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. 1971 Feb 1;48(2):348–367. doi: 10.1083/jcb.48.2.348

THE GEOMETRY OF PERIPHERAL MYELIN SHEATHS DURING THEIR FORMATION AND GROWTH IN RAT SCIATIC NERVES

Henry deF Webster 1
PMCID: PMC2108190  PMID: 4928020

Abstract

In rat sciatic nerves, a small bundle of fibers was identified in which myelin sheaths were absent at birth, appeared within 3 days, and grew rapidly for 2 wk. During this interval, nerves were removed from littermates and were sectioned serially in the transverse plane. Alternating sets of thin and thick sections were used to prepare electron micrograph montages in which single myelinating axons could be identified and traced distally. During the formation of the first spiral turn, the mesaxon's length and configuration varied when it was studied at different levels in the same Schwann cell. The position of the mesaxon's termination shifted while its origin, at the Schwann cell surface, remained relatively constant. Along myelin internodes composed of two to six spiral turns, there were many variations in the number of lamellae and their contour. Near the mesaxon's origin, longitudinal strips of cytoplasm separated the myelin layers. Thicker sheaths were larger in circumference, more circular in transverse sections, and more uniform at different levels. Irregularities were confined to the paranodal region, and separation of lamellae by cytoplasm occurred at Schmidt-Lantermann clefts. Approximate dimensions of the bundle, its largest fibers, and their myelin sheaths were measured and calculated. The myelin membrane's transverse length and area increased exponentially with time; the growth rate increased rapidly during the formation of the first four to six spiral layers and remained relatively constant during the subsequent enlargement of the compact sheath.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Allt G. Ultrastructural features of the immature peripheral nerve. J Anat. 1969 Sep;105(Pt 2):283–293. [PMC free article] [PubMed] [Google Scholar]
  2. BEN GEREN B. The formation from the Schwann cell surface of myelin in the peripheral nerves of chick embryos. Exp Cell Res. 1954 Nov;7(2):558–562. doi: 10.1016/s0014-4827(54)80098-x. [DOI] [PubMed] [Google Scholar]
  3. Bunge R. P. Glial cells and the central myelin sheath. Physiol Rev. 1968 Jan;48(1):197–251. doi: 10.1152/physrev.1968.48.1.197. [DOI] [PubMed] [Google Scholar]
  4. Caston J. D., Singer M. Amino acid uptake and incorporation into macromolecules of peripheral nerves. J Neurochem. 1969 Sep;16(9):1309–1318. doi: 10.1111/j.1471-4159.1969.tb05981.x. [DOI] [PubMed] [Google Scholar]
  5. Friede R. L., Samorajski T. Myelin formation in the sciatic nerve of the rat. A quantitative electron microscopic, histochemical and radioautographic study. J Neuropathol Exp Neurol. 1968 Oct;27(4):546–570. [PubMed] [Google Scholar]
  6. Friede R. L., Samorajski T. Relation between the number of myelin lamellae and axon circumference in fibers of vagus and sciatic nerves of mice. J Comp Neurol. 1967 Jul;130(3):223–231. doi: 10.1002/cne.901300304. [DOI] [PubMed] [Google Scholar]
  7. Friede R. L., Samorajski T. The clefts of Schmidt-Lantermann: a quantitative electron microscopic study of their structure in developing and adult sciatic nerves of the rat. Anat Rec. 1969 Sep;165(1):89–101. doi: 10.1002/ar.1091650110. [DOI] [PubMed] [Google Scholar]
  8. Hedley-Whyte E. T., Rawlins F. A., Salpeter M. M., Uzman B. G. Distribution of cholesterol-1,2-H3 during maturation of mouse peripheral nerve. Lab Invest. 1969 Dec;21(6):536–547. [PubMed] [Google Scholar]
  9. Hendelman W. J., Bunge R. P. Radioautographic studies of choline incorporation into peripheral nerve myelin. J Cell Biol. 1969 Jan;40(1):190–208. doi: 10.1083/jcb.40.1.190. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Horrocks L. A. Composition of mouse brain myelin during development. J Neurochem. 1968 Jun;15(6):483–488. doi: 10.1111/j.1471-4159.1968.tb08945.x. [DOI] [PubMed] [Google Scholar]
  11. LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Matthews M. A. An electron microscopic study of the relationship between axon diameter and the initiation of myelin production in the peripheral nervous system. Anat Rec. 1968 Jul;161(3):337–351. doi: 10.1002/ar.1091610306. [DOI] [PubMed] [Google Scholar]
  13. Naitoh Y. Ionic control of the reversal response of cilia in Paramecium caudatum. A calcium hypothesis. J Gen Physiol. 1968 Jan;51(1):85–103. doi: 10.1085/jgp.51.1.85. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Napolitano L. M., Scallen T. J. Observations on the fine structure of peripheral nerve myelin. Anat Rec. 1969 Jan;163(1):1–6. doi: 10.1002/ar.1091630101. [DOI] [PubMed] [Google Scholar]
  15. PETERS A., MUIR A. R. The relationship between axons and Schwann cells during development of peripheral nerves in the rat. Q J Exp Physiol Cogn Med Sci. 1959 Jan;44(1):117–130. doi: 10.1113/expphysiol.1959.sp001366. [DOI] [PubMed] [Google Scholar]
  16. ROBERTSON J. D. New observations on the ultrastructure of the membranes of frog peripheral nerve fibers. J Biophys Biochem Cytol. 1957 Nov 25;3(6):1043–1048. doi: 10.1083/jcb.3.6.1043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. ROBERTSON J. D. The qnit membrane of cells and mechanisms of myelin formation. Res Publ Assoc Res Nerv Ment Dis. 1962;40:94–158. [PubMed] [Google Scholar]
  18. ROBERTSON J. D. The ultrastructure of Schmidt-Lanterman clefts and related shearing defects of the myelin sheath. J Biophys Biochem Cytol. 1958 Jan 25;4(1):39–46. doi: 10.1083/jcb.4.1.39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. ROBERTSON J. D. The ultrastructure of adult vertebrate peripheral myelinated nerve fibers in relation to myelinogenesis. J Biophys Biochem Cytol. 1955 Jul 25;1(4):271–278. doi: 10.1083/jcb.1.4.271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Revel J. P., Hamilton D. W. The double nature of the intermediate dense line in peripheral nerve myelin. Anat Rec. 1969 Jan;163(1):7–15. doi: 10.1002/ar.1091630102. [DOI] [PubMed] [Google Scholar]
  21. Rosenbluth J. Redundant myelin sheaths and other ultrastructural features of the toad cerebellum. J Cell Biol. 1966 Jan;28(1):73–93. doi: 10.1083/jcb.28.1.73. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Smith M. E. The turnover of myelin in the adult rat. Biochim Biophys Acta. 1968 Oct 22;164(2):285–293. doi: 10.1016/0005-2760(68)90154-9. [DOI] [PubMed] [Google Scholar]
  23. VENABLE J. H., COGGESHALL R. A SIMPLIFIED LEAD CITRATE STAIN FOR USE IN ELECTRON MICROSCOPY. J Cell Biol. 1965 May;25:407–408. doi: 10.1083/jcb.25.2.407. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. WEBSTER H. D., SPIRO D. Phase and electron microscopic studies of experimental demyelination. I. Variations in myelin sheath contour in normal guinea pig sciatic nerve. J Neuropathol Exp Neurol. 1960 Jan;19:42–69. [PubMed] [Google Scholar]

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