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. 1974 Apr 1;61(1):56–69. doi: 10.1083/jcb.61.1.56

MIGRATORY CELL LOCOMOTION VERSUS NERVE AXON ELONGATION

Differences Based on the Effects of Lanthanum Ion

Paul C Letourneau 1, Norman K Wessells 1
PMCID: PMC2109261  PMID: 4819307

Abstract

The effects of lanthanum ions (La+++) on the locomotion and adhesion of g lial cells and elongating nerve axons are reported. La+++ increases adhesion of both glia and of nerve growth cones to a plastic substratum. La+++ also markedly reduces glia locomotion, but it does not inhibit nerve elongation. Electron-opaque deposits are seen on the cell surface and within cytoplasmic vesicles of glia and nerves cultured in a La+++-containing medium. Possible modes of action for La+++ are discussed, particularly the possibilities that Ca++ fluxes or Ca++ involvement in adhesion are altered by La+++. The results are consistent with the hypothesis that cell migration and nerve axon elongation differ in mechanism, with respect to both adhesive interactions and the activity of microfilament systems.

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Selected References

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  1. Adelstein R. S., Conti M. A., Johnson G. S., Pastan I., Pollard T. D. Isolation and characterization of myosin from cloned mouse fibroblasts. Proc Natl Acad Sci U S A. 1972 Dec;69(12):3693–3697. doi: 10.1073/pnas.69.12.3693. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bray D. Branching patterns of individual sympathetic neurons in culture. J Cell Biol. 1973 Mar;56(3):702–712. doi: 10.1083/jcb.56.3.702. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. 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]
  4. Bunge M. B. Fine structure of nerve fibers and growth cones of isolated sympathetic neurons in culture. J Cell Biol. 1973 Mar;56(3):713–735. doi: 10.1083/jcb.56.3.713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DOGGENWEILER C. F., FRENK S. STAINING PROPERTIES OF LANTHANUM ON CELL MEMBRANES. Proc Natl Acad Sci U S A. 1965 Feb;53:425–430. doi: 10.1073/pnas.53.2.425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Fitzpatrick D. F., Landon E. J., Debbas G., Hurwitz L. A calcium pump in vascular smooth muscle. Science. 1972 Apr 21;176(4032):305–306. doi: 10.1126/science.176.4032.305. [DOI] [PubMed] [Google Scholar]
  7. Foreman J. C., Mongar J. L. Dual effect of lanthanum on histamine release from mast cells. Nat New Biol. 1972 Dec 20;240(103):255–256. doi: 10.1038/newbio240255a0. [DOI] [PubMed] [Google Scholar]
  8. Gail M. H., Boone C. W. The locomotion of mouse fibroblasts in tissue culture. Biophys J. 1970 Oct;10(10):980–993. doi: 10.1016/S0006-3495(70)86347-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. HUXLEY H., HANSON J. Changes in the cross-striations of muscle during contraction and stretch and their structural interpretation. Nature. 1954 May 22;173(4412):973–976. doi: 10.1038/173973a0. [DOI] [PubMed] [Google Scholar]
  10. Hawkes R. B., Holberton D. V. A calcium-sensitive lanthanum inhibition of amoeboid movement. J Cell Physiol. 1973 Jun;81(3):365–370. doi: 10.1002/jcp.1040810309. [DOI] [PubMed] [Google Scholar]
  11. Hurwitz L., Fitzpatrick D. F., Debbas G., Landon E. J. Localization of calcium pump activity in smooth muscle. Science. 1973 Jan 26;179(4071):384–386. doi: 10.1126/science.179.4071.384. [DOI] [PubMed] [Google Scholar]
  12. Huxley H. E. Muscular contraction and cell motility. Nature. 1973 Jun 22;243(5408):445–449. doi: 10.1038/243445a0. [DOI] [PubMed] [Google Scholar]
  13. 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]
  14. Langer G. A., Frank J. S. Lanthanum in heart cell culture. Effect on calcium exchange correlated with its localization. J Cell Biol. 1972 Sep;54(3):441–455. doi: 10.1083/jcb.54.3.441. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Langer G. A. Heart: excitation-contraction coupling. Annu Rev Physiol. 1973;35:55–86. doi: 10.1146/annurev.ph.35.030173.000415. [DOI] [PubMed] [Google Scholar]
