Skip to main content
Log in

Spinal cord multiple sclerosis lesions in Japanese patients: Schwann cell remyelination occurs in areas that lack glial fibrillary acidic protein (GFAP)

  • Original Works
  • Published:
Acta Neuropathologica Aims and scope Submit manuscript

Summary

To extend earlier observations on Schwann cell remyelination in multiple sclerosis (MS) lesions (Itoyama et al. 1983) we immunostained spinal cord sections from eight Japanese MS patients with antiserum to Po glycoprotein, a major constituent of peripheral nervous system (PNS) myelin, myelin basic protein (MBP), and glial fibrillary acidic protein (GFAP). Spinal cord sections from six of the eight Japanese MS patients contained large clusters of peripheral myelin sheaths with anti-Po immunoreactivity. In lesions found in four of the six patients, thousands of Po-stained PNS myelin sheaths were present. Necrosis was prominent in these lesions which included more than half of the spinal cord's transverse area. The number and density of regenerating myelin sheaths of peripheral origin were much greater than we observed in MS spinal cord lesions of white people (Itoyama et al. 1983). Anti-GFAP immunoreactivity was present in most brain and spinal cord lesions. However, the areas in lesions that contained large groups of PNS myelin sheaths lacked anti-GFAP immunoreactivity. Our data suggest that spinal MS lesions that are large, severely demyelinated, and partially necrotic may contain factors that inhibit fibrous astrogliosis. These factors, other substances in the large lesions and/or the lack of astrocytic scarring could then promote Schwann cell invasion, multiplication, and remyelination of surviving axons.

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.

Institutional subscriptions

Similar content being viewed by others

References

  • Adelman LS, Aronson SM (1972) Intramedullary nerve fiber and Schwann cell proliferation within the spinal cord (schwannosis). Neurology (Minneap) 22:726–731

    Google Scholar 

  • Bignami A, Eng LF, Dahl D, Uyeda CT (1972) Localization of the glial fibrillary acidic protein in astrocytes by immunofluorescence. Brain Res 43:429–435

    Google Scholar 

  • Bignami A, Dahl D (1974) Astrocyte-specific protein and neuroglial differentiation. An immunofluorescence study with antibodies to the glial fibrillary acidic protein. J Comp Neurol 153:27–38

    Google Scholar 

  • Blakemore WF, Patterson RC (1975) Observations on the interactions of Schwann cells and astrocytes following X-irradiation of neonatal rat spinal cord. J Neurocytol 4:573–585

    Google Scholar 

  • Blakemore WF (1976) Invasion of Schwann cells into the spinal cord of the rat following local injections of lysolecithin. Neuropathol App Neurobiol 2:21–39

    Google Scholar 

  • Eng LF, Vanderhaeghen JJ, Bignami A, Gerstl B (1971) An acidic protein isolated from fibrous astrocytes. Brain Res 28:351–354

    Google Scholar 

  • Everly JL, Brady RO, Quarles RH (1973) Evidence that the major protein in rat sciatic nerve myelin is a glycoprotein. J Neurochem 21:329–344

    Google Scholar 

  • Feigin I, Popoff N (1966) Regeneration of myelin in multiple sclerosis: the role of mesenchymal cells in such regeneration and in myelin formation in the peripheral nervous system. Neurology (Minneap) 16:364–372

    Google Scholar 

  • Feigin I, Ogata J (1971) Schwann cells and peripheral myelin within human central nervous tissues: the mesenchymal character of Schwann cells. J Neuropathol Exp Neurol 30:603–612

    Google Scholar 

  • Ghatak NR, Hirano A Doron Y, Zimmerman HM (1973) Remyelination in multiple sclerosis with peripheral type myelin. Arch Neurol 29:262–267

    Google Scholar 

  • Harrison BM, McDonald WI, Ochoa J (1972) Remyelination in the central diphtheria toxin lesion. J Neurol Sci 16:293–302

    Google Scholar 

  • Hirano A, Zimmerman HM, Levine S (1969) Electron-microscopic observations of peripheral myelin in a central nervous system lesion. Acta Neuropathol (Berl) 12:348–365

    Google Scholar 

  • Ikuta F, Koga M, Takeda S, Ohama E, Takeshita I, Ogawa H, Wang M (1982) Comparison of MS pathology between 70 American and 75 Japanese autopsy cases. In: Kuroiwa Y, Kurland LT (eds) Multiple sclerosis, East and West. Kyushu University Press, Fukuoka, pp 297–306

    Google Scholar 

  • Itoyama Y, Sternberger NH, Kies MW, Cohen SR, Richardson EP, Jr, Webster H deF (1980a) Immunocytochemical method to identify myelin basic protein in oligodendroglia and myelin sheaths of the human nervous system. Ann Neurol 7:157–166

    Google Scholar 

  • Itoyama Y, Sternberger NH, Webster H deF, Quarles RH, Cohen SR, Richardson EP, Jr (1980b) Immunocytochemical observation on the distribution of myelin-associated glycoprotein and myelin basic protein in multiple sclerosis lesions. Ann Neurol 7:167–177

    Google Scholar 

  • Itovama Y, Webster H deF, Richardson EP, Jr, Trapp BD (1983) Schwann cell remyelination of demyelinated axons in spinal cord multiple sclerosis. Ann Neurol 14:339–346

