Literature DB >> 8182441

Changes in microtubule number and length during axon differentiation.

W Yu1, P W Baas.   

Abstract

Hippocampal neurons in culture initially extend several minor processes that are approximately 20 microns in length. The first minor process to grow approximately 10 microns longer than the others will continue to grow rapidly and become the axon (Goslin and Banker, 1989). We sought to define changes in the microtubule (MT) array that occur during axon differentiation. In theory, axon differentiation could involve an increase in MT number, MT length, or some combination of both. To address this issue, we first serially reconstructed the entire MT array of a minor process from a cell whose axon had not yet differentiated. This minor process contained 182 MTs that ranged in length from 0.14 to 20.09 microns. The average MT length was 3.87 +/- 3.83 microns, and the total MT length was 704 microns. We then reconstructed the MT arrays of a minor process and the 56 microns axon from a cell that had undergone axon differentiation. The minor process contained 157 MTs that ranged in length from 0.24 to 17.95 microns. The average MT length was 3.91 +/- 4.84 microns, and the total MT length was 600 microns. The axon contained 1430 MTs that ranged in length from 0.05 to 40.14 microns. The average MT length was 4.02 +/- 5.28 microns, and the total MT length was 5750 microns. These data indicate that a shift occurs toward shorter as well as longer MTs, but that virtually no change in average MT length occurs during axon differentiation. Thus, elongation of existing MTs cannot account for the major expansion of the MT array that occurs as a minor process becomes an axon. In contrast, the number of MTs increases by approximately 10-fold as a minor process differentiates and grows into an axon of the length we analyzed. Based on these data, we conclude that the MT array of a minor process is substantially expanded as it differentiates into an axon, and that the principal mechanism by which this expansion occurs is the copious addition of new MTs.

Mesh:

Year:  1994        PMID: 8182441      PMCID: PMC6577472     

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


  67 in total

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

Authors:  E W Dent; J L Callaway; G Szebenyi; P W Baas; K Kalil
Journal:  J Neurosci       Date:  1999-10-15       Impact factor: 6.167

2.  Growth cones are not required for initial establishment of polarity or differential axon branch growth in cultured hippocampal neurons.

Authors:  G Ruthel; P J Hollenbeck
Journal:  J Neurosci       Date:  2000-03-15       Impact factor: 6.167

3.  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

4.  Partial interruption of axonal transport due to microtubule breakage accounts for the formation of periodic varicosities after traumatic axonal injury.

Authors:  Min D Tang-Schomer; Victoria E Johnson; Peter W Baas; William Stewart; Douglas H Smith
Journal:  Exp Neurol       Date:  2011-11-04       Impact factor: 5.330

5.  Uniform polarity microtubule assemblies imaged in native brain tissue by second-harmonic generation microscopy.

Authors:  Daniel A Dombeck; Karl A Kasischke; Harshad D Vishwasrao; Martin Ingelsson; Bradley T Hyman; Watt W Webb
Journal:  Proc Natl Acad Sci U S A       Date:  2003-05-23       Impact factor: 11.205

6.  The nucleotide-binding state of microtubules modulates kinesin processivity and the ability of Tau to inhibit kinesin-mediated transport.

Authors:  Derrick P McVicker; Lynn R Chrin; Christopher L Berger
Journal:  J Biol Chem       Date:  2011-10-27       Impact factor: 5.157

7.  Computational modeling of axonal microtubule bundles under tension.

Authors:  Stephen J Peter; Mohammad R K Mofrad
Journal:  Biophys J       Date:  2012-02-21       Impact factor: 4.033

8.  Strategies for diminishing katanin-based loss of microtubules in tauopathic neurodegenerative diseases.

Authors:  Haruka Sudo; Peter W Baas
Journal:  Hum Mol Genet       Date:  2010-11-30       Impact factor: 6.150

9.  Acetylation of microtubules influences their sensitivity to severing by katanin in neurons and fibroblasts.

Authors:  Haruka Sudo; Peter W Baas
Journal:  J Neurosci       Date:  2010-05-26       Impact factor: 6.167

10.  Transglutaminase and polyamination of tubulin: posttranslational modification for stabilizing axonal microtubules.

Authors:  Yuyu Song; Laura L Kirkpatrick; Alexander B Schilling; Donald L Helseth; Nicolas Chabot; Jeffrey W Keillor; Gail V W Johnson; Scott T Brady
Journal:  Neuron       Date:  2013-04-10       Impact factor: 17.173

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