  16. Lee K. S., Shin B. C. Studies on the active transport of calcium in human red cells. J Gen Physiol. 1969 Dec;54(6):713–729. doi: 10.1085/jgp.54.6.713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Ludueña M. A. Nerve cell differentiation in vitro. Dev Biol. 1973 Aug;33(2):268–284. doi: 10.1016/0012-1606(73)90137-1. [DOI] [PubMed] [Google Scholar]
  18. Ludueña M. A. The growth of spinal ganglion neurons in serum-free medium. Dev Biol. 1973 Aug;33(2):470–476. doi: 10.1016/0012-1606(73)90152-8. [DOI] [PubMed] [Google Scholar]
  19. 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]
  20. McIntosh J. R. The axostyle of Saccinobaculus. II. Motion of the microtubule bundle and a structural comparison of straight and bent axostyles. J Cell Biol. 1973 Feb;56(2):324–339. doi: 10.1083/jcb.56.2.324. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Mooseker M. S., Tilney L. G. Isolation and reactivation of the axostyle. Evidence for a dynein-like ATPase in the axostyle. J Cell Biol. 1973 Jan;56(1):13–26. doi: 10.1083/jcb.56.1.13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Murakami A., Eckert R. Cilia: activation coupled to mechanical stimulation by calcium influx. Science. 1972 Mar 24;175(4028):1375–1377. doi: 10.1126/science.175.4028.1375. [DOI] [PubMed] [Google Scholar]
  23. Naito Y., Kaneko H. Reactivated triton-extracted models o paramecium: modification of ciliary movement by calcium ions. Science. 1972 May 5;176(4034):523–524. doi: 10.1126/science.176.4034.523. [DOI] [PubMed] [Google Scholar]
  24. Pinto da Silva P., Branton D. Membrane splitting in freeze-ethching. Covalently bound ferritin as a membrane marker. J Cell Biol. 1970 Jun;45(3):598–605. doi: 10.1083/jcb.45.3.598. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Sandow A. Skeletal muscle. Annu Rev Physiol. 1970;32:87–138. doi: 10.1146/annurev.ph.32.030170.000511. [DOI] [PubMed] [Google Scholar]
  26. Somlyo A. V., Somlyo A. P. Strontium accumulation by sarcoplasmic reticulum and mitochondria in vascular smooth muscle. Science. 1971 Nov 26;174(4012):955–958. doi: 10.1126/science.174.4012.955. [DOI] [PubMed] [Google Scholar]
  27. Spooner B. S. The expression of differentiation by chick embryo thyroid in cell culture. I. Functional and fine structural stability in mass and clonal culture. J Cell Physiol. 1970 Feb;75(1):33–47. doi: 10.1002/jcp.1040750105. [DOI] [PubMed] [Google Scholar]
  28. Strassman R. J., Letourneau P. C., Wessells N. K. Elongation of axons in an agar matrix that does not support cell locomotion. Exp Cell Res. 1973 Oct;81(2):482–487. doi: 10.1016/0014-4827(73)90539-9. [DOI] [PubMed] [Google Scholar]
  29. Summers K. E., Gibbons I. R. Adenosine triphosphate-induced sliding of tubules in trypsin-treated flagella of sea-urchin sperm. Proc Natl Acad Sci U S A. 1971 Dec;68(12):3092–3096. doi: 10.1073/pnas.68.12.3092. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Takata M., Pickard W. F., Lettvin J. Y., Moore J. W. Ionic conductance changes in lobster axon membrane when lanthanum is substituted for calcium. J Gen Physiol. 1966 Nov;50(2):461–471. doi: 10.1085/jgp.50.2.461. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Van Breemen C. Permselectivity of a porous phospholipid-cholesterol artificial membrane. Calcium and lanthanum effects. Biochem Biophys Res Commun. 1968 Sep 30;32(6):977–983. doi: 10.1016/0006-291x(68)90124-1. [DOI] [PubMed] [Google Scholar]
  32. Yamada K. M., Spooner B. S., Wessells N. K. Ultrastructure and function of growth cones and axons of cultured nerve cells. J Cell Biol. 1971 Jun;49(3):614–635. doi: 10.1083/jcb.49.3.614. [DOI] [PMC free article] [PubMed] [Google Scholar]

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