McDonald WI (eds) Diseases of the nervous system: clinical neurobiology, 2nd edn. Saunders, Philadelphia, pp 285–308

  • G Auburger G Orozoco R Ferreira S Gispert M Paradoa M Estrada M Garcia M Farall R Williamson S Chamberlain L Heredero (1990) ArticleTitleAutosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population. Am J Hum Genet 46 1163–1177 Occurrence Handle1971152

    PubMed  Google Scholar 

  • NH Barmack (2003) ArticleTitleCentral vestibular system and posterior cerebellum. Brain Res Bull 60 511–541 Occurrence Handle10.1016/S0361-9230(03)00055-8 Occurrence Handle12787870

    Article  PubMed  Google Scholar 

  • H Braak (1970a) ArticleTitleNuclei of the human brain stem. I. Inferior olive, conterminal nucleus and vermiform nucleus of the restiform body. Z Zellforsch Mikrosk Anat 105 442–456 Occurrence Handle10.1007/BF00335466

    Article  Google Scholar 

  • H Braak (1970b) ArticleTitleOn the nuclei of the human brain stem. II. The raphe nuclei. Z Zellforsch Mikrosk Anat 107 123–141 Occurrence Handle10.1007/BF00338964

    Article  Google Scholar 

  • H Braak (1971) ArticleTitleNuclei of the human brain stem. IV. Nucleus reticularis lateralis and its satellites. Z Zellforsch Mikrosk Anat 122 145–159 Occurrence Handle10.1007/BF00337626 Occurrence Handle4107629

    Article  PubMed  Google Scholar 

  • H Braak E Braak (1991) ArticleTitleDemonstration of amyloid deposits and neurofibrillary changes in whole brain sections. Brain Pathol 1 213–216 Occurrence Handle1669710

    PubMed  Google Scholar 

  • H Braak E Braak (1998) ArticleTitleInvolvement of the precerebellar nuclei in Pick’s disease. Exp Neurol 153 351–365 Occurrence Handle10.1006/exnr.1998.6895 Occurrence Handle9784294

    Article  PubMed  Google Scholar 

  • H Braak U Rüb K Del Tredici (2003) ArticleTitleInvolvement of precerebellar nuclei in multiple system atrophy. Neuropathol Appl Neurobiol 29 60–76 Occurrence Handle10.1046/j.1365-2990.2003.00432.x Occurrence Handle12581341

    Article  PubMed  Google Scholar 

  • K Bürk M Fetter M Abele F Laccone A Brice J Dichgans T Klockgether (1999) ArticleTitleAutosomal dominant cerebellar ataxia type I. Oculomotor abnormalities in families with SCA1, SCA2, and SCA3. J Neurol 246 789–797 Occurrence Handle10.1007/s004150050456 Occurrence Handle10525976

    Article  PubMed  Google Scholar 

  • JA Büttner-Ennever U Büttner (1992) ArticleTitleNeuroanatomy of the ocular motor pathways. Baillières Clin Neurol 1 263–287 Occurrence Handle1344070

    PubMed  Google Scholar 

  • A Dürr D Smadja G Cancel A Lezin G Stevanin J Mikol R Bellance GG Buisson H Chneiweiss J Dellanave Y Agid A Brice JC Vernant (1995) ArticleTitleAutosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families. Brain 118 1573–1581 Occurrence Handle8595486

    PubMed  Google Scholar 

  • A Dürr G Stevanin G Cancel C Duyckaerts N Abbas O Didierjean H Chneiweiss A Benomar O Lyon-Caen J Julien M Serdaru C Penet Y Agid A Brice (1996) ArticleTitleSpinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular and neuropathological features. Ann Neurol 39 490–499 Occurrence Handle10.1002/ana.410390411 Occurrence Handle8619527

    Article  PubMed  Google Scholar 

  • R Estrada J Galarraga G Orozco A Nodarse G Auburger (1999) ArticleTitleSpinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies. Acta Neuropathol 97 306–310 Occurrence Handle10.1007/s004010050989 Occurrence Handle10090679

    Article  PubMed  Google Scholar 

  • VG Evidente KA Gwinn-Hardy JN Caviness S Gilman (2000) ArticleTitleHereditary ataxias. Mayo Clin Proc 75 475–490 Occurrence Handle10807077

    PubMed  Google Scholar 

  • Gerrits NM (1990) Vestibular nuclear complex. In: Paxinos G (ed) The human central nervous system. Academic Press, San Diego, pp 863–888

