Skip to main content
Journal of Anatomy logoLink to Journal of Anatomy
. 1977 Jul;123(Pt 3):763–775.

The structure and composition of peripheral nerves and nerve roots in the Sprawling mouse.

L W Duchen, F Scaravilli
PMCID: PMC1234733  PMID: 885789

Abstract

Peripheral nerves and lumbar nerve roots of Sprawling, a neurological mutant mouse, were examined with light and electron microscopy. The peripheral nerves and the dorsal roots were thin and grey and were composed predominantly of small myelinated and unmyelinated axons. No evidence of axonal or myelin degeneration was found. Quantitative studies showed a marked reduction in the total number of myelinated axons with preponderance of those of 2-5 micron in diameter or less, most marked in the dorsal roots in which there was also an increase in the proportion of axons which were unmyelinated. In the ventral roots there was a deficiency in the contribution formed by myelinated axons of small calibre, probably indicating a deficiency of gamma fibres. Examination of the myelinated axons in nerves and roots showed a normal relationship between fibre size and internodal lengths and number of myelin lamellae. The findings suggest that the genetic defect in Sprawling is responsible for a failure of myelination of sensory axons. The deficiency of large sensory axons and of small motor axons can be correlated with the deficiency of muscle spindles.

Full text

PDF
763

Images in this article

Selected References

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

  1. Andrews J. M. The fine structure of the cervical spinal cord, ventral root and brachial nerves in the wobbler (wr) mouse. J Neuropathol Exp Neurol. 1975 Jan;34(1):12–27. doi: 10.1097/00005072-197501000-00002. [DOI] [PubMed] [Google Scholar]
  2. Bradley W. G., Jenkison M. Abnormalities of peripheral nerves in murine muscular dystrophy. J Neurol Sci. 1973 Feb;18(2):227–247. doi: 10.1016/0022-510x(73)90009-9. [DOI] [PubMed] [Google Scholar]
  3. Bradley W. G., Jenkison M. Neural abnormalities in the dystrophic mouse. J Neurol Sci. 1975 Jun;25(2):249–255. doi: 10.1016/0022-510x(75)90144-6. [DOI] [PubMed] [Google Scholar]
  4. Coggeshall R. E., Coulter J. D., Willis W. D., Jr Unmyelinated axons in the ventral roots of the cat lumbosacral enlargement. J Comp Neurol. 1974 Jan 1;153(1):39–58. doi: 10.1002/cne.901530105. [DOI] [PubMed] [Google Scholar]
  5. DUCHEN L. W., STRICH S. J., FALCONER D. S. CLINICAL AND PATHOLOGICAL STUDIES OF AN HEREDITARY NEUROPATHY IN MICE (DYSTONIA MUSCULORUM). Brain. 1964 Jun;87:367–378. doi: 10.1093/brain/87.2.367. [DOI] [PubMed] [Google Scholar]
  6. Duchen L. W., Strich S. J. An hereditary motor neurone disease with progressive denervation of muscle in the mouse: the mutant 'wobbler'. J Neurol Neurosurg Psychiatry. 1968 Dec;31(6):535–542. doi: 10.1136/jnnp.31.6.535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dyck P. J., Lais A. C. Electron microscopy of teased nerve fibers: method permitting examination of repeating structures of same fiber. Brain Res. 1970 Oct 28;23(3):418–424. doi: 10.1016/0006-8993(70)90067-3. [DOI] [PubMed] [Google Scholar]
  8. GAMBLE H. J. COMPARATIVE ELECTRON-MICROSCOPIC OBSERVATIONS ON THE CONNECTIVE TISSUES OF A PERIPHERAL NERVE AND A SPINAL NERVE ROOT IN THE RAT. J Anat. 1964 Jan;98:17–26. [PMC free article] [PubMed] [Google Scholar]
  9. Hughes J. T., Brownell B., Hewer R. L. The peripheral sensory pathway in friedreich's ataxia. An examination by light and electron microscopy of the posterior nerve roots, posterior root ganglia, and peripheral sensory nerves in cases of friedreich's ataxia. Brain. 1968;91(4):803–818. doi: 10.1093/brain/91.4.803. [DOI] [PubMed] [Google Scholar]
  10. Janota I. Ultrastructural studies of an hereditary sensory neuropathy in mice (dystonia musculorum). Brain. 1972;95(3):529–536. doi: 10.1093/brain/95.3.529. [DOI] [PubMed] [Google Scholar]
  11. NATHANIEL E. J., PEASE D. C. REGENERATIVE CHANGES IN RAT DORSAL ROOTS FOLLOWING WALERIAN DEGENERATION. J Ultrastruct Res. 1963 Dec;52:533–549. doi: 10.1016/s0022-5320(63)80083-0. [DOI] [PubMed] [Google Scholar]
  12. Nathaniel E. J., Nathaniel D. R. Regeneration of dorsal root fibers into the adult rat spinal cord. Exp Neurol. 1973 Aug;40(2):333–350. doi: 10.1016/0014-4886(73)90078-2. [DOI] [PubMed] [Google Scholar]
  13. Ochoa J., Mair W. G. The normal sural nerve in man. I. Ultrastructure and numbers of fibres and cells. Acta Neuropathol. 1969;13(3):197–216. doi: 10.1007/BF00690642. [DOI] [PubMed] [Google Scholar]
  14. Salafsky B., Stirling C. A. Altered neural protein in murine muscular dystrophy. Nat New Biol. 1973 Nov 28;246(152):126–128. doi: 10.1038/newbio246126a0. [DOI] [PubMed] [Google Scholar]
  15. Samorajski T., Rolsten C. Nerve fiber hypertrophy in posterior tibial nerves of mice in response to voluntary running activity during aging. J Comp Neurol. 1975 Feb 15;159(4):553–558. doi: 10.1002/cne.901590407. [DOI] [PubMed] [Google Scholar]
  16. Schröder J. M. Altered ratio between axon diameter and myelin sheath thickness in regenerated nerve fibers. Brain Res. 1972 Oct 13;45(1):49–65. doi: 10.1016/0006-8993(72)90215-6. [DOI] [PubMed] [Google Scholar]
  17. Stirling C. A. Abnormalities in Schwann cell sheaths in spinal nerve roots of dystrophic mice. J Anat. 1975 Feb;119(Pt 1):169–180. [PMC free article] [PubMed] [Google Scholar]
  18. Sykes M. T., Coggeshall R. E. Unmyelinated fibers in the human L4 and L5 ventral roots. Brain Res. 1973 Dec 7;63:490–495. doi: 10.1016/0006-8993(73)90130-3. [DOI] [PubMed] [Google Scholar]
  19. Vizoso A. D., Young J. Z. Internode length and fibre diameter in developing and regenerating nerves. J Anat. 1948 Apr;82(Pt 1-2):110–134.1. [PMC free article] [PubMed] [Google Scholar]
  20. ZELENA J. DEVELOPMENT, DEGENERATION AND REGENERATION OF RECEPTOR ORGANS. Prog Brain Res. 1964;13:175–213. [PubMed] [Google Scholar]

Articles from Journal of Anatomy are provided here courtesy of Anatomical Society of Great Britain and Ireland

RESOURCES