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. 1986 Nov 1;103(5):1921–1931. doi: 10.1083/jcb.103.5.1921

Stages in axon formation: observations of growth of Aplysia axons in culture using video-enhanced contrast-differential interference contrast microscopy

PMCID: PMC2114395  PMID: 3782290

Abstract

The regenerative growth in culture of the axons of two giant identified neurons from the central nervous system of Aplysia californica was observed using video-enhanced contrast-differential interference contrast microscopy. This technique allowed the visualization in living cells of the membranous organelles of the growth cone. Elongation of axonal branches always occurred through the same sequence of events: A flat organelle-free veil protruded from the front of the growth cone, gradually filled with vesicles that entered by fast axonal transport and Brownian motion from the main body of the growth cone, became more voluminous and engorged with organelles (vesicles, mitochondria, and one or two large, irregular, refractile bodies), and, finally, assumed the cylindrical shape of the axon branch with the organelles predominantly moving by bidirectional fast axonal transport. The veil is thus the nascent axon. Because veils appear to be initially free of membranous organelles, addition of membrane to the plasmalemma by exocytosis is likely to occur in the main body of the growth cone rather than at the leading edge. Veils almost always formed with filopodial borders, protruding between either fully extended or growing filopodia. Therefore, one function of the filopodia is to direct elongation by demarcating the pathway along which axolemma flows. Models of axon growth in which the body of the growth cone is pulled forward, or in which advance of the leading edge is achieved by filopodial shortening or contraction against an adhesion to the substrate, are inconsistent with our observations. We suggest that, during the elongation phase of growth, filopodia may act as structural supports.