  • Ghez C (1991) The cerebellum. In: Kandel ER, Schwartz JH, Jessell TM (eds) Principles of neural science. Elsevier, New York, pp 626–646

  • Gilman S (1992) Cerebellum and motor dysfunction. In: Asbury AK, McKhann GM, McDonald WI (eds) Diseases of the nervous system: clinical neurobiology, 2nd edn. Saunders, Philadelphia, pp 368–389

  • S Gilman (2000) ArticleTitleThe spinocerebellar ataxias. Clin Neuropharmacol 23 296–303 Occurrence Handle10.1097/00002826-200011000-00002 Occurrence Handle11575863

    Article  PubMed  Google Scholar 

  • CR Gordon V Joffe G Vainstein N Gadoth (2003) ArticleTitleVestibulo-ocular arreflexia in families with spinocerebellar ataxia type 3 (Machado-Joseph disease). J Neurol Neurosurg Psychiatry 74 1403–1406 Occurrence Handle10.1136/jnnp.74.10.1403 Occurrence Handle14570834

    Article  PubMed  Google Scholar 

  • Horn AKE, Büttner U, Büttner-Ennever JA (1999) Brainstem and cerebellar structures for eye movement generation. In: Büttner U (ed) Vestibular dysfunction and its therapy. Karger, Basel, pp 1–25

  • DP Huynh MR Del Bigio DH Ho SM Pulst (1999) ArticleTitleExpression of ataxin-2 in brains from normal individuals and patients with Alzheimer’s disease and spinocerebellar ataxia 2. Ann Neurol 45 232–241 Occurrence Handle10.1002/1531-8249(199902)45:2<232::AID-ANA14>3.0.CO;2-7 Occurrence Handle9989626

    Article  PubMed  Google Scholar 

  • DP Huynh K Figueroa N Hoang SM Pulst (2000) ArticleTitleNuclear localization of inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human. Nat Genet 26 44–50 Occurrence Handle10.1038/79162 Occurrence Handle10973246

    Article  PubMed  Google Scholar 

  • G Imbert F Saudou G Yvert D Devys Y Trottier JM Garnier C Weber JL Mandel G Cancel N Abbas A Dürr O Didierjean G Stevanin Y Agid A Brice (1996) ArticleTitleCloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats. Nat Genet 14 285–291 Occurrence Handle10.1038/ng1196-285 Occurrence Handle8896557

    Article  PubMed  Google Scholar 

  • K Iwabuchi K Tsuchiya T Uchihara S Yagishita (1999) ArticleTitleAutosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations. Rev Neurol 155 255–270 Occurrence Handle10367323

    PubMed  Google Scholar 

  • Jones EG (1985) The thalamus. Plenum Press, New York

  • T Kanda E Isozaki S Kato H Tanabe M Oda (1989) ArticleTitleType III Machado-Joseph disease in a Japanese family: a clinicopathological study with special reference to the peripheral nervous system. Clin Neuropathol 8 134–141 Occurrence Handle2743650

    PubMed  Google Scholar 

  • Y Kawaguchi T Okamoto M Taniwaki M Aizawa M Inoue S Katayama H Kawakami S Nakamura M Nishimura I Akiguchi J Kimura S Narumiya A Kazizuka (1994) ArticleTitleCAG expansion in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat Genet 8 221–228 Occurrence Handle10.1038/ng1194-221 Occurrence Handle7874163

    Article  PubMed  Google Scholar 

  • Klockgether T (2003) Ataxias. In: Goetz CG (ed) Textbook of clinical neurology, 2nd edn. WB Saunders, Philadelphia, pp 741–757

  • Leigh RJ, Zee DS (1991) The neurology of eye movements, 2nd edn. Davis, Philadelphia

  • Mizusawa H, Clark HB, Koeppen AH (2003) Spinocerebellar ataxias. In: Dickson D (ed) Neurodegeneration: the molecular pathology of dementia and movement disorders. The International Society of Neuropathology Press, Basel, pp 242–256

  • Olszewski J, Baxter D (1982) Cytoarchitecture of the human brain stem, 2nd edn. Karger, Basel

  • JT Pang P Giunti S Chamberlain SF An R Vitaliani T Scaravilli L Martinian NW Wood F Scaravilli O Ansorge (2002) ArticleTitleNeuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases. Brain 125 656–663 Occurrence Handle10.1093/brain/awf060 Occurrence Handle11872620

