Literature DB >> 8613759

Three distinct axonal transport rates for tau, tubulin, and other microtubule-associated proteins: evidence for dynamic interactions of tau with microtubules in vivo.

M Mercken1, I Fischer, K S Kosik, R A Nixon.   

Abstract

Microtubule-associated proteins (MAPs), such as tau, modulate neuronal shape and process outgrowth by influencing the stability and organization of microtubules. The dynamic nature of MAP-microtubule interactions in vivo, however, is poorly understood. Here, we have assessed the stability of these interactions by investigating the synthesis and axoplasmic transport of tau in relation to that of tubulin and other MAPs within retinal ganglion cells of normal adult mice in vivo. Using immunoprecipitation and Western blot analysis with anti-tau monoclonal and polyclonal antibodies, we unequivocally identified in optic axons a family of 50-60 kDa tau isoforms and a second 90-95 KDa tau family, the members of which were shown to contain the domain of tau encoded by exon 4A. To measure the rates of translocation of tau proteins in vivo, we injected mice with 35S-methionine intravitreously and, after 6-30 d, quantitated the radiolabeled tau isoforms immunoprecipitated from eight consecutive 1.1 mm segments of the nerve and optic tract and separated by electrophoresis. Linear regression analysis of protein transport along optic axons showed that the tau isoforms advanced at a rate of 0.2-0.4 mm/d, and other radiolabeled MAPs, identified by their association with taxol-stabilized microtubules, moved three- to fivefold more rapidly. By contrast, tubulins advanced at 0.1-0.2 mm/d, significantly more slowly than tau or other MAPs. These studies establish that tau is not cotransported with tubulin or microtubules, indicating that associations of tau with microtubules within axons are not as stable as previously believed. Our findings also reveal differences among various MAPs in their interactions with microtubules and provide evidence that assembly and reorganization of the microtubule network is an active process even after axons establish connections and fully mature.

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Year:  1995        PMID: 8613759      PMCID: PMC6577949     

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


  30 in total

1.  Axonal transport of microtubule-associated protein 1B (MAP1B) in the sciatic nerve of adult rat: distinct transport rates of different isoforms.

Authors:  D Ma; B T Himes; T B Shea; I Fischer
Journal:  J Neurosci       Date:  2000-03-15       Impact factor: 6.167

2.  Solution structure of the kinase-associated domain 1 of mouse microtubule-associated protein/microtubule affinity-regulating kinase 3.

Authors:  Naoya Tochio; Seizo Koshiba; Naohiro Kobayashi; Makoto Inoue; Takashi Yabuki; Masaaki Aoki; Eiko Seki; Takayoshi Matsuda; Yasuko Tomo; Yoko Motoda; Atsuo Kobayashi; Akiko Tanaka; Yoshihide Hayashizaki; Takaho Terada; Mikako Shirouzu; Takanori Kigawa; Shigeyuki Yokoyama
Journal:  Protein Sci       Date:  2006-11       Impact factor: 6.725

3.  Axonal transport rates in vivo are unaffected by tau deletion or overexpression in mice.

Authors:  Aidong Yuan; Asok Kumar; Corrinne Peterhoff; Karen Duff; Ralph A Nixon
Journal:  J Neurosci       Date:  2008-02-13       Impact factor: 6.167

Review 4.  Neuroproteomics as a promising tool in Parkinson's disease research.

Authors:  Ilse S Pienaar; William M U Daniels; Jürgen Götz
Journal:  J Neural Transm (Vienna)       Date:  2008-06-04       Impact factor: 3.575

5.  Fast vesicle transport is required for the slow axonal transport of synapsin.

Authors:  Yong Tang; David Scott; Utpal Das; Daniel Gitler; Archan Ganguly; Subhojit Roy
Journal:  J Neurosci       Date:  2013-09-25       Impact factor: 6.167

6.  Tau protein diffuses along the microtubule lattice.

Authors:  Maike H Hinrichs; Avesta Jalal; Bernhard Brenner; Eckhard Mandelkow; Satish Kumar; Tim Scholz
Journal:  J Biol Chem       Date:  2012-09-27       Impact factor: 5.157

7.  Cytoskeletal requirements in axonal transport of slow component-b.

Authors:  Subhojit Roy; Matthew J Winton; Mark M Black; John Q Trojanowski; Virginia M-Y Lee
Journal:  J Neurosci       Date:  2008-05-14       Impact factor: 6.167

8.  PSF suppresses tau exon 10 inclusion by interacting with a stem-loop structure downstream of exon 10.

Authors:  Payal Ray; Amar Kar; Kazuo Fushimi; Necat Havlioglu; Xiaoping Chen; Jane Y Wu
Journal:  J Mol Neurosci       Date:  2011-09-01       Impact factor: 3.444

9.  Pathological missorting of endogenous MAPT/Tau in neurons caused by failure of protein degradation systems.

Authors:  Varun Balaji; Senthilvelrajan Kaniyappan; Eckhard Mandelkow; Yipeng Wang; Eva-Maria Mandelkow
Journal:  Autophagy       Date:  2018-09-13       Impact factor: 16.016

10.  In vivo turnover of tau and APP metabolites in the brains of wild-type and Tg2576 mice: greater stability of sAPP in the beta-amyloid depositing mice.

Authors:  Jose Morales-Corraliza; Matthew J Mazzella; Jason D Berger; Nicole S Diaz; Jennifer H K Choi; Efrat Levy; Yasuji Matsuoka; Emmanuel Planel; Paul M Mathews
Journal:  PLoS One       Date:  2009-09-22       Impact factor: 3.240

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