Author
Listed:
- Tatjana Kleele
(Institute of Neuronal Cell Biology, Technische Universität München, 80802)
- Petar Marinković
(Center for Neuropathology and Prion Research, Ludwig-Maximilians-Universität München, 81377
German Center for Neurodegenerative Diseases (DZNE), 80336)
- Philip R. Williams
(Institute of Neuronal Cell Biology, Technische Universität München, 80802)
- Sina Stern
(Axon Growth and Regeneration, German Center for Neurodegenerative Diseases (DZNE), 53175)
- Emily E. Weigand
(Indiana University School of Medicine–Muncie)
- Peter Engerer
(Institute of Neuronal Cell Biology, Technische Universität München, 80802)
- Ronald Naumann
(Transgenic Core Facility, Max-Planck-Institute of Molecular Cell Biology and Genetics, 01307)
- Jana Hartmann
(Institute of Neuroscience, Technische Universität München, 80802)
- Rosa M. Karl
(Institute of Neuroscience, Technische Universität München, 80802)
- Frank Bradke
(Axon Growth and Regeneration, German Center for Neurodegenerative Diseases (DZNE), 53175)
- Derron Bishop
(Indiana University School of Medicine–Muncie)
- Jochen Herms
(Center for Neuropathology and Prion Research, Ludwig-Maximilians-Universität München, 81377
German Center for Neurodegenerative Diseases (DZNE), 80336
Munich Cluster for Systems Neurology (SyNergy), 80336)
- Arthur Konnerth
(Institute of Neuroscience, Technische Universität München, 80802
Munich Cluster for Systems Neurology (SyNergy), 80336
Center of Integrated Protein Science (CIPSM), 81377)
- Martin Kerschensteiner
(Munich Cluster for Systems Neurology (SyNergy), 80336
Institute of Clinical Neuroimmunology, Ludwig-Maximilians Universität München, 81377)
- Leanne Godinho
(Institute of Neuronal Cell Biology, Technische Universität München, 80802)
- Thomas Misgeld
(Institute of Neuronal Cell Biology, Technische Universität München, 80802
German Center for Neurodegenerative Diseases (DZNE), 80336
Munich Cluster for Systems Neurology (SyNergy), 80336
Center of Integrated Protein Science (CIPSM), 81377)
Abstract
Microtubule dynamics in neurons play critical roles in physiology, injury and disease and determine microtubule orientation, the cell biological correlate of neurite polarization. Several microtubule binding proteins, including end-binding protein 3 (EB3), specifically bind to the growing plus tip of microtubules. In the past, fluorescently tagged end-binding proteins have revealed microtubule dynamics in vitro and in non-mammalian model organisms. Here, we devise an imaging assay based on transgenic mice expressing yellow fluorescent protein-tagged EB3 to study microtubules in intact mammalian neurites. Our approach allows measurement of microtubule dynamics in vivo and ex vivo in peripheral nervous system and central nervous system neurites under physiological conditions and after exposure to microtubule-modifying drugs. We find an increase in dynamic microtubules after injury and in neurodegenerative disease states, before axons show morphological indications of degeneration or regrowth. Thus increased microtubule dynamics might serve as a general indicator of neurite remodelling in health and disease.
Suggested Citation
Tatjana Kleele & Petar Marinković & Philip R. Williams & Sina Stern & Emily E. Weigand & Peter Engerer & Ronald Naumann & Jana Hartmann & Rosa M. Karl & Frank Bradke & Derron Bishop & Jochen Herms & A, 2014.
"An assay to image neuronal microtubule dynamics in mice,"
Nature Communications, Nature, vol. 5(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms5827
DOI: 10.1038/ncomms5827
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