    Article  PubMed  Google Scholar 

  • H Paulson Z Ammache (2001) ArticleTitleAtaxia and hereditary disorders. Neurol Clin 19 759–782 Occurrence Handle10.1016/S0733-8619(05)70044-X Occurrence Handle11532653

    Article  PubMed  Google Scholar 

  • HL Paulson (2000) ArticleTitleToward an understanding of polyglutamine neurodegeneration. Brain Pathol 10 293–299 Occurrence Handle10764049

    PubMed  Google Scholar 

  • Paxinos G, Törk I, Halliday G, Mehler WR (1990) Human homologs to brainstem nuclei identified in other animals as revealed by acetylcholinesterase activity. In: Paxinos G (ed) The human central nervous system. Academic Press, San Diego, pp 149–202

  • SM Pulst A Nechiporuk T Nechiporuk S Gispert XN Chen I Lopes-Cendes S Pearlman S Starkman G Orozco-Diaz A Lunkes P DeJong GA Rouleau G Auburger JR Korenberg C Figueroa S Sahba (1996) ArticleTitleModerate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nat Genet 14 269–276 Occurrence Handle10.1038/ng1196-269 Occurrence Handle8896555

    Article  PubMed  Google Scholar 

  • O Riess FA Laccone S Gispert L Schöls C Zühlke AM Vieira-Saecker S Herlt K Wessel JT Epplen BH Weber F Kreuz S Chahrokh-Zadeh A Meindl A Lunkes J Aguiar M Macek SuffixJr A Krebsova M Macek SuffixSr K Bürk S Tinschert I Schreyer SM Pulst G Auburger (1997) ArticleTitleSCA2 trinucleotide expansion in German SCA2 patients. Neurogenetics 1 59–64 Occurrence Handle10.1007/s100480050009 Occurrence Handle10735276

    Article  PubMed  Google Scholar 

  • Y Robitaille I Lopes-Cendes M Becher G Rouleau AW Clark (1997) ArticleTitleThe neuropathology of CAG repeat diseases: review and update of genetic and molecular features. Brain Pathol 7 901–926 Occurrence Handle9217975

    PubMed  Google Scholar 

  • U Rüb K Del Tredici C Schultz DR Thal E Braak H Braak (2000) ArticleTitleThe evolution of Alzheimer’s disease-related cytoskeletal pathology in the human raphe nuclei. Neuropathol Appl Neurobiol 26 553–567 Occurrence Handle10.1046/j.0305-1846.2000.00291.x Occurrence Handle11123722

    Article  PubMed  Google Scholar 

  • U Rüb C Schultz K Del Tredici H Braak (2001) ArticleTitleEarly involvement of the tegmentopontine reticular nucleus during the evolution of Alzheimer’s disease-related cytoskeletal pathology. Brain Res 908 107–112 Occurrence Handle10.1016/S0006-8993(01)02598-7 Occurrence Handle11454320

    Article  PubMed  Google Scholar 

  • U Rüb RAI de Vos ER Brunt C Schultz K Del Tredici H Paulson H Braak (2002a) ArticleTitleDegeneration of the external cuneate nucleus in spinocerebellar ataxia type 3 (Machado-Joseph disease). Brain Res 953 126–134 Occurrence Handle10.1016/S0006-8993(02)03278-X

    Article  Google Scholar 

  • U Rüb RAI de Vos C Schultz ER Brunt H Paulson H Braak (2002b) ArticleTitleSpinocerebellar ataxia type 3 (Machado-Joseph disease): severe destruction of the lateral reticular nucleus. Brain 125 2115–2124 Occurrence Handle10.1093/brain/awf208

    Article  Google Scholar 

  • U Rüb ER Brunt D Del Turco RAI de Vos K Gierga H Paulson H Braak (2003a) ArticleTitleGuidelines for the pathoanatomical examination of the lower brain stem in ingestive and swallowing disorders and its application to a dysphagic spinocerebellar ataxia type 3 patient. Neuropathol Appl Neurobiol 29 1–13 Occurrence Handle10.1046/j.1365-2990.2003.00437.x

    Article  Google Scholar 

  • U Rüb D Del Turco K Del Tredici RA de Vos ER Brunt G Reifenberger C Seifried C Schultz G Auburger H Braak (2003b) ArticleTitleThalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance. Brain 126 2257–2272 Occurrence Handle10.1093/brain/awg234

