Abstract
Oligodendrocytes isolated from 4–6-week-old rat brains were transplanted into newborn shiverer brains. Cells were identified as mature oligodendrocytes both by immunocytological and ultrastructural criteria. Normal myelin was detected using immunolocalisation (with an anti-MBP antiserum) and electron microscopy (presence of the major dense line). Patches of normal myelin (made by transplanted oligodendrocytes), widely spread throughout the host brains, were detected between 20 and 130 days after grafting. No sign of acute rejection was observed, but the graft became progressively delimited by astrocytic processes forming a continuous basal lamina.
Keywords: Myelination, Matured oligodendrocytes, Shiverer transplantation model
References
- Aranella L.S., Robert M.S., Herndon M. Mature oligodendrocytes. Division following experimental demyelination in adult animalsArch. Neurol. 1984;41:1162–1165. doi: 10.1001/archneur.1984.04050220060015. [DOI] [PubMed] [Google Scholar]
- Baulac M., Lachapelle F., Gout O., Berger B., Baumann N., Gumpel M. Transplantations of oligodendrocytes in the new-born mouse brain. Extention of myelination by transplanted cells. Anatomical studyBrain Res. 1987;420:39–47. doi: 10.1016/0006-8993(87)90237-x. [DOI] [PubMed] [Google Scholar]
- Blakemore W.F. Observations on myelination and remyelination in the central nervous system. In: Garrod D.R., Feldman J.D., editors. Vol. 5. Cambridge University Press; London: 1981. pp. 289–308. (Development in the nervous system. British Society for Developmental Biology, Symposium). [Google Scholar]
- Blakemore W.F. Remyelination of demyelinated spinal cord axons by Schwann cells. In: Kao C.C., Bunge R.P., Reier P.J., editors. Spinal Cord Reconstruction. Raven Press; New York: 1983. pp. 281–291. [Google Scholar]
- Dal Canto M.C., Rabinowitz S.G. Experimental models of virus-induced demyelination of the central nervous system. Ann. Neurol. 1982;11:109–127. doi: 10.1002/ana.410110202. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eisenbarth G.S., Walsh F.S., Niremberg M. Vol. 76. 1979. Monoclonal antibody to a plasma membrane antigen of neurons; pp. 4913–4917. (Proc. Natl. Acad. Sci. USA). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Feigin I., Popoff N. Regeneration of myelin in multiple sclerosis: the role of mesenchymal cells in such regeneration and in myelin formation in the peripheral nervous system. Ann. Neurol. 1966;16:364–372. doi: 10.1212/wnl.16.4.364. [DOI] [PubMed] [Google Scholar]
- Folch-Pi J. Composition of the brain in relation to maturation. In: Waelch H., editor. Biochemistry of the Developing Nervous System. Academic Press; New York: 1955. pp. 121–136. [Google Scholar]
- Ffrench-Constant C., Raff M.C. Proliferating bipotential glial progenitor cells in adult rat optic nerve. Nature. 1986;319:499–502. doi: 10.1038/319499a0. [DOI] [PubMed] [Google Scholar]
- Gansmüller A., Lachapelle F., Baron-Van Evercooren A., Hauw J.J., Baumann N., Gumpel M. Transplantations of new-born CNS fragments into the brain of shiverer mutant mice: extensive myelination by transplanted oligodendrocytes. II. Electron microscopic study. Dev. Neurosci. 1986;8:197–207. doi: 10.1159/000112253. [DOI] [PubMed] [Google Scholar]
- Ghatak H., Hirano A., Donon Y., Zimmerman H.M. The myelination in MS with peripheral type myelin. Arch. Neurol. 1973;29:262–267. doi: 10.1001/archneur.1973.00490280074011. [DOI] [PubMed] [Google Scholar]
