Bundling of microtubules in the growth cone induced by laminin

Molecular and Cellular Neurosciences

Volumn 15, Issue 3, 2000, Pages 303-313

  Tang, Dongjiang ^a   Goldberg, Daniel J ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN; LAMININ;

ACTIN FILAMENT; ANIMAL TISSUE; ARTICLE; CYTOSKELETON; EXTRACELLULAR MATRIX; GROWTH CONE; IMMUNOCYTOCHEMISTRY; MICROTUBULE; NERVE FIBER GROWTH; NERVOUS SYSTEM DEVELOPMENT; NEURITE; NONHUMAN; PRIORITY JOURNAL; RAT; SYMPATHETIC NERVE CELL;

ANIMALIA;

EID: 0034106441     PISSN: 10447431     EISSN: None     Source Type: Journal    
DOI: 10.1006/mcne.1999.0820     Document Type: Article

References (42)

1. Aigner L., Caroni P. Depletion of 43-kD growth-associated protein in primary sensory neurons leads to diminished formation and spreading of growth cones. J. Cell Biol. 123:1993;417-429.
2. Aletta J. M., Lewis S. A., Cowan N. J., Greene L. A. Nerve growth factor regulates both the phosphorylation and steady-state levels of microtubule-associated protein 1.2 (MAP1.2). J. Cell Biol. 106:1988;1573-1581.
3. Bentley D., Toroian-Raymond A. Disoriented pathfinding by pioneer neurone growth cones deprived of filopodia by cytochalasin treatment. Nature. 323:1986;712-715.
4. Black M. M., Aletta J. M., Greene L. A. Regulation of microtubule composition and stability during nerve growth factor-promoted neurite outgrowth. J. Cell Biol. 103:1986;545-557.
5. Black M. M., Slaughter T., Fischer I. Microtubule-associated protein 1b (MAP1b) is concentrated in the distal region of growing axons. J. Neurosci. 14:1994;857-870.
6. Bozyczko D., Horwitz A. F. The participation of a putative cell surface receptor for laminin and fibronectin in peripheral neurite extension. J. Neurosci. 6:1986;1241-1251.
7. Bradke F., Dotti C. G. Neuronal polarity: Vectorial cytoplasmic flow precedes axon formation. Neuron. 19:1997;1175-1186.
8. Burden-Gulley S. M., Lemmon V. L1, N-cadherin, and laminin induce distinct distribution patterns of cytoskeletal elements in growth cones. Cell Motil. Cytoskeleton. 35:1996;1-23.
9. Burridge K., Fath K., Kelly T., Nuckolls G., Turner C. Focal adhesions: Transmembrane junctions between the extracellular matrix and the cytoskeleton. Annu. Rev. Cell Biol. 4:1988;487-525.
10. Challacombe J. F., Snow D. M., Letourneau P. C. Actin filament bundles are required for microtubule reorientation during growth cone turning to avoid an inhibitory guidance cue. J. Cell Sci. 109:1996;2031-2040.
11. DiTella M. C., Feiguin F., Carri N., Kosik K. S., Cáceras A. MAP-1B/tau functional redundancy during laminin-enhanced axonal growth. J. Cell Sci. 109:1996;467-477.
12. Fan J., Mansfield S. G., Redmond T., Gordon-Weeks P. R., Raper J. The organization of F-actin and microtubules in growth cones exposed to a brain-derived collapsing factor. J. Cell Biol. 121:1993;867-878.
13. Felsenfeld D. P., Choquet D., Sheetz M. P. Ligand binding regulates the directed movement of β1 integrins on fibroblasts. Nature. 383:1996;438-440.
14. Forscher P., Smith S. J. Actions of cytochalasins on the organization of actin filaments and microtubules in a neuronal growth cone. J. Cell Biol. 107:1988;1505-1516.
15. Goldberg D. J., Burmeister D. W. Looking into growth cones. Trends Neurosci. 12:1989;503-506.
16. Goodman C. S. Mechanisms and molecules that control growth cone guidance. Annu. Rev. Neurosci. 19:1996;341-377.
17. Goslin K., Banker G. Experimental observations on the development of polarity by hippocampal neurons in culture. J. Cell Biol. 108:1989;1507-1516.
18. Goslin K., Banker G. Rapid changes in the distribution of GAP-43 correlate with the expression of neuronal polarity during normal development and under experimental conditions. J. Cell Biol. 110:1990;1319-1331.