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Selected References

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  1. Allen R. D., Metuzals J., Tasaki I., Brady S. T., Gilbert S. P. Fast axonal transport in squid giant axon. Science. 1982 Dec 10;218(4577):1127–1129. doi: 10.1126/science.6183744. [DOI] [PubMed] [Google Scholar]
  2. Allen R. D. New observations on cell architecture and dynamics by video-enhanced contrast optical microscopy. Annu Rev Biophys Biophys Chem. 1985;14:265–290. doi: 10.1146/annurev.bb.14.060185.001405. [DOI] [PubMed] [Google Scholar]
  3. Anglister L., Farber I. C., Shahar A., Grinvald A. Localization of voltage-sensitive calcium channels along developing neurites: their possible role in regulating neurite elongation. Dev Biol. 1982 Dec;94(2):351–365. doi: 10.1016/0012-1606(82)90353-0. [DOI] [PubMed] [Google Scholar]
  4. Argiro V., Bunge M. B., Johnson M. I. Correlation between growth form and movement and their dependence on neuronal age. J Neurosci. 1984 Dec;4(12):3051–3062. doi: 10.1523/JNEUROSCI.04-12-03051.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bentley D., Caudy M. Navigational substrates for peripheral pioneer growth cones: limb-axis polarity cues, limb-segment boundaries, and guidepost neurons. Cold Spring Harb Symp Quant Biol. 1983;48(Pt 2):573–585. doi: 10.1101/sqb.1983.048.01.062. [DOI] [PubMed] [Google Scholar]
  6. Bray D., Bunge M. B. The growth cone in neurite extension. Ciba Found Symp. 1973;14:195–209. doi: 10.1002/9780470719978.ch9. [DOI] [PubMed] [Google Scholar]
  7. Bray D., Chapman K. Analysis of microspike movements on the neuronal growth cone. J Neurosci. 1985 Dec;5(12):3204–3213. doi: 10.1523/JNEUROSCI.05-12-03204.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Bray D. Mechanical tension produced by nerve cells in tissue culture. J Cell Sci. 1979 Jun;37:391–410. doi: 10.1242/jcs.37.1.391. [DOI] [PubMed] [Google Scholar]
  9. Bray D. Model for membrane movements in the neural growth cone. Nature. 1973 Jul 13;244(5411):93–96. doi: 10.1038/244093a0. [DOI] [PubMed] [Google Scholar]
  10. Bray D. Surface movements during the growth of single explanted neurons. Proc Natl Acad Sci U S A. 1970 Apr;65(4):905–910. doi: 10.1073/pnas.65.4.905. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Carbonetto S., Muller K. J. Nerve fiber growth and the cellular response to axotomy. Curr Top Dev Biol. 1982;17(Pt 3):33–76. doi: 10.1016/s0070-2153(08)60518-9. [DOI] [PubMed] [Google Scholar]
  12. Cheng T. P., Reese T. S. Polarized compartmentalization of organelles in growth cones from developing optic tectum. J Cell Biol. 1985 Oct;101(4):1473–1480. doi: 10.1083/jcb.101.4.1473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Dipasquale A. Locomotory activity of epithelial cells in culture. Exp Cell Res. 1975 Aug;94(1):191–215. doi: 10.1016/0014-4827(75)90545-5. [DOI] [PubMed] [Google Scholar]
  14. Edds K. T. The formation and elongation of filopodia during transformation of sea urchin coelomocytes. Cell Motil. 1980;1(1):131–140. doi: 10.1002/cm.970010110. [DOI] [PubMed] [Google Scholar]
  15. Griffin J. W., Price D. L., Drachman D. B., Morris J. Incorporation of axonally transported glycoproteins into axolemma during nerve regeneration. J Cell Biol. 1981 Jan;88(1):205–214. doi: 10.1083/jcb.88.1.205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hayden J. H., Allen R. D., Goldman R. D. Cytoplasmic transport in keratocytes: direct visualization of particle translocation along microtubules. Cell Motil. 1983;3(1):1–19. doi: 10.1002/cm.970030102. [DOI] [PubMed] [Google Scholar]
  17. Ingram V. M. A side view of moving fibroblasts. Nature. 1969 May 17;222(5194):641–644. doi: 10.1038/222641a0. [DOI] [PubMed] [Google Scholar]
  18. Koenig E., Kinsman S., Repasky E., Sultz L. Rapid mobility of motile varicosities and inclusions containing alpha-spectrin, actin, and calmodulin in regenerating axons in vitro. J Neurosci. 1985 Mar;5(3):715–729. doi: 10.1523/JNEUROSCI.05-03-00715.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Landis S. C. Neuronal growth cones. Annu Rev Physiol. 1983;45:567–580. doi: 10.1146/annurev.ph.45.030183.003031. [DOI] [PubMed] [Google Scholar]
  20. Letourneau P. C. Cell-substratum adhesion of neurite growth cones, and its role in neurite elongation. Exp Cell Res. 1979 Nov;124(1):127–138. doi: 10.1016/0014-4827(79)90263-5. [DOI] [PubMed] [Google Scholar]
  21. Lopresti V., Macagno E. R., Levinthal C. Structure and development of neuronal connections in isogenic organisms: cellular interactions in the development of the optic lamina of Daphnia. Proc Natl Acad Sci U S A. 1973 Feb;70(2):433–437. doi: 10.1073/pnas.70.2.433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Ludueña M. A., Wessells N. K. Cell locomotion, nerve elongation, and microfilaments. Dev Biol. 1973 Feb;30(2):427–440. doi: 10.1016/0012-1606(73)90100-0. [DOI] [PubMed] [Google Scholar]
  23. Marsh L., Letourneau P. C. Growth of neurites without filopodial or lamellipodial activity in the presence of cytochalasin B. J Cell Biol. 1984 Dec;99(6):2041–2047. doi: 10.1083/jcb.99.6.2041. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. NAKAI J. Dissociated dorsal root ganglia in tissue culture. Am J Anat. 1956 Jul;99(1):81–129. doi: 10.1002/aja.1000990105. [DOI] [PubMed] [Google Scholar]
  25. Nuttall R. P., Wessells N. K. Veils, mounds, and vesicle aggregates in neurons elongating in vitro. Exp Cell Res. 1979 Mar 1;119(1):163–174. doi: 10.1016/0014-4827(79)90345-8. [DOI] [PubMed] [Google Scholar]
  26. Pfenninger K. H., Maylié-Pfenninger M. F. Lectin labeling of sprouting neurons. II. Relative movement and appearance of glycoconjugates during plasmalemmal expansion. J Cell Biol. 1981 Jun;89(3):547–559. doi: 10.1083/jcb.89.3.547. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Roberts A., Taylor J. S. A study of the growth cones of developing embryonic sensory neurites. J Embryol Exp Morphol. 1983 Jun;75:31–47. [PubMed] [Google Scholar]
  28. Schacher S. Differential synapse formation and neurite outgrowth at two branches of the metacerebral cell of Aplysia in dissociated cell culture. J Neurosci. 1985 Aug;5(8):2028–2034. doi: 10.1523/JNEUROSCI.05-08-02028.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Schnapp B. J., Vale R. D., Sheetz M. P., Reese T. S. Single microtubules from squid axoplasm support bidirectional movement of organelles. Cell. 1985 Feb;40(2):455–462. doi: 10.1016/0092-8674(85)90160-6. [DOI] [PubMed] [Google Scholar]
  30. Seeley P. J., Greene L. A. Short-latency local actions of nerve growth factor at the growth cone. Proc Natl Acad Sci U S A. 1983 May;80(9):2789–2793. doi: 10.1073/pnas.80.9.2789. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Tosney K. W., Landmesser L. T. Growth cone morphology and trajectory in the lumbosacral region of the chick embryo. J Neurosci. 1985 Sep;5(9):2345–2358. doi: 10.1523/JNEUROSCI.05-09-02345.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Tosney K. W., Wessells N. K. Neuronal motility: the ultrastructure of veils and microspikes correlates with their motile activities. J Cell Sci. 1983 May;61:389–411. doi: 10.1242/jcs.61.1.389. [DOI] [PubMed] [Google Scholar]
  33. Trinkaus J. P. Further thoughts on directional cell movement during morphogenesis. J Neurosci Res. 1985;13(1-2):1–19. doi: 10.1002/jnr.490130102. [DOI] [PubMed] [Google Scholar]
  34. Wessells N. K., Spooner B. S., Ludueña M. A. Surface movements, microfilaments and cell locomotion. Ciba Found Symp. 1973;14:53–82. doi: 10.1002/9780470719978.ch4. [DOI] [PubMed] [Google Scholar]

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