- Gumpel M., Lachapelle F., Jacque C., Baumann N. Central nervous tissue transplantation into mouse brain: differentiation of myelin from transplanted oligodendrocytes. In: Björklund A., Stenevi U., editors. Vol. 5. Elsevier; Amsterdam: 1985. pp. 151–158. (Neural Grafting in the Mammalian CNS, Fernström Symposium). [Google Scholar]
- Gumpel M., Lachapelle F., Gansmüller A., Baulac M., Baron-Van Evercooren A., Baumann N. Transplantations of human embryonic oligodendrocytes into shiverer brain. Ann. N. Y. Acad. Sci. 1987;495:71–85. doi: 10.1111/j.1749-6632.1987.tb23666.x. [DOI] [PubMed] [Google Scholar]
- Hall S.M. The effect of injections of lysophosphatidyl choline into white matter of the adult mouse spinal cord. J. Cell. Sci. 1972;10:535–546. doi: 10.1242/jcs.10.2.535. [DOI] [PubMed] [Google Scholar]
- Harrison B.M. Remyelination in the central nervous system. In: Hallpike J.F., Adams C.W., Tourtelotte W.W., editors. Multiple Sclerosis. University Press; 1983. pp. 461–478. [Google Scholar]
- Herndon R.M., Price D.L., Weiner L.P. Regeneration of oligodendroglia during recovery from demyelinating disease. Science. 1977;195:693. doi: 10.1126/science.190678. [DOI] [PubMed] [Google Scholar]
- Jacque C., Privat A., Dupouey P., Bourre J.M., Bird T., Baumann N. Vol. 1. 1978. Shiverer mouse: a dysmyelinating mutant with absence of major dense line and basic protein in myelin; p. 131. (Proc. Eur. Soc. Neurochem.). [Google Scholar]
- Lachapelle F., Gumpel M., Baulac M., Jacque C., Duc P., Baumann N. Transplantation of CNS fragments into the brain of shiverer mutant mice: extensive myelination by implanted oligodendrocytes. I. Immunohistochemical studies. Dev. Neurosci. 1983/1984;6:325–334. doi: 10.1159/000112359. [DOI] [PubMed] [Google Scholar]
- Lisak R.P., Pleasure D.W., Silberberg D.H., Manning M.C., Saida T. Long term culture of oligodendroglia isolated with a Percoll gradient. Brain Res. 1981;223:107–122. doi: 10.1016/0006-8993(81)90809-x. [DOI] [PubMed] [Google Scholar]
- Lubetzki C., Lombrail P., Hauw J.J., Zalc B. Multiple sclerosis: rat and human oligodendrocytes are not the target for cerebrospinal fluid immunoglobulins. Neurology. 1986;36:524–528. doi: 10.1212/wnl.36.4.524. [DOI] [PubMed] [Google Scholar]
- Ludwin S.K. Central nervous system demyelination and remyelination in the mouse. An ultrastructural study of cuprizone toxicityLab. Invest. 1978;39:597–612. [PubMed] [Google Scholar]
- Ludwin S.K. Proliferation of mature oligodendrocytes after trauma to the central nervous system. Nature. 1984;308:274–275. doi: 10.1038/308274a0. [DOI] [PubMed] [Google Scholar]
- Monge M., Kadiiski D., Jacque C., Zalc B. Oligodendroglial expression and deposition of four major myelin constituents in the myelin sheath during development. An in vivo studyDev. Neurosci. 1986;8:222–235. doi: 10.1159/000112255. [DOI] [PubMed] [Google Scholar]
- Mori S., Leblond C.P. Electron microscopic identification of three classes of oligodendrocytes and a preliminary study of their proliferative activity in the corpus callosum of young rats. J. Comp. Neurol. 1970;139:1–30. doi: 10.1002/cne.901390102. [DOI] [PubMed] [Google Scholar]
- Nagashima K., Wege H., Meyermann R., Ter Meulen V. Demyelinating encephalomyelitis induced by long term corona-virus infection in rats. Acta Neuropathol. 1979;45:205–213. doi: 10.1007/BF00702672. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Perier O., Gregoire A. Electron microscopic features of multiple sclerosis lesions. Brain. 1965;88:937–952. doi: 10.1093/brain/88.5.937. [DOI] [PubMed] [Google Scholar]
