Literature DB >> 7931550

Microtubule fragmentation and partitioning in the axon during collateral branch formation.

W Yu1, F J Ahmad, P W Baas.   

Abstract

Axons within the brain branch principally by the formation of collaterals rather than by bifurcation of the terminal growth cone (O'Leary and Terashima, 1988). This same behavior is recapitulated in cultures of embryonic hippocampal neurons (Dotti et al., 1988), rendering them ideal for studies on the cell biological mechanisms underlying collateral branch formation. In the present study, we focused on changes in the microtubule (MT) array that occur as these axons branch. In particular, we explored the mechanism by which MT number is locally increased to accommodate the need for more MTs during collateral branch formation. Serial reconstruction analyses indicate that MT number increases by severalfold and that MT length decreases correspondingly within the parent axon in the discrete region giving rise to the branch. These observations strongly suggest that MTs within the parent axon undergo a local fragmentation in this region, and hence raise the possibility that a portion of these new MTs might be destined for transport into the branch. To address this latter issue, we used quantitative immunofluorescence to compare the proportion of newly assembled to total MT polymer in different regions of the axon. As previously reported (Brown et al., 1992), the region of the axon contiguous with the terminal growth cone is particularly rich in newly assembled polymer. In contrast, there was no distinguishable difference in the proportion of newly assembled polymer in the newly formed collateral branches compared to the shaft region of the parent axon. These results indicate that the MTs within the newly formed collateral branches are on average assembled at the same time as those within the parent axon, and thus strongly suggest that the MTs in the collateral branch were assembled in the parent axon and then translocated into the branch. We conclude on the basis of these observations that collateral branch formation requires a local fragmentation of MTs within the parent axon, followed by the partitioning of a portion of the MT fragments into the branch. These short MTs presumably then resume their movement and elongation down the collateral branch as well as down the parent axon for the steady and orderly increase of both MT arrays.

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Year:  1994        PMID: 7931550      PMCID: PMC6576981     

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


  49 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

Review 2.  The elimination of accumulated and aggregated proteins: a role for aggrephagy in neurodegeneration.

Authors:  Ai Yamamoto; Anne Simonsen
Journal:  Neurobiol Dis       Date:  2010-08-20       Impact factor: 5.996

Review 3.  Developmental regulation of axon branching in the vertebrate nervous system.

Authors:  Daniel A Gibson; Le Ma
Journal:  Development       Date:  2011-01       Impact factor: 6.868

4.  Regulation of microtubule severing by katanin subunits during neuronal development.

Authors:  Wenqian Yu; Joanna M Solowska; Liang Qiang; Arzu Karabay; Douglas Baird; Peter W Baas
Journal:  J Neurosci       Date:  2005-06-08       Impact factor: 6.167

5.  The microtubule-severing proteins spastin and katanin participate differently in the formation of axonal branches.

Authors:  Wenqian Yu; Liang Qiang; Joanna M Solowska; Arzu Karabay; Sirin Korulu; Peter W Baas
Journal:  Mol Biol Cell       Date:  2008-01-30       Impact factor: 4.138

Review 6.  Microtubule-severing enzymes at the cutting edge.

Authors:  David J Sharp; Jennifer L Ross
Journal:  J Cell Sci       Date:  2012-05-17       Impact factor: 5.285

7.  The Roles of Microtubules and Membrane Tension in Axonal Beading, Retraction, and Atrophy.

Authors:  Anagha Datar; Jaishabanu Ameeramja; Alka Bhat; Roli Srivastava; Ashish Mishra; Roberto Bernal; Jacques Prost; Andrew Callan-Jones; Pramod A Pullarkat
Journal:  Biophys J       Date:  2019-08-02       Impact factor: 4.033

8.  Basic fibroblast growth factor increases functional L-type Ca2+ channels in fetal rat hippocampal neurons: implications for neurite morphogenesis in vitro.

Authors:  Y Shitaka; N Matsuki; H Saito; H Katsuki
Journal:  J Neurosci       Date:  1996-10-15       Impact factor: 6.167

9.  Dynamic organization of endocytic pathways in axons of cultured sympathetic neurons.

Authors:  C C Overly; P J Hollenbeck
Journal:  J Neurosci       Date:  1996-10-01       Impact factor: 6.167

10.  CNP/cGMP signaling regulates axon branching and growth by modulating microtubule polymerization.

Authors:  Caihong Xia; Minh Nguyen; Amy K Garrison; Zhen Zhao; Zheng Wang; Calum Sutherland; Le Ma
Journal:  Dev Neurobiol       Date:  2013-06-24       Impact factor: 3.964

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