A general homeostatic principle following lesion induced dendritic remodeling

被引:20
作者
Platschek, Steffen [1 ]
Cuntz, Hermann [1 ,2 ,3 ]
Vuksic, Mario [1 ,4 ]
Deller, Thomas [1 ]
Jedlicka, Peter [1 ]
机构
[1] Goethe Univ Frankfurt, Neurosci Ctr, Inst Clin Neuroanat, D-60590 Frankfurt, Germany
[2] Max Planck Gesell, Ernst Strungmann Inst ESI Neurosci Cooperat, D-60528 Frankfurt, Germany
[3] Frankfurt Inst Adv Studies, D-60438 Frankfurt, Germany
[4] Univ Zagreb, Sch Med, Croatian Inst Brain Res, HR-10000 Zagreb, Croatia
来源
ACTA NEUROPATHOLOGICA COMMUNICATIONS | 2016年 / 4卷
关键词
Electrotonic analysis; Computer simulation; Compartmental modeling; Morphological modeling; Voltage attenuation; Backpropagating action potential; Homeostatic plasticity; Granule cell; ENTORHINAL CORTEX LESION; DENTATE GRANULE CELLS; RAT FASCIA-DENTATA; SYNAPTIC INTEGRATION; DEPENDENT PLASTICITY; ACTION-POTENTIALS; PYRAMIDAL NEURON; GYRUS; MODEL; REORGANIZATION;
D O I
10.1186/s40478-016-0285-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Introduction: Neuronal death and subsequent denervation of target areas are hallmarks of many neurological disorders. Denervated neurons lose part of their dendritic tree, and are considered "atrophic", i.e. pathologically altered and damaged. The functional consequences of this phenomenon are poorly understood. Results: Using computational modelling of 3D-reconstructed granule cells we show that denervation-induced dendritic atrophy also subserves homeostatic functions: By shortening their dendritic tree, granule cells compensate for the loss of inputs by a precise adjustment of excitability. As a consequence, surviving afferents are able to activate the cells, thereby allowing information to flow again through the denervated area. In addition, action potentials backpropagating from the soma to the synapses are enhanced specifically in reorganized portions of the dendritic arbor, resulting in their increased synaptic plasticity. These two observations generalize to any given dendritic tree undergoing structural changes. Conclusions: Structural homeostatic plasticity, i.e. homeostatic dendritic remodeling, is operating in long-term denervated neurons to achieve functional homeostasis.
引用
收藏
页数:11
相关论文
共 75 条
  • [1] [Anonymous], 1964, Neural theory and modeling, DOI DOI 10.7551/MITPRESS/6743.003.0015
  • [2] [Anonymous], 1989, Methods in Neuronal Modeling
  • [3] Role of multiple calcium and calcium-dependent conductances in regulation of hippocampal dentate granule cell excitability
    Aradi, I
    Holmes, WR
    [J]. JOURNAL OF COMPUTATIONAL NEUROSCIENCE, 1999, 6 (03) : 215 - 235
  • [4] Tumor necrosis factor (TNF)-receptor 1 and 2 mediate homeostatic synaptic plasticity of denervated mouse dentate granule cells
    Becker, Denise
    Deller, Thomas
    Vlachos, Andreas
    [J]. SCIENTIFIC REPORTS, 2015, 5
  • [5] Targeted dendrotomy reveals active and passive contributions of the dendritic tree to synaptic integration and neuronal output
    Bekkers, John M.
    Haeusser, Michael
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (27) : 11447 - 11452
  • [6] The Neuropathology and Neurobiology of Traumatic Brain Injury
    Blennow, Kaj
    Hardy, John
    Zetterberg, Henrik
    [J]. NEURON, 2012, 76 (05) : 886 - 899
  • [7] Synaptic Integration Gradients in Single Cortical Pyramidal Cell Dendrites
    Branco, Tiago
    Haeusser, Michael
    [J]. NEURON, 2011, 69 (05) : 885 - 892
  • [8] Dendritic Discrimination of Temporal Input Sequences in Cortical Neurons
    Branco, Tiago
    Clark, Beverley A.
    Haeusser, Michael
    [J]. SCIENCE, 2010, 329 (5999) : 1671 - 1675
  • [9] Activity-dependent structural plasticity
    Butz, Markus
    Woergoetter, Florentin
    van Ooyen, Arjen
    [J]. BRAIN RESEARCH REVIEWS, 2009, 60 (02) : 287 - 305
  • [10] DENDRITIC REORGANIZATION IN THE DENERVATED DENTATE GYRUS OF THE RAT FOLLOWING ENTORHINAL CORTICAL-LESIONS - A GOLGI AND ELECTRON-MICROSCOPIC ANALYSIS
    CACERES, A
    STEWARD, O
    [J]. JOURNAL OF COMPARATIVE NEUROLOGY, 1983, 214 (04) : 387 - 403