Abstract
In view of reports that the nerve fibers of the sea prawn conduct impulses more rapidly than other invertebrate nerves and look like myelinated vertebrate nerves in the light microscope, prawn nerve fibers were studied with the electron microscope. Their sheaths are found to have a consistent and unique structure that is unlike vertebrate myelin in four respects: (1) The sheath is composed of 10 to 50 thin (200- to 1000-A) layers or laminae; each lamina is a cellular process that contains cytoplasm and wraps concentrically around the axon. The laminae do not connect to form a spiral; in fact, no cytoplasmic continuity has been demonstrated among them. (2) Nuclei of sheath cells occur only in the innermost lamina of the sheath; thus, they lie between the sheath and the axon rather than outside the sheath as in vertebrate myelinated fibers. (3) In regions in which the structural integrity of the sheath is most prominent, radially oriented stacks of desmosomes are formed between adjacent laminae. (4) An ∼200-A extracellular gap occurs around the axon and between the innermost sheath laminae, but it is separated from surrounding extracellular spaces by gap closure between the outer sheath laminae, as the membranes of adjacent laminae adhere to form external compound membranes (ECM's). Sheaths are interrupted periodically to form nodes, analogous to vertebrate nodes of Ranvier, where a new type of glial cell called the "nodal cell" loosely enmeshes the axon and intermittently forms tight junctions (ECM's) with it. This nodal cell, in turn, forms tight junctions with other glial cells which ramify widely within the cord, suggesting the possibility of functional axon-glia interaction.
Full Text
The Full Text of this article is available as a PDF (2.9 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BUNGE M. B., BUNGE R. P., RIS H. Ultrastructural study of remyelination in an experimental lesion in adult cat spinal cord. J Biophys Biochem Cytol. 1961 May;10:67–94. doi: 10.1083/jcb.10.1.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DEWEY M. M., BARR L. A STUDY OF THE STRUCTURE AND DISTRIBUTION OF THE NEXUS. J Cell Biol. 1964 Dec;23:553–585. doi: 10.1083/jcb.23.3.553. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HAMA K. Some observations on the fine structure of the giant nerve fibers of the earthworm, Eisenia foetida. J Biophys Biochem Cytol. 1959 Aug;6(1):61–66. doi: 10.1083/jcb.6.1.61. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Huxley A. F., Stämpfli R. Evidence for saltatory conduction in peripheral myelinated nerve fibres. J Physiol. 1949 May 15;108(3):315–339. [PMC free article] [PubMed] [Google Scholar]
- 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]
- McALEAR J. H., MILBURN N. S., CHAPMAN G. B. The fine structure of Schwann cells, nodes of Ranvier and Schmidt-Lanterman incisures in the central nervous system of the crab, Cancer irroratus. J Ultrastruct Res. 1958 Dec;2(2):171–176. doi: 10.1016/s0022-5320(58)90015-7. [DOI] [PubMed] [Google Scholar]
- PETERS A. The formation and structure of myelin sheaths in the central nervous system. J Biophys Biochem Cytol. 1960 Oct;8:431–446. doi: 10.1083/jcb.8.2.431. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROBERTSON J. D., BODENHEIMER T. S., STAGE D. E. THE ULTRASTRUCTURE OF MAUTHNER CELL SYNAPSES AND NODES IN GOLDFISH BRAINS. J Cell Biol. 1963 Oct;19:159–199. doi: 10.1083/jcb.19.1.159. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- ROBERTSON J. D. Structural alterations in nerve fibers produced by hypotonic and hypertonic solutions. J Biophys Biochem Cytol. 1958 Jul 25;4(4):349–364. doi: 10.1083/jcb.4.4.349. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROSENBLUTH J., PALAY S. L. The fine structure of nerve cell bodies and their myelin sheaths in the eighth nerve ganglion of the goldfish. J Biophys Biochem Cytol. 1961 Apr;9:853–877. doi: 10.1083/jcb.9.4.853. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROSENBLUTH J. The fine structure of acoustic ganglia in the rat. J Cell Biol. 1962 Feb;12:329–359. doi: 10.1083/jcb.12.2.329. [DOI] [PMC free article] [PubMed] [Google Scholar]
- UZMAN B. G., VILLEGAS G. M. A comparison of nodes of Ranvier in sciatic nerves with node-like structures in optic nerves of the mouse. J Biophys Biochem Cytol. 1960 Jul;7:761–762. doi: 10.1083/jcb.7.4.761. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- WOOD R. L. Intercellular attachment in the epithelium of Hydra as revealed by electron microscopy. J Biophys Biochem Cytol. 1959 Dec;6:343–352. doi: 10.1083/jcb.6.3.343. [DOI] [PMC free article] [PubMed] [Google Scholar]