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学術論文

Three-dimensional imaging of the unsectioned adult spinal cord to assess axon regeneration and glial responses after injury

MPS-Authors
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Ertürk,  Ali
Max Planck Research Group: Axonal Growth and Regeneration / Bradke, MPI of Neurobiology, Max Planck Society;

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Hellal,  Farida
Max Planck Research Group: Axonal Growth and Regeneration / Bradke, MPI of Neurobiology, Max Planck Society;

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Förstner,  Friedrich
Department: Systems and Computational Neurobiology / Borst, MPI of Neurobiology, Max Planck Society;

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Keck,  Tara
Department: Cellular and Systems Neurobiology / Bonhoeffer, MPI of Neurobiology, Max Planck Society;

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Hübener,  Mark
Department: Cellular and Systems Neurobiology / Bonhoeffer, MPI of Neurobiology, Max Planck Society;

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Bradke,  Frank
Max Planck Research Group: Axonal Growth and Regeneration / Bradke, MPI of Neurobiology, Max Planck Society;

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引用

Ertürk, A., Mauch, C. P., Hellal, F., Förstner, F., Keck, T., Becker, K., Jaehrling, N., Steffens, H., Richter, M., Hübener, M., Kramer, E., Kirchhoff, F., Dodt, H. U., & Bradke, F. (2012). Three-dimensional imaging of the unsectioned adult spinal cord to assess axon regeneration and glial responses after injury. Nature Medicine, 18(1), 166-171. doi:10.1038/nm.2600.


引用: https://hdl.handle.net/11858/00-001M-0000-000F-41B3-8
要旨
Studying regeneration in the central nervous system (CNS) is hampered
by current histological and imaging techniques because they provide
only partial information about axonal and glial reactions. Here we
developed a tetrahydrofuranbased clearing procedure that renders fixed
and unsectioned adult CNS tissue transparent and fully penetrable for
optical imaging. In large spinal cord segments, we imaged fluorescently
labeled cells by `ultramicroscopy' and two-photon microscopy without
the need for histological sectioning. We found that more than a year
after injury growth-competent axons regenerated abundantly through the
injury site. A few growth-incompetent axons could also regenerate when
they bypassed the lesion. Moreover, we accurately determined
quantitative changes of glial cells after spinal cord injury. Thus,
clearing CNS tissue enables an unambiguous evaluation of axon
regeneration and glial reactions. Our clearing procedure also renders
other organs transparent, which makes this approach useful for a large
number of preclinical paradigms.