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The Journal of Biophysical and Biochemical Cytology logoLink to The Journal of Biophysical and Biochemical Cytology
. 1960 Jul 1;7(4):685–696. doi: 10.1083/jcb.7.4.685

Electron Microscopic Study of Demyelination in an Experimentally Induced Lesion in Adult Cat Spinal Cord

Richard P Bunge 1, Mary Bartlett Bunge 1, Hans Ris 1
PMCID: PMC2224890  PMID: 13805917

Abstract

Plaques of subpial demyelination were induced in adult cat spinal cords by repeated withdrawal and reinjection of cerebrospinal fluid. Peripheral cord was fixed by replacing cerebrospinal fluid available at cisternal puncture with 3 per cent buffered OsO4. Following extirpation, surface tissue was further fixed in 2 per cent buffered OsO4, dehydrated in ethanol, and embedded in araldite. Normal subpial cord consists mainly of myelinated axons and two types of macroglia, fibrous astrocytes and oligodendrocytes. Twenty-nine hours after lesion induction most myelin sheaths are deteriorating and typical macroglia are no longer visible. Phagocytosis of myelin debris has begun. In 3-day lesions, axons are intact and their mitochondria and neurofibrils appear normal despite continued myelin breakdown. All axons are completely demyelinated by 6 days. They lack investments only briefly, however, for at 10 and 14 days, macroglial processes appear and embrace them. These macroglia do not resemble either one of the normally occurring glia; their dense cytoplasm contains fibrils in addition to the usual organelles. It is proposed that these macroglia, which later accomplish remyelination, are the hypertrophic or swollen astrocytes of classical neuropathology. The suggestion that these astrocytes possess the potential to remyelinate axons in addition to their known ability to form cicatrix raises the possibility of pharmacological control of their expression.

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Selected References

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  1. ADAMS R. D., KUBIK C. S. The morbid anatomy of the demyelinative disease. Am J Med. 1952 May;12(5):510–546. doi: 10.1016/0002-9343(52)90234-9. [DOI] [PubMed] [Google Scholar]
  2. BUNGE R. P., SETTLAGE P. H. Neurological lesions in cats following cerebrospinal fluid manipulation. J Neuropathol Exp Neurol. 1957 Oct;16(4):471–491. doi: 10.1097/00005072-195710000-00003. [DOI] [PubMed] [Google Scholar]
  3. DE ROBERTIS E., GERSCHENFELD H. M., WALD F. Cellular mechanism of myelination in the central nervous system. J Biophys Biochem Cytol. 1958 Sep 25;4(5):651–656. doi: 10.1083/jcb.4.5.651. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. FARQUHAR M. G., HARTMANN J. F. Neuroglial structure and relationships as revealed by electron microscopy. J Neuropathol Exp Neurol. 1957 Jan;16(1):18–39. doi: 10.1097/00005072-195701000-00003. [DOI] [PubMed] [Google Scholar]
  5. GERSCHENFELD H. M., WALD F., ZADUNAISKY J. A., DE ROBERTIS E. D. Function of astroglia in the water-ion metabolism of the central nervous system: an electron microscope study. Neurology. 1959 Jun;9(6):412–425. doi: 10.1212/wnl.9.6.412. [DOI] [PubMed] [Google Scholar]
  6. GLAUERT A. M., GLAUERT R. H. Araldite as an embedding medium for electron microscopy. J Biophys Biochem Cytol. 1958 Mar 25;4(2):191–194. doi: 10.1083/jcb.4.2.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. GLAUERT A. M., GLAUERT R. H., ROGERS G. E. A new embedding medium for electron microscopy. Nature. 1956 Oct 13;178(4537):803–803. doi: 10.1038/178803a0. [DOI] [PubMed] [Google Scholar]
  8. GRAY E. G. Electron microscopy of neuroglial fibrils of the cerebral cortex. J Biophys Biochem Cytol. 1959 Aug;6(1):121–122. doi: 10.1083/jcb.6.1.121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. HELLER I. H., ELLIOTT K. A. The metabolism of normal brain and human gliomas in relation to cell type and density. Can J Biochem Physiol. 1955 May;33(3):395–403. [PubMed] [Google Scholar]
  10. KOENIG H. An autoradiographic study of nucleic acid and protein turnover in the mammalian neuraxis. J Biophys Biochem Cytol. 1958 Nov 25;4(6):785–792. doi: 10.1083/jcb.4.6.785. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. KOENIG H. Incorporation of adenine-8-C-14 and orotic-6-C-14 acid into nucleic acids of the feline neuraxis. Proc Soc Exp Biol Med. 1958 Feb;97(2):255–260. doi: 10.3181/00379727-97-23708. [DOI] [PubMed] [Google Scholar]
  12. KOREY S. R., ORCHEN M. Relative respiration of neuronal and glial cells. J Neurochem. 1959 Jan;3(3):277–285. doi: 10.1111/j.1471-4159.1959.tb12632.x. [DOI] [PubMed] [Google Scholar]
  13. LUMSDEN C. E. Demyelinating disease: the present situation. Proc R Soc Med. 1958 Sep;51(9):752–755. [PMC free article] [PubMed] [Google Scholar]
  14. LUSE S. A. Formation of myelin in the central nervous system of mice and rats, as studied with the electron microscope. J Biophys Biochem Cytol. 1956 Nov 25;2(6):777–784. doi: 10.1083/jcb.2.6.777. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. LUSE S. Ultrastructure of reactive and neoplastic astrocytes. Lab Invest. 1958 Jul-Aug;7(4):401–417. [PubMed] [Google Scholar]
  16. MATURANA H. R. The fine anatomy of the optic nerve of anurans--an electron microscope study. J Biophys Biochem Cytol. 1960 Feb;7:107–120. doi: 10.1083/jcb.7.1.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. PALAY S. L., PALADE G. E. The fine structure of neurons. J Biophys Biochem Cytol. 1955 Jan;1(1):69–88. doi: 10.1083/jcb.1.1.69. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. PEASE D. C., SCHULTZ R. L. Electron microscopy of rat cranial meninges. Am J Anat. 1958 Mar;102(2):301–321. doi: 10.1002/aja.1001020207. [DOI] [PubMed] [Google Scholar]
  19. SCHULTZ R. L., MAYNARD E. A., PEASE D. C. Electron microscopy of neurons and neuroglia of cerebral cortex and corpus callosum. Am J Anat. 1957 May;100(3):369–407. doi: 10.1002/aja.1001000305. [DOI] [PubMed] [Google Scholar]
  20. SCHULTZ R. L., PEASE D. C. Cicatrix formation in rat cerebral cortex as revealed by electron microscopy. Am J Pathol. 1959 Sep-Oct;35:1017–1041. [PMC free article] [PubMed] [Google Scholar]
  21. WATSON M. L. Staining of tissue sections for electron microscopy with heavy metals. II. Application of solutions containing lead and barium. J Biophys Biochem Cytol. 1958 Nov 25;4(6):727–730. doi: 10.1083/jcb.4.6.727. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. WATSON M. L. Staining of tissue sections for electron microscopy with heavy metals. J Biophys Biochem Cytol. 1958 Jul 25;4(4):475–478. doi: 10.1083/jcb.4.4.475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. ZIMMERMAN H. M., NETSKY M. G. The pathology of multiple sclerosis. Res Publ Assoc Res Nerv Ment Dis. 1950;28:271–312. [PubMed] [Google Scholar]

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