Literature DB >> 10516309

Reorganization and movement of microtubules in axonal growth cones and developing interstitial branches.

E W Dent1, J L Callaway, G Szebenyi, P W Baas, K Kalil.   

Abstract

Local changes in microtubule organization and distribution are required for the axon to grow and navigate appropriately; however, little is known about how microtubules (MTs) reorganize during directed axon outgrowth. We have used time-lapse digital imaging of developing cortical neurons microinjected with fluorescently labeled tubulin to follow the movements of individual MTs in two regions of the axon where directed growth occurs: the terminal growth cone and the developing interstitial branch. In both regions, transitions from quiescent to growth states were accompanied by reorganization of MTs from looped or bundled arrays to dispersed arrays and fragmentation of long MTs into short MTs. We also found that long-term redistribution of MTs accompanied the withdrawal of some axonal processes and the growth and stabilization of others. Individual MTs moved independently in both anterograde and retrograde directions to explore developing processes. Their velocities were inversely proportional to their lengths. Our results demonstrate directly that MTs move within axonal growth cones and developing interstitial branches. Our findings also provide the first direct evidence that similar reorganization and movement of individual MTs occur in the two regions of the axon where directed outgrowth occurs. These results suggest a model whereby short exploratory MTs could direct axonal growth cones and interstitial branches toward appropriate locations.

Mesh:

Year:  1999        PMID: 10516309      PMCID: PMC6782770     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  61 in total

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Journal:  Trends Cell Biol       Date:  1997-10       Impact factor: 20.808

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Journal:  Neuron       Date:  1995-06       Impact factor: 17.173

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Authors:  V I Rodionov; G G Borisy
Journal:  Science       Date:  1997-01-10       Impact factor: 47.728

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Authors:  N Yamamoto; S Higashi; K Toyama
Journal:  J Neurosci       Date:  1997-05-15       Impact factor: 6.167

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Authors:  I G McQuarrie; S T Brady; R J Lasek
Journal:  J Neurosci       Date:  1986-06       Impact factor: 6.167

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Journal:  J Neurocytol       Date:  1987-12

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Journal:  Cell Motil Cytoskeleton       Date:  1993

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Authors:  D M Suter; L D Errante; V Belotserkovsky; P Forscher
Journal:  J Cell Biol       Date:  1998-04-06       Impact factor: 10.539

9.  Cytoplasmic dynein and dynactin are required for the transport of microtubules into the axon.

Authors:  F J Ahmad; C J Echeverri; R B Vallee; P W Baas
Journal:  J Cell Biol       Date:  1998-01-26       Impact factor: 10.539

10.  Cytoskeletal remodeling during growth cone-target interactions.

Authors:  C H Lin; P Forscher
Journal:  J Cell Biol       Date:  1993-06       Impact factor: 10.539

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  89 in total

1.  Self-organization of a radial microtubule array by dynein-dependent nucleation of microtubules.

Authors:  I Vorobjev; V Malikov; V Rodionov
Journal:  Proc Natl Acad Sci U S A       Date:  2001-08-14       Impact factor: 11.205

2.  Axon branching requires interactions between dynamic microtubules and actin filaments.

Authors:  E W Dent; K Kalil
Journal:  J Neurosci       Date:  2001-12-15       Impact factor: 6.167

Review 3.  Retrograde signaling at central synapses.

Authors:  H W Tao; M Poo
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-25       Impact factor: 11.205

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Authors:  I E Vega; S C Hsu
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

5.  Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport.

Authors:  S Roy; P Coffee; G Smith; R K Liem; S T Brady; M M Black
Journal:  J Neurosci       Date:  2000-09-15       Impact factor: 6.167

6.  Visualization of microtubule growth in cultured neurons via the use of EB3-GFP (end-binding protein 3-green fluorescent protein).

Authors:  Tatiana Stepanova; Jenny Slemmer; Casper C Hoogenraad; Gideon Lansbergen; Bjorn Dortland; Chris I De Zeeuw; Frank Grosveld; Gert van Cappellen; Anna Akhmanova; Niels Galjart
Journal:  J Neurosci       Date:  2003-04-01       Impact factor: 6.167

7.  The Drosophila Wnt, wingless, provides an essential signal for pre- and postsynaptic differentiation.

Authors:  Mary Packard; Ellen Sumin Koo; Michael Gorczyca; Jade Sharpe; Susan Cumberledge; Vivian Budnik
Journal:  Cell       Date:  2002-11-01       Impact factor: 41.582

8.  Fibroblast growth factor-2 promotes axon branching of cortical neurons by influencing morphology and behavior of the primary growth cone.

Authors:  G Szebenyi; E W Dent; J L Callaway; C Seys; H Lueth; K Kalil
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

9.  Spontaneous calcium transients in developing cortical neurons regulate axon outgrowth.

Authors:  Fangjun Tang; Erik W Dent; Katherine Kalil
Journal:  J Neurosci       Date:  2003-02-01       Impact factor: 6.167

10.  Tensile force-dependent neurite elicitation via anti-beta1 integrin antibody-coated magnetic beads.

Authors:  Joseph N Fass; David J Odde
Journal:  Biophys J       Date:  2003-07       Impact factor: 4.033

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