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Focal accumulation of phosphorylated neurofilaments within anterior horn cell in familial amyotrophic lateral sclerosis

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Summary

Distribution of phosphorylated neurofilament proteins within anterior horn cells in three cases of familial and six cases of sporadic amyotrophic lateral sclerosis (ALS) and ten control cases were investigated by using a monoclonal antibody. Two distinct staining patterns of perikarya were observed; (1) homogeneous pattern; either the entire or a part of the perikaryon was immunostained homogeneously (homogeneously diffuse or partial pattern); (2) focal pattern: perikarya contained very distinct, inclusion-like focal accumulation of immunoreactive products of various morphologies such as round, ring-shaped, cord-like, tube-like and more irregular shapes. The homogeneous pattern was found in all three groups but was most common in sporadic ALS. On the other hand, the focal pattern was seen almost exclusively in familial ALS. The focal accumulation of neurofilaments appears at least in part to be related to the Lewy body-like hyaline inclusion which is known to contain neurofilaments. In addition, cord-like swellings of neurites in familial ALS also showed focal neurofilament accumulation. These observations suggest that the focal accumulation of phosphorylated neurofilaments is characteristic of familial ALS, although it may not be specific to the entity. The pathological process(es) producing the neurofilamentous abnormality may play an important role in anterior horn cell degeneration in familial ALS.

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References

  1. Binder LI, Frankfurter A, Kebhun LI (1985) The distribution of tau in the mammalian central nervous system. J Cell Biol 101:1371–1378

    Google Scholar 

  2. Chou SM (1979) Pathognomy of intraneuronal inclusions in ALS. In: Tsubaki T, Toyokura Y (eds) Amyotrophic lateral sclerosis. University of Tokyo Press, Tokyo, pp 135–176

    Google Scholar 

  3. Chou SM (1987) Immunoreactivity of neurofilament epitopes in motor neurons of subacute ALS. J Neuropathol Exp Neurol 46:375

    Google Scholar 

  4. Chou SM (1988) Motorneuron inclusions in ALS are heavily ubiquitinated. J Neuropathol Exp Neurol 47:334

    Google Scholar 

  5. Gambetti P, Schecket G, Ghetti B, Hirano A, Dahl D (1983) Neurofibrillary changes in human brain. An immunocytochemical study with a neurofilament antiserum. J Neuropathol Exp Neurol 42:69–79

    Google Scholar 

  6. Goldman JE, Yen S-H (1986) Cytoskeletal protein abnormalities in neurodegenerative diseases. Ann Neurol 19:209–223

    Google Scholar 

  7. Greene C, Munoz-Garcia D, Perl DP, Pendlebury W (1986) Accumulation of phosphorylated neurofilaments in the anterior horn motor neurons of ALS patients. J Neuropathol Exp Neurol 45:332

    Google Scholar 

  8. Hershko A (1983) Ubiquitin: roles in protein modification and breakdown. Cell 34:11–12

    Google Scholar 

  9. Hirano A, Inoue K (1980) Early pathological changes of amyotrophic lateral sclerosis. Electron microscopic study of chromatolysis, spheroids and Bunina bodies. Neurol Med Chir (Tokyo) 13:148–160

    Google Scholar 

  10. Hirano A, Iwata M (1979) Pathology of motor neurons with special references to amyotrophic lateral sclerosis and related diseases. In: Tsubaki T, Toyokura Y (eds) Amyotrophic lateral sclerosis. University of Tokyo Press, Tokyo, pp 107–133

    Google Scholar 

  11. Hirano A, Kurland LT, Sayre GP (1967) Familial amyotrophic lateral sclerosis: a subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells. Arch Neurol 16:232–243

    Google Scholar 

  12. Hirano A, Donnenfeld H, Sasaki S, Nakano I (1984) Fine structural observations of neurofilamentous changes in amyotrophic lateral sclerosis. J Neuropathol Exp Neurol 43:461–470

    Google Scholar 

  13. Hirano A, Nakano I, Kurland LT, Mulder DW, Holley PW, Saccomanno G (1984) Fine structural study of neurofibrillary changes in a family with amyotrophic lateral sclerosis. J Neuropathol Exp Neurol 43:471–480

    Google Scholar 

  14. Hughes JT, Jerrome D (1971) Ultrastructure of anterior horn motor neurones in the Hirano-Kurland-Sayre type of combined neurological system degeneration. J Neurol Sci 13:389–399

    Google Scholar 

  15. Inoue K, Hirano A (1979) Early pathological changes of amyotrophic lateral sclerosis. Autopsy findings of a case of 10 months' duration. Neurol Med Chir (Tokyo) 11:448–455

    Google Scholar 

  16. Iwata M, Hirano A (1979) Current problems in the pathology of amyotrophic lateral sclerosis. Prog Neuropathol 4:277–298

    Google Scholar 

  17. Kato T, Hirano A, Kurland LT (1987) Asymmetric involvement of the spinal cord involving both large and small anterior horn cells in a case of familial amyotrophic lateral sclerosis. Clin Neuropathol 6:67–70

    Google Scholar 

  18. Kato T, Katagiri T, Hirano A, Sasaki H, Arai S (1988) Sporadic lower motor neuron disease with Lewy body-like inclusions: a new subgroup? Acta Neuropathol 76:208–211