    Google Scholar 

  • Itoyama Y, Ohnishi A, Tateishi J Kuroiwa Y, Webster H deF (1984) Immunocytochemical study of Schwann cell remyelination in spinal cord lesions of Japanese multiple sclerosis patients. In: Sobue I (ed) Peripheral neuropathy. Proceedings of the International Symposium on Peripheral Neuropathy, Excerpta Medica, Tokyo (in press)

    Google Scholar 

  • Kuroiwa Y, Igata A, Itahara K, Koshijima S, Tsubaki T, Toyokura Y, Shibasaki H (1975) Nationwide survey of multiple sclerosis in Japan. Clinical analysis of 1,084 cases. Neurology (Minneap) 25:845–851

    Google Scholar 

  • Lassmann H, Kitz K, Wisniewski HM (1980) Structural variability of demyelinating lesions in different models of subacute and chronic experimental allergic encephalomyelitis. Acta Neuropathol (Berl) 51:191–201

    Google Scholar 

  • Newcombe J, Cuzner ML, Roytta M, Frey H (1980) White matter proteins in multiple sclerosis. J Neurochem 34:700–708

    Google Scholar 

  • Ogata J, Feigin I (1975) Schwann cell and regenerated peripheral myelin in multiple sclerosis: an ultrastructural study. Neurology (Minneap) 25:713–716

    Google Scholar 

  • Prineas JW, Connell F (1979) Remyelination in multiple sclerosis. Ann Neurol 5:22–31

    Google Scholar 

  • Raine CS (1976) On the occurrence of Schwann cells within the normal central nervous system. J Neurocytol 5:371–380

    Google Scholar 

  • Raine CS, Traugott U, Stone SH (1978) Glial bridges and Schwann cells migration during chronic demyelination in the CNS. J Neurocytol 7:541–553

    Google Scholar 

  • Reier PJ, Webster H deF (1974) Regeneration and remyelination of Xenopus tadpole optic nerve fibers following transection or erush. J Neurocytol 3:591–618

    Google Scholar 

  • Schober R, Itoyama Y, Sternberger NH, Trapp BD, Richardson EP, Jr, Asbury AK, Quarles RH, Webster H deF (1981) Immunocytochemical study of Po glycoprotein, P1 and P2 basic protein, and myelin-associated glycoprotein (MAG) in lesions of idiopathic polyneuritis. Neuropathol Appl Neurobiol 7:421–434

    Google Scholar 

  • Shibasaki H, McDonald WI, Kuroiwa Y (1981) Racial modification of clinical picture of multiple sclerosis: Comparison between British and Japanese patients. J Neurol Sci 49:253–271

    Google Scholar 

  • Shiraki H (1968) The comparative study of rabies postvaccinal encephalomyelitis and demyelinating encephalomyelitides of unknown origin, with special reference to the Japanese cases. In: Bailey OT, Smith DE (eds) The central nervous system some experimental models of neurological diseases. Williams and Wilkins, Baltimore, pp 87–123

    Google Scholar 

  • Snyder, DH, Valsamis MP, Stone SH, Raine CS (1975) Progressive and reparatory events in chronic experimental allegic encephalomyelitis. J Neuropathol Exp Neurol 34:209–221

    Google Scholar 

  • Sternberger LA, Hardy Ph, Jr, Cuculis JJ, Meyer HG (1970) The unlabeled antibody enzyme method of immunocytochemistry: preparation and properties of soluble antigen-antibody complex (horseradish peroxidase-antihorseradish peroxidase) and its use in identification of spirochetes. J Histochem Cytochem 18:315–333

    Google Scholar 

  • Sternberger LA, Hardy PH, Jr, Cuculis JJ, Meyer HG (1970) The The unlabeled antibody enzyme method of immunomyelin-forming oligodendrocytes of newborn rat CNS. J Neurocytol 7:251–263

    Google Scholar 

  • Sternberger NH, Itoyama Y, Kies MW, Webster H deF (1978b) Myelin basic protein demonstrated immunocytochemically in oligodendroglia prior to myelin sheath formation. Proc Natl Acad Sci USA 75:2521–2524

    Google Scholar 

  • Trapp BD, McIntyre LJ, Quarles RH, Sternberger NH, Webster H deF (1979) Immunocytochemical localization of rat peripheral nervous system myelin proteins: P2 protein is not a component of all peripheral nervous system myelin sheaths. Proc Natl Acad Sci USA 76:3552–3556

    Google Scholar 

  • Trapp BD, Itoyama Y, Sternberger NH, Quarles RH, Webster H deF (1981) Immunocytochemical localization of P0 protein in Golgi complex membranes and myelin of developing rat Schwann cells. J Cell Biol 90:1–6

    Google Scholar 

  • Webster H deF, Trapp BD, Sternberger NH (1981) Myelinforming glial cells: morphological and immunocytochemical observations. In: Garrod DR (ed) Development in the nervous system. Cambridge University Press, Cambridge, pp 265–288

    Google Scholar 

  • Wood JG, Dawson RMC (1973) A major myelin glycoprotein of sciatic nerve. J Neurochem 21:717–719

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Itoyama, Y., Ohnishi, A., Tateishi, J. et al. Spinal cord multiple sclerosis lesions in Japanese patients: Schwann cell remyelination occurs in areas that lack glial fibrillary acidic protein (GFAP). Acta Neuropathol 65, 217–223 (1985). https://doi.org/10.1007/BF00687001

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00687001

Key words

Navigation