Quantification of motor neuron loss and muscular atrophy in ricin-induced focal nerve injury

被引:7
|
作者
Liang, Yajie [1 ,2 ,3 ]
Zhang, Jiangyang [1 ]
Walczak, Piotr [1 ,2 ,3 ,7 ]
Bulte, Jeff W. M. [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Johns Hopkins Univ, Sch Med, Div MR Res, Russell H Morgan Dept Radiol & Radiol Sci, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Cellular Imaging Sect, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Vasc Biol Program, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Whiting Sch Engn, Dept Chem & Biomol Engn, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
[7] Univ Warmia & Mazury, Fac Med Sci, Dept Neurol & Neurosurg, Olsztyn, Poland
关键词
Motor neuron; Ricin; Sciatic nerve; Magnetic resonance imaging; Muscle atrophy; Neuronal tracing; CATWALK GAIT ANALYSIS; STEM-CELLS; RAT MODEL; A-CHAIN; TRANSPLANTATION; DEGENERATION; MICE; MOTONEURONS; EXPRESSION; INJECTION;
D O I
10.1016/j.jneumeth.2018.07.014
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Intrasciatic nerve injection of the Ricinus communis agglutinin (RCA or ricin) causes degeneration of motor neurons (MNs) with functional deficits, such as those that occur in amyotrophic lateral sclerosis (ALS). The objective of this study was to develop a new comprehensive platform for quantitative evaluation of MN loss, muscular atrophy and behavioral deficits using different ricin injection regimens. New method: Fluorogold (FG)-guided stereological quantification of MNs, in vivo magnetic resonance imaging (MRI) of muscular atrophy, and CatWalk behavioral testing were used to evaluate the outcome of rats treated with different ricin regimens (RCA60 0.5 mu g, RCA60 3 mu g, and RCA120 6 mu g) as animal models of MN degeneration. Results: FG-guided stereological counting of MNs enabled identification, dissection and robust quantification of ricin-induced MN loss. The RCA60 0.5 mu g and RCA120 6 mu g regimens were found to be best suited as preclinical MN depletion models, with a low mortality and a reproducible MN loss, accompanied by muscle atrophy and functional deficits evaluated by MRI and the CatWalk method, respectively. Comparison with existing methods: 1) Fluorogold neuronal tracing provides a robust and straightforward means for quantifying MN loss in the spinal cord; 2) MRI is well-suited to non-invasively assess muscle atrophy; and 3) The CatWalk method is more flexible than rotarod test for studying motor deficits. Conclusion: Intrasciatic injection of RCA60 or RCA120 induces nerve injury and muscle atrophy, which can be properly evaluated by a comprehensive platform using FG-guided quantitative 3D topographic histological analysis, MRI and the CatWalk behavioral test.
引用
收藏
页码:142 / 150
页数:9
相关论文
共 50 条
  • [41] Deletions in the Survival Motor Neuron Gene in Iranian Patients with Spinal Muscular Atrophy
    Hasanzad, Mandana
    Golkar, Zahra
    Kariminejad, Roxana
    Hadavi, Valeh
    Almadani, Navid
    Afroozan, Fariba
    Salahshurifar, Iman
    Shafeghati, Yousef
    Kahrizi, Kimia
    Najmabadi, Hossein
    ANNALS ACADEMY OF MEDICINE SINGAPORE, 2009, 38 (02) : 139 - 141
  • [42] Hybrid survival motor neuron genes in Japanese patients with spinal muscular atrophy
    Nishio, H
    Horikawa, H
    Yakura, H
    Sugie, K
    Nakamuro, T
    Koterazawa, K
    Ishikawa, Y
    Lee, MJ
    Wada, H
    Takeshima, Y
    Matsuo, M
    Sumino, K
    ACTA NEUROLOGICA SCANDINAVICA, 1999, 99 (06): : 374 - 380
  • [43] Copies of the survival motor neuron gene in spinal muscular atrophy: the more, the better
    Brahe, C
    NEUROMUSCULAR DISORDERS, 2000, 10 (4-5) : 274 - 275
  • [44] Spinal Muscular Atrophy and the Antiapoptotic Role of Survival of Motor Neuron (SMN) Protein
    Ryan S. Anderton
    Bruno P. Meloni
    Frank L. Mastaglia
    Sherif Boulos
    Molecular Neurobiology, 2013, 47 : 821 - 832
  • [45] Inherited Motor Neuron Disease in Domestic Cats: A Model of Spinal Muscular Atrophy
    Qianchuan He
    Charles Lowrie
    G Diane Shelton
    Rudy J Castellani
    Marilyn Menotti-Raymond
    William Murphy
    Stephen J O'Brien
    William F Swanson
    John C Fyfe
    Pediatric Research, 2005, 57 : 324 - 330
  • [47] Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy
    Zhang, Zhenxi
    Pinto, Anna Maria
    Wan, Lili
    Wang, Wei
    Berg, Michael G.
    Oliva, Isabela
    Singh, Larry N.
    Dengler, Christopher
    Wei, Zhi
    Dreyfuss, Gideon
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (48) : 19348 - 19353
  • [48] Spinal muscular atrophy: a motor neuron disorder or a multi-organ disease?
    Shababi, Monir
    Lorson, Christian L.
    Rudnik-Schoeneborn, Sabine S.
    JOURNAL OF ANATOMY, 2014, 224 (01) : 15 - 28
  • [49] Genetic circuitry of Survival motor neuron, the gene underlying spinal muscular atrophy
    Sen, Anindya
    Dimlich, Douglas N.
    Guruharsha, K. G.
    Kankel, Mark W.
    Hori, Kazuya
    Yokokura, Takakazu
    Brachat, Sophie
    Richardson, Delwood
    Loureiro, Joseph
    Sivasankaran, Rajeev
    Curtis, Daniel
    Davidow, Lance S.
    Rubin, Lee L.
    Hart, Anne C.
    Van Vactor, David
    Artavanis-Tsakonas, Spyros
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (26) : E2371 - E2380
  • [50] Other forms of survival motor neuron protein and spinal muscular atrophy: An opinion
    Burghes, H. M.
    NEUROMUSCULAR DISORDERS, 2008, 18 (01) : 82 - 83