In vivo imaging of axonal degeneration and regeneration in the injured spinal cord

被引:444
作者
Kerschensteiner, M
Schwab, ME
Lichtman, JW
Misgeld, T
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] ETH, Dept Biol, Brain Res Inst, Dept Neuromorphol, CH-8057 Zurich, Switzerland
[3] Univ Zurich, CH-8057 Zurich, Switzerland
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nm1229
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The poor response of central axons to transection underlies the bleak prognosis following spinal cord injury. Here, we monitor individual fluorescent axons in the spinal cords of living transgenic mice over several days after spinal injury. We find that within 30 min after trauma, axons die back hundreds of micrometers. This acute form of axonal degeneration is similar in mechanism to the more delayed Wallerian degeneration of the disconnected distal axon, but acute degeneration affects the proximal and distal axon ends equally. In vivo imaging further shows that many axons attempt regeneration within 6-24 h after lesion. This growth response, although robust, seems to fail as a result of the inability of axons to navigate in the proper direction. These results suggest that time-lapse imaging of spinal cord injury may provide a powerful analytical tool for assessing the pathogenesis of spinal cord injury and for evaluating therapies that enhance regeneration.
引用
收藏
页码:572 / 577
页数:6
相关论文
共 23 条
  • [1] The injured spinal cord spontaneously forms a new intraspinal circuit in adult rats
    Bareyre, FM
    Kerschensteiner, M
    Raineteau, O
    Mettenleiter, TC
    Weinmann, O
    Schwab, ME
    [J]. NATURE NEUROSCIENCE, 2004, 7 (03) : 269 - 277
  • [2] Quantitative and qualitative analysis of Wallerian degeneration using restricted axonal labelling in YFP-H mice
    Beirowski, B
    Berek, L
    Adalbert, R
    Wagner, D
    Grumme, DS
    Addicks, K
    Ribchester, RR
    Coleman, MP
    [J]. JOURNAL OF NEUROSCIENCE METHODS, 2004, 134 (01) : 23 - 35
  • [3] CAJAL SRY, 1991, DEGENERATION REGENER, pCH4
  • [4] Neutralization of CD95 ligand promotes regeneration and functional recovery after spinal cord injury
    Demjen, D
    Klussmann, S
    Kleber, S
    Zuliani, C
    Stieltjes, B
    Metzger, C
    Hirt, UA
    Walczak, H
    Falk, W
    Essig, M
    Edler, L
    Krammer, PH
    Martin-Villalba, A
    [J]. NATURE MEDICINE, 2004, 10 (04) : 389 - 395
  • [5] Imaging neuronal subsets in transgenic mice expressing multiple spectral variants of GFP
    Feng, GP
    Mellor, RH
    Bernstein, M
    Keller-Peck, C
    Nguyen, QT
    Wallace, M
    Nerbonne, JM
    Lichtman, JW
    Sanes, JR
    [J]. NEURON, 2000, 28 (01) : 41 - 51
  • [6] CORTICOSPINAL TRACT PLASTICITY AND ASTROGLIAL REACTIVITY AFTER CERVICAL SPINAL-INJURY IN THE POSTNATAL RAT
    FIRKINS, SS
    BATES, CA
    STELZNER, DJ
    [J]. EXPERIMENTAL NEUROLOGY, 1993, 120 (01) : 1 - 15
  • [7] GEORGE EB, 1995, J NEUROSCI, V15, P6445
  • [8] Age-dependent synapse withdrawal at axotomised neuromuscular junctions in Wlds mutant and Ube4b/Nmnat transgenic mice
    Gillingwater, TH
    Thomson, D
    Mack, TGA
    Soffin, EM
    Mattison, RJ
    Coleman, MP
    Ribchester, RR
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 2002, 543 (03): : 739 - 755
  • [9] Degeneration and sprouting of identified descending supraspinal axons after contusive spinal cord injury in the rat
    Hill, CE
    Beattie, MS
    Bresnahan, JC
    [J]. EXPERIMENTAL NEUROLOGY, 2001, 171 (01) : 153 - 169
  • [10] Chronically injured supraspinal neurons exhibit only modest axonal dieback in response to a cervical hemisection lesion
    Houle, JD
    Jin, Y
    [J]. EXPERIMENTAL NEUROLOGY, 2001, 169 (01) : 208 - 217