    Google Scholar 

  19. Kondo A, Iwaki T, Tateishi J, Kishimoto K, Morimoto T, Oomura I (1986) Accumulation of neurofilaments in a sporadic case of amyotrophic lateral sclerosis. Jpn J Psychiatr Neurol 40:677–684

    Google Scholar 

  20. Ksiezak-Reding H, Dickson DW, Davies P, Yen S-H (1987) Recognition of tau epitopes by anti-neurofilament antibodies that bind to Alzheimer neurofibrillary tangles. Proc Natl Acad Sci USA 84:3410–3414

    Google Scholar 

  21. Kurisaki H, Ihara Y, Nukina N, Toyokura Y (1983) Immunocytochemical study of spinal cord using an antiserum to 200K peptides of neurofilament and antibodies to tubulin. Clin Neurol (Tokyo) 23:1013–1020

    Google Scholar 

  22. Kuroda S, Kuyama K, Morioka E, Ohtsuki S, Nanba R (1986) Sporadic amyotrophic lateral sclerosis with intracytoplasmic eosinophilic inclusions. A case closely akin to familial ALS. Neurol Med Chir (Tokyo) 24:31–37

    Google Scholar 

  23. Kusaka H, Imai T, Hashimoto S, Yamamoto T, Maya K, Yamasaki M (1988) Ultrastructural study of chromatolytic neurons in an adult-onset sporadic case of amyotrophic lateral sclerosis. Acta Neuropathol (Berl) 75:523–528

    Google Scholar 

  24. Kuzuhara S, Mori H, Izumiyama N, Yoshimura M, Ihara Y (1988) Lewy bodies are ubiquitinated. A light and electron microscopic immunocytochemical study. Acta Neuropathol (Berl) 75:345–353

    Google Scholar 

  25. Metcalf CW, Hirano A (1971) Amyotrophic lateral sclerosis: clinicopathological study of a family. Arch Neurol 24:518–523

    Google Scholar 

  26. Mizusawa H, Hirano A (1987) Lower motor neuron disease associated with a focal onion bulb formation in an anterior spinal root. Neurol Med Chir (Tokyo) 26:309–311

    Google Scholar 

  27. Munoz DG, Greene C, Perl DP, Selkoe DJ (1988) Accumulation of phosphorylated neurofilaments in anterior horn motoneurons of amyotrophic lateral sclerosis patients. J Neuropathol Exp Neurol 47:9–18

    Google Scholar 

  28. Nakano I, Hirano A, Kurland LT, Mulder DW, Holley PW, Saccomanno G (1984) Familial amyotrophic lateral sclerosis. Neuropathology of two brothers in American “C” family. Neurol Med Chir (Tokyo) 20:458–471

    Google Scholar 

  29. Nakazato Y, Sasaki A, Hirato J, Ishida Y (1984) Immunohistochemical localization of neurofilament protein in neuronal degenerations. Acta Neuropathol (Berl) 64:30–36

    Google Scholar 

  30. Powers JM, Horoupian DS, Schaumberg HH (1974) Wetherbee Ail. Documentation of a neurological disease in a Vermont family 90 years later. Can J Neurol Sci 1:139–140

    Google Scholar 

  31. Schlaepfer WW (1987) Neurofilaments: structure, metabolism and implications in diseases. J Neuropathol Exp Neurol 46:117–129

    Google Scholar 

  32. Schmidt ML, Carden MJ, Lee VM-Y, Trojanowski JQ (1987) Phosphate-dependent and-independent neurofilament epitopes in the axonal swellings of patients with motor neuron disease and controls. Lab Invest 56:282–294

    Google Scholar 

  33. Schochet SS, Hardman JM, Ladewig PP, Earle KM (1969) Intraneuronal conglomerate in sporadic motor neuron disease. A light and electron microscopic study. Arch Neurol 20:548–553

    Google Scholar 

  34. Sternberger LA, Sternberger NH (1983) Monoclonal antibodies distinguish phosphorylated and nonphosphorylated forms of neurofilaments in situ. Proc Natl Acad Sci USA 80:6126–6130

    Google Scholar 

  35. Takahashi K, Nakamura H, Okada E (1972) Heredetary amyotrophic lateral sclerosis. Histochemical and electron microscopic study of hyaline inclusions in motor neurons. Arch Neurol 27:292–299

    Google Scholar 

  36. Toyoshima I, Yamamoto A, Masamune O, Satare M (1989) Phosphorylation of neurofilament proteins and localization of axonal swelling in motor neuron disease. J Neurol Sci 89:269–278

    Google Scholar 

  37. Yen S-H, Crowe A, Dickson DW (1985) Monoclonal antibodies to Alzheimer neurofibrillary tangles. 1. Identification of polypeptides. Am J Pathol 120:282–291

    Google Scholar 

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Mizusawa, H., Matsumoto, S., Yen, S.H. et al. Focal accumulation of phosphorylated neurofilaments within anterior horn cell in familial amyotrophic lateral sclerosis. Acta Neuropathol 79, 37–43 (1989). https://doi.org/10.1007/BF00308955

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  • DOI: https://doi.org/10.1007/BF00308955

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