Stathmin 1/2-triggered microtubule loss mediates Golgi fragmentation in mutant SOD1 motor neurons

被引:0
作者
Sarah Bellouze
Gilbert Baillat
Dorothée Buttigieg
Pierre de la Grange
Catherine Rabouille
Georg Haase
机构
[1] Institut de Neurosciences de la Timone,Department of Cell Biology
[2] UMR 7289,undefined
[3] Centre National de la Recherche Scientifique (CNRS) and Aix-Marseille Université,undefined
[4] GenoSplice technology,undefined
[5] iPEPS - ICM,undefined
[6] Hôpital Pitié Salpêtrière,undefined
[7] Hubrecht Institute of the KNAW & UMC Utrecht,undefined
来源
Molecular Neurodegeneration | / 11卷
关键词
Amyotrophic Lateral Sclerosis; Motor Neuron; Spinal Muscular Atrophy; Mutant SOD1; SOD1G93A Mouse;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [41] Calcium-influx increases SOD1 aggregates via nitric oxide in cultured motor neurons
    Kim, Hyun-Jung
    Im, Wooseok
    Kim, Seungchan
    Kim, Sung Hun
    Sung, Jung-Jun
    Kim, Manho
    Lee, Kwang-Woo
    EXPERIMENTAL AND MOLECULAR MEDICINE, 2007, 39 (05) : 574 - 582
  • [42] Calcium-influx increases SOD1 aggregates via nitric oxide in cultured motor neurons
    Hyun-Jung Kim
    Wooseok Im
    Seungchan Kim
    Sung Hun Kim
    Jung-Jun Sung
    Manho Kim
    Kwang-Woo Lee
    Experimental & Molecular Medicine, 2007, 39 : 574 - 582
  • [43] Presymptomatic motor neuron loss and reactive astrocytosis in the sod1 mouse model of amyotrophic lateral sclerosis
    Feeney, SJ
    McKelvie, PA
    Austin, L
    Jean-Francois, MJB
    Kapsa, R
    Tombs, SM
    Byrne, E
    MUSCLE & NERVE, 2001, 24 (11) : 1510 - 1519
  • [44] DNA damage accumulates and responses are engaged in human ALS brain and spinal motor neurons and DNA repair is activatable in iPSC-derived motor neurons with SOD1 mutations
    Kim, Byung Woo
    Jeong, Ye Eun
    Wong, Margaret
    Martin, Lee J.
    ACTA NEUROPATHOLOGICA COMMUNICATIONS, 2020, 8 (01)
  • [45] Marked synergism between mutant SOD1 and glutamate transport inhibition in the induction of motor neuronal degeneration in spinal cord slice cultures
    Yin, Hong Z.
    Weiss, John H.
    BRAIN RESEARCH, 2012, 1448 : 153 - 162
  • [46] Repetitive nerve stimulation transiently opens the mitochondrial permeability transition pore in motor nerve terminals of symptomatic mutant SOD1 mice
    Nguyen, Khanh T.
    Barrett, John N.
    Garcia-Chacon, Luis
    David, Gavriel
    Barrett, Ellen F.
    NEUROBIOLOGY OF DISEASE, 2011, 42 (03) : 381 - 390
  • [47] Sertoli cells improve survival of motor neurons in SOD1 transgenic mice, a model of amyotrophic lateral sclerosis
    Hemendinger, R
    Wang, J
    Malik, S
    Persinski, R
    Copeland, J
    Emerich, D
    Gores, P
    Halberstadt, C
    Rosenfeld, J
    EXPERIMENTAL NEUROLOGY, 2005, 196 (02) : 235 - 243
  • [48] Neuronal overexpression of IP3 receptor 2 is detrimental in mutant SOD1 mice
    Staats, Kim A.
    Bogaert, Elke
    Hersmus, Nicole
    Jaspers, Tom
    Luyten, Tomas
    Bultynck, Geert
    Parys, Jan B.
    Hisatsune, Chihiro
    Mikoshiba, Katsuhiko
    Van Damme, Philip
    Robberecht, Wim
    Van den Bosch, Ludo
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2012, 429 (3-4) : 210 - 213
  • [49] RNA-Seq Profiling of Spinal Cord Motor Neurons from a Presymptomatic SOD1 ALS Mouse
    Bandyopadhyay, Urmi
    Cotney, Justin
    Nagy, Maria
    Oh, Sunghee
    Leng, Jing
    Mahajan, Milind
    Mane, Shrikant
    Fenton, Wayne A.
    Noonan, James P.
    Horwich, Arthur L.
    PLOS ONE, 2013, 8 (01):
  • [50] Mutant SOD1 prevents normal functional recovery through enhanced glial activation and loss of motor neuron innervation after peripheral nerve injury
    Schram, Sarah
    Chuang, Donald
    Schmidt, Greg
    Piponov, Hristo
    Helder, Cory
    Kerns, James
    Gonzalez, Mark
    Song, Fei
    Loeb, Jeffrey A.
    NEUROBIOLOGY OF DISEASE, 2019, 124 : 469 - 478