    Article  Google Scholar 

  • U Rüb C Schultz K Del Tredici K Gierga G Reifenberger RA de Vos C Seifried H Braak G Auburger (2003c) ArticleTitleAnatomically-based guidelines for systematic investigations of the central somatosensory system and their application to a spinocerebellar ataxia type 2 (SCA2) patient. Neuropathol Appl Neurobiol 29 418–433 Occurrence Handle10.1046/j.1365-2990.2003.00504.x

    Article  Google Scholar 

  • U Rüb ER Brunt RAI de Vos D Del Turco K Del Tredici K Gierga C Schultz E Ghebremedhin K Bürk G Auburger H Braak (2004a) ArticleTitleDegeneration of the central vestibular system in spinocerebellar ataxia type 3 patients and its possible clinical significance. Neuropathol Appl Neurobiol 30 402–414 Occurrence Handle10.1111/j.1365-2990.2004.00554.x

    Article  Google Scholar 

  • U Rüb K Bürk L Schöls ER Brunt RAI de Vos G Orozco Diaz K Gierga E Ghebremedhin C Schultz D Del Turco M Mittelbronn G Auburger T Deller H Braak (2004b) ArticleTitleDamage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3. Neurology 63 1258–1263

    Google Scholar 

  • Rüb U, Del Turco D, Bürk K, Orozco Diaz G, Auburger G, Mittelbronn M, Gierga K, Ghebremedhin E, Schultz C, Schöls L, Bohl J, Braak H, Deller T (2004c) Extended pathoanatomical studies point to a consistent affection of the thalamus in spinocerebellar ataxia type 2. Neuropathol Appl Neurobiol (in press)

  • T Schmidt GB Landwehrmeyer I Schmitt Y Trottier G Auburger F Laccone T Klockgether M Volpel JT Epplen L Schöls O Riess (1998) ArticleTitleAn isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients. Brain Pathol 8 669–679 Occurrence Handle9804376

    PubMed  Google Scholar 

  • L Schöls AM Vieira-Saecker S Schöls H Przuntek JT Epplen O Riess (1995) ArticleTitleTrinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients. Hum Mol Genet 4 1001–1005 Occurrence Handle7655453

    PubMed  Google Scholar 

  • L Schöls G Amoiridis T Büttner H Przuntek JT Epplen O Riess (1997a) ArticleTitleAutosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes? Ann Neurol 42 924–932 Occurrence Handle10.1002/ana.410420615

    Article  Google Scholar 

  • L Schöls S Gispert M Vorgerd AM Menezes Vieira-Saecker P Blanke G Auburger G Amoiridis S Meves JT Epplen H Przuntek SM Pulst O Riess (1997b) ArticleTitleSpinocerebellar ataxia type 2. Genotype and phenotype in German kindreds. Arch Neurol 54 1073–1080

    Google Scholar 

  • KG Smithson BA MacVicar GI Hatton (1983) ArticleTitlePolyethylene glycol embedding: a technique compatible with immunocytochemistry, enzyme histochemistry, histofluorescence and intracellular staining. Neurosci Methods 7 27–41 Occurrence Handle10.1016/0165-0270(83)90016-X

    Article  Google Scholar 

  • CC Verschuuren-Bemelmans ER Brunt M Burton RG Mensink MA van der Meulen NH Smit I Stolte-Dijkstra CH Buys H Scheffer (1995) ArticleTitleRefinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type I. Hum Genet 96 691–694 Occurrence Handle10.1007/BF00210301 Occurrence Handle8522329

    Article  PubMed  Google Scholar 

  • J Voogd M Glickstein (1998) ArticleTitleThe anatomy of the cerebellum. Trends Neurosci 21 370–375 Occurrence Handle10.1016/S0166-2236(98)01318-6 Occurrence Handle9735944

    Article  PubMed  Google Scholar 

  • Voogd J, Feirabend AKP, Schoen JHR (1990) Cerebellum and precerebellar nuclei. In: Paxinos G (ed) The human central nervous system. Academic Press, San Diego, pp 321–386

  • HY Zoghbi H Orr (2000) ArticleTitleGlutamine repeats and neurodegeneration. Ann Rev Neurosci 23 217–247 Occurrence Handle10.1146/annurev.neuro.23.1.217 Occurrence Handle10845064

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rüb, U., Gierga, K., Brunt, E. et al. Spinocerebellar ataxias types 2 and 3: degeneration of the precerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum. J Neural Transm 112, 1523–1545 (2005). https://doi.org/10.1007/s00702-005-0287-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00702-005-0287-3

Navigation