- Prineas J.W., Connel F. Remyelination in multiple sclerosis. Ann. Neurol. 1979;5:22–31. doi: 10.1002/ana.410050105. [DOI] [PubMed] [Google Scholar]
- Privat A., Jacque C., Bourre J.M., Dupouey P., Baumann N. Absence of the major dense line in the mutant mouse shiverer. Neurosci. Lett. 1979;12:107–112. doi: 10.1016/0304-3940(79)91489-7. [DOI] [PubMed] [Google Scholar]
- Raff M.C., Fields K.L., Hakomori S.I., Mirsky R., Pruss R.M., Winter J. Cell types specific markers for distinguishing and studying neurons and the major classes of glial cells in culture. Brain Res. 1979;174:283–308. doi: 10.1016/0006-8993(79)90851-5. [DOI] [PubMed] [Google Scholar]
- Raff M.C., Abney E.R., Cohen J., Lindsay R., Noble M. Two types of astrocytes in cultures of developing rat white matter: differences in morphology, surface gangliosides, and growth characteristics. J. Neurosci. 1983;3(6):1289–1300. doi: 10.1523/JNEUROSCI.03-06-01289.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Raff M.C., Abney E.R., Fok-Seang J. Reconstitution of a developmental clock in vitro: A critical role for astrocytes in the timing of oligodendrocyte differentiation. Cell. 1985;42:61–69. doi: 10.1016/s0092-8674(85)80101-x. [DOI] [PubMed] [Google Scholar]
- Roach A., Takahashi N., Pravtcheva D., Ruddle F., Hood L. Chromosomal mapping of mouse myelin basic protein gene and structure and transcription of the partially deleted gene in shiverer mutant mice. Cell. 1985;42:149–155. doi: 10.1016/s0092-8674(85)80110-0. [DOI] [PubMed] [Google Scholar]
- Sidman R.L., Conover C.S., Carson J.H. Shiverer gene maps near the distal end of chromosome 18 in the mouse. Cell Genet. 1985;39:241–245. doi: 10.1159/000132151. [DOI] [PubMed] [Google Scholar]
- Small R.K., Riddle P., Noble M. Evidence for migration of oligodendrocyte-type-2 astrocyte progenitor cells into the developing rat optic nerve. Nature. 1987;328:155–157. doi: 10.1038/328155a0. [DOI] [PubMed] [Google Scholar]
- Sternberger L.A., Hardy P.H., Cuculus J.J., Meyer H.G. The unlabelled antibody enzyme method of immunochemistry. Preparation and properties of soluble antigen-antibody complex (horseradish peroxydase and anti horse-radish peroxydase) and its use in identification of spirochetesJ. Histochem. 1970;18:315–333. doi: 10.1177/18.5.315. [DOI] [PubMed] [Google Scholar]
- Szuchet S., Polak P.E., Yim S.H. Mature oligodendrocytes cultured in the absence of neurons recapitulate the ontogenic development of myelin membranes. Dev. Neurosci. 1986;8:208–221. doi: 10.1159/000112254. [DOI] [PubMed] [Google Scholar]
- Weiner L.P., Waxman S.G., Stohlman A., Kwan A. Remyelination following viral induced demyelination. Ferric ion-ferrocyanide staining of nodes of Ranvier within the CNSAnn. Neurol. 1980;8:580–583. doi: 10.1002/ana.410080606. [DOI] [PubMed] [Google Scholar]
- Wood P.M., Bunge R. Myelination of cultured dorsal root ganglion neurons by oligodendrocytes obtained from adult rat. J. Neurol. Sci. 1986;74:153–169. doi: 10.1016/0022-510x(86)90101-2. [DOI] [PubMed] [Google Scholar]
- Yavin E., Yavin Z. Attachment and culture of dissociated cells from rat embryo cerebral hemispheres on Polylysine coated surface. J. Cell. Biol. 1974;62:540–546. doi: 10.1083/jcb.62.2.540. [DOI] [PMC free article] [PubMed] [Google Scholar]