19. Grabham P. W., Goldberg D. J. Nerve growth factor stimulates the accumulation of β1 integrin at the tips of filopodia in the growth cones of sympathetic neurons. J. Neurosci. 17:1997;5455-5465.
20. Hynes R. O., Destree A. T. Relationships between fibronectin (LETS protein) and actin. Cell. 15:1978;875-886.
21. Kaethner R. J., Stuermer C. A. O. Dynamics of terminal arbor formation and target approach of retinotectal axons in living zebrafish embryos: A time-lapse study of single axons. J. Neurosci. 12:1992;3257-3271.
22. Kuhn T. B., Schmidt M. F., Kater S. B. Laminin and fibronectin guideposts signal sustained but opposite effects to passing growth cones. Neuron. 14:1995;275-285.
23. Kuhn T. B., Williams C. V., Dou P., Kater S. B. Laminin directs growth cone navigation via two temporally and functionally distinct calcium signals. J. Neurosci. 18:1998;184-194.
24. Lander A. Molecules that make axons grow. Mol. Neurobiol. 1:1987;213-245.
25. Lein P. J., Higgins D. Laminin and a basement membrane extract have different effects on axonal and dendritic outgrowth from embryonic rat sympathetic neurons in vitro. Dev. Biol. 136:1989;330-345.
26. Lentz S. I., Miner J. H., Sanes J. R., Snider W. D. Distribution of the ten known laminin chains in the pathways and targets of developing sensory axons. J. Comp. Neurol. 378:1997;547-561.
27. Letourneau P. C. Differences in the organization of actin in the growth cones compared with the neurites of cultured neurons from chick embryos. J. Cell Biol. 97:1983;963-973.
28. Letourneau P. C., Shattuck T. A., Ressler A. H. "Pull" and "push" in neurite elongation: Observations on the effects of different concentrations of cytochalasin B and Taxol. Cell Motil. Cytoskeleton. 8:1987;193-209.
29. Lewis A. K., Bridgman P. C. Mammalian myosin Iα is concentrated near the plasma membrane in nerve growth cones. Cell Motil. Cytoskeleton. 33:1996;130-150.
30. Lin C.-H., Forscher P. Cytoskeletal remodeling during growth cone-target interactions. J. Cell Biol. 121:1993;1369-1383.
31. 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. USA. 70:1973;433-437.
32. Mooney D. J., Langer R., Ingber D. E. Cytoskeletal filament assembly and the control of cell spreading and function by extracellular matrix. J. Cell Sci. 108:1995;2311-2320.
33. Patton B. L., Miner J. H., Chiu A. Y., Sanes J. R. Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant mice. J. Cell Biol. 139:1997;1507-1521.
34. Reichardt L. F., Tomaselli K. J. Extracellular matrix molecules and their receptors: Functions in neural development. Annu. Rev. Neurosci. 14:1991;531-570.
35. Rivas R. J., Burmeister D. W., Goldberg D. J. Rapid effects of laminin on the growth cone. Neuron. 8:1992;107-115.
36. Seeley P. J., Greene L. A. Short-latency local actions of nerve growth factor at the growth cone. Proc Natl. Acad. Sci. USA. 80:1983;2789-2793.
37. Suter D. M., Errante L. D., Belotserkovsky V., Forscher P. The Ig superfamily cell adhesion molecule, apCAM, mediates growth cone steering by substrate-cytoskeletal coupling. J. Cell Biol. 141:1998;227-240.
38. Tanaka E. M., Ho T., Kirschner M. W. The role of microtubule dynamics in growth cone motility and axonal growth. J. Cell Biol. 128:1995;139-155.
39. Tanaka E. M., Kirschner M. W. Microtubule behavior in the growth cones of living neurons during axon elongation. J. Cell Biol. 115:1991;345-363.
40. Tanaka E. M., Kirschner M. W. The role of microtubules in growth cone turning at substrate boundaries. J. Cell Biol. 128:1995;127-137.
41. Tomaselli K. J., Damsky C. H., Reichardt L. F. Interactions of a neuronal cell line (PC12) with laminin, collagen IV, and fibronectin: Identification of integrin-related glycoproteins involved in attachment and process outgrowth. J. Cell Biol. 105:1987;2347-2358.
42. Yu W., Baas P. W. Changes in microtubule number and length during axon differentiation. J. Neurosci. 14:1994;2818-2829.