The regulation of microtubule dynamics is attributed to microtubule-associated proteins that bind to the microtubule outer surface, but little is known about cellular components that may associate with the internal side of microtubules. We used cryoelectron tomography to investigate in a quantitative manner the three dimensional structure of microtubules in intact mammalian cells. We show that the lumen of microtubules in this native state is filled with discrete, globular particles with a diameter of 7 nm and spacings between 8 and 20 nm in neuronal cells. Cross-sectional views of microtubules confirm the presence of luminal material in vitreous sections of brain tissue. Most of the luminal particles had connections to the microtubule wall, as revealed in tomograms. A higher accumulation of particles was seen near the retracting plus ends of microtubules. The luminal particles were abundant in neurons, but were also observed in other cells, such as astrocytes and stem cells.
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11 September 2006
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September 05 2006
Luminal particles within cellular microtubules
Boyan K. Garvalov,
Boyan K. Garvalov
1Axonal Growth and Regeneration Group, Max Planck Institute of Neurobiology, 82152 Martinsried, Germany
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Benoît Zuber,
Benoît Zuber
2Laboratory for Ultrastructural Analysis, University of Lausanne, CH-1015 Lausanne, Switzerland
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Cédric Bouchet-Marquis,
Cédric Bouchet-Marquis
2Laboratory for Ultrastructural Analysis, University of Lausanne, CH-1015 Lausanne, Switzerland
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Mikhail Kudryashev,
Mikhail Kudryashev
3Department of Parasitology, Hygiene Institute, Heidelberg University School of Medicine, 69120 Heidelberg, Germany
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Manuela Gruska,
Manuela Gruska
4Department of Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany
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Martin Beck,
Martin Beck
4Department of Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany
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Andrew Leis,
Andrew Leis
4Department of Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany
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Friedrich Frischknecht,
Friedrich Frischknecht
3Department of Parasitology, Hygiene Institute, Heidelberg University School of Medicine, 69120 Heidelberg, Germany
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Frank Bradke,
Frank Bradke
1Axonal Growth and Regeneration Group, Max Planck Institute of Neurobiology, 82152 Martinsried, Germany
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Wolfgang Baumeister,
Wolfgang Baumeister
4Department of Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany
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Jacques Dubochet,
Jacques Dubochet
2Laboratory for Ultrastructural Analysis, University of Lausanne, CH-1015 Lausanne, Switzerland
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Marek Cyrklaff
Marek Cyrklaff
4Department of Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany
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Boyan K. Garvalov
1Axonal Growth and Regeneration Group, Max Planck Institute of Neurobiology, 82152 Martinsried, Germany
Benoît Zuber
2Laboratory for Ultrastructural Analysis, University of Lausanne, CH-1015 Lausanne, Switzerland
Cédric Bouchet-Marquis
2Laboratory for Ultrastructural Analysis, University of Lausanne, CH-1015 Lausanne, Switzerland
Mikhail Kudryashev
3Department of Parasitology, Hygiene Institute, Heidelberg University School of Medicine, 69120 Heidelberg, Germany
Manuela Gruska
4Department of Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany
Martin Beck
4Department of Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany
Andrew Leis
4Department of Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany
Friedrich Frischknecht
3Department of Parasitology, Hygiene Institute, Heidelberg University School of Medicine, 69120 Heidelberg, Germany
Frank Bradke
1Axonal Growth and Regeneration Group, Max Planck Institute of Neurobiology, 82152 Martinsried, Germany
Wolfgang Baumeister
4Department of Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany
Jacques Dubochet
2Laboratory for Ultrastructural Analysis, University of Lausanne, CH-1015 Lausanne, Switzerland
Marek Cyrklaff
4Department of Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany
Correspondence to Marek Cyrklaff: [email protected]
B. Zuber and C. Bouchet-Marquis contributed equally to this paper.
Abbreviations used in this paper: CCD, charged-couple device; CEMOVIS, cryoelectron microscopy of vitreous sections; cryo-ET, cryoelectron tomography; CTF, contrast transfer function; MAP, microtubule-associated protein.
Received:
June 14 2006
Accepted:
August 08 2006
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2006
J Cell Biol (2006) 174 (6): 759–765.
Article history
Received:
June 14 2006
Accepted:
August 08 2006
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Citation
Boyan K. Garvalov, Benoît Zuber, Cédric Bouchet-Marquis, Mikhail Kudryashev, Manuela Gruska, Martin Beck, Andrew Leis, Friedrich Frischknecht, Frank Bradke, Wolfgang Baumeister, Jacques Dubochet, Marek Cyrklaff; Luminal particles within cellular microtubules . J Cell Biol 11 September 2006; 174 (6): 759–765. doi: https://doi.org/10.1083/jcb.200606074
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