Regenerated Synapses in Lamprey Spinal Cord Are Sparse and Small Even After Functional Recovery From Injury

被引:45
|
作者
Oliphint, Paul A. [1 ]
Alieva, Naila [1 ]
Foldes, Andrea E. [1 ]
Tytell, Eric D. [2 ]
Lau, Billy Y. -B. [1 ]
Pariseau, Jenna S. [3 ]
Cohen, Avis H. [2 ]
Morgan, Jennifer R. [1 ]
机构
[1] Univ Texas Austin, Sect Mol Cell & Dev Biol, Inst Cell & Mol Biol, Inst Neurosci, Austin, TX 78712 USA
[2] Univ Maryland, Syst Res Inst, Dept Biol, Program Neurosci & Cognit Sci, College Pk, MD 20742 USA
[3] Bowdoin Coll, Dept Biol, Brunswick, ME 04011 USA
关键词
actin; active zone; axon; synaptic vesicle; ultrastructure; CENTRAL-NERVOUS-SYSTEM; LARVAL SEA LAMPREY; RETICULOSPINAL NEURONS; NEUROTRANSMITTER RELEASE; LOCOMOTOR RECOVERY; SYNAPTIC REGENERATION; AXONAL REGENERATION; TRANSECTED LAMPREY; TIME-COURSE; NEUROMUSCULAR-JUNCTION;
D O I
10.1002/cne.22368
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Despite the potential importance that synapse regeneration plays in restoring neuronal function after spinal cord injury (SCI), even the most basic questions about the morphology of regenerated synapses remain unanswered. Therefore, we set out to gain a better understanding of central synapse regeneration by examining the number, distribution, molecular composition, and ultrastructure of regenerated synapses under conditions in which behavioral recovery from SCI was robust. To do so, we used the giant reticulospinal (RS) neurons of lamprey spinal cord because they readily regenerate, are easily identifiable, and contain large synapses that serve as a classic model for vertebrate excitatory neurotransmission. Using a combination of light and electron microscopy, we found that regenerated giant RS synapses regained the basic structures and presynaptic organization observed at control giant RS synapses at a time when behavioral recovery was nearly complete. However, several obvious differences remained. Most strikingly, regenerated giant RS axons produced very few synapses. In addition, presynaptic sites within regenerated axons were less complex, had fewer vesicles, and had smaller active zones than normal. In contrast, the densities of presynapses and docked vesicles were nearly restored to control values. Thus, robust functional recovery from SCI can occur even when the structures of regenerated synapses are sparse and small, suggesting that functional recovery is due to a more complex set of compensatory changes throughout the spinal network. J. Comp. Neurol. 518:2854-2872, 2010. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:2854 / 2872
页数:19
相关论文
共 50 条
  • [21] PACAP Stimulates Functional Recovery after Spinal Cord Injury through Axonal Regeneration
    Masashi Tsuchida
    Tomoya Nakamachi
    Kouichi Sugiyama
    Daisuke Tsuchikawa
    Jun Watanabe
    Motohide Hori
    Akira Yoshikawa
    Nori Imai
    Nobuyuki Kagami
    Attila Matkovits
    Takashi Atsumi
    Seiji Shioda
    Journal of Molecular Neuroscience, 2014, 54 : 380 - 387
  • [22] BMP inhibition enhances axonal growth and functional recovery after spinal cord injury
    Matsuura, Iichiro
    Taniguchi, Junko
    Hata, Katsuhiko
    Saeki, Naokatsu
    Yamashita, Toshihide
    JOURNAL OF NEUROCHEMISTRY, 2008, 105 (04) : 1471 - 1479
  • [23] Highly conserved molecular pathways, including Wnt signaling, promote functional recovery from spinal cord injury in lampreys
    Herman, Paige E.
    Papatheodorou, Angelos
    Bryant, Stephanie A.
    Waterbury, Courtney K. M.
    Herdy, Joseph R.
    Arcese, Anthony A.
    Buxbaum, Joseph D.
    Smith, Jeramiah J.
    Morgan, Jennifer R.
    Bloom, Ona
    SCIENTIFIC REPORTS, 2018, 8
  • [24] Activated Erk Is an Early Retrograde Signal After Spinal Cord Injury in the Lamprey
    Jin, Li-Qing
    John, Brittany H.
    Hu, Jianli
    Selzer, Michael E.
    FRONTIERS IN NEUROSCIENCE, 2020, 14
  • [25] PACAP Stimulates Functional Recovery after Spinal Cord Injury through Axonal Regeneration
    Tsuchida, Masashi
    Nakamachi, Tomoya
    Sugiyama, Kouichi
    Tsuchikawa, Daisuke
    Watanabe, Jun
    Hori, Motohide
    Yoshikawa, Akira
    Imai, Nori
    Kagami, Nobuyuki
    Matkovits, Attila
    Atsumi, Takashi
    Shioda, Seiji
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2014, 54 (03) : 380 - 387
  • [26] The role of the serotonergic system in locornotor recovery after spinal cord injury
    Ghosh, Mousumi
    Pearse, Damien D.
    FRONTIERS IN NEURAL CIRCUITS, 2015, 8
  • [27] The role of propriospinal interneurons in recovery from spinal cord injury
    Flynn, Jamie R.
    Graham, Brett A.
    Galea, Mary P.
    Callister, Robert J.
    NEUROPHARMACOLOGY, 2011, 60 (05) : 809 - 822
  • [28] Lentiviral Delivery of miR-133b Improves Functional Recovery After Spinal Cord Injury in Mice
    Theis, Thomas
    Yoo, Myung
    Park, Christopher S.
    Chen, Jian
    Kuegler, Sebastian
    Gibbs, Kurt M.
    Schachner, Melitta
    MOLECULAR NEUROBIOLOGY, 2017, 54 (06) : 4659 - 4671
  • [29] Cotransplantation of Glial Restricted Precursor Cells and Schwann Cells Promotes Functional Recovery After Spinal Cord Injury
    Hu, Jian-Guo
    Wang, Xiao-Fei
    Deng, Ling-Xiao
    Liu, Nai-Kui
    Gao, Xiang
    Chen, Jing-Hui
    Zhou, Feng-Cheng
    Xu, Xiao-Ming
    CELL TRANSPLANTATION, 2013, 22 (12) : 2219 - 2236
  • [30] Inhibition of neogenin promotes neuronal survival and improved behavior recovery after spinal cord injury
    Chen, Jie
    Shifman, Michael, I
    NEUROSCIENCE, 2019, 408 : 430 - 447