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
  • [21] Stasimon contributes to the loss of sensory synapses and motor neuron death in a mouse model of spinal muscular atrophy
    Simon, C. M.
    Van Alstyne, M.
    Lotti, F.
    Bianchetti, E.
    Tisdale, S.
    Mentis, G.
    Pellizzoni, L.
    ACTA PHYSIOLOGICA, 2019, 227
  • [22] A Model of Motor Neuron Loss: Selective Deficits after Ricin Injection
    Coutts, Margaret
    Kong, Ling X.
    Keirstead, Hans S.
    JOURNAL OF NEUROTRAUMA, 2010, 27 (07) : 1333 - 1342
  • [23] Motor neuron apoptosis in type 1 spinal muscular atrophy mouse
    Wang, CC
    Tsai, KB
    Jong, YJ
    FASEB JOURNAL, 2004, 18 (05): : A1184 - A1184
  • [24] PROGRESSIVE MUSCULAR ATROPHY AND OTHER LOWER MOTOR NEURON SYNDROMES OF ADULTS
    Rowland, Lewis P.
    MUSCLE & NERVE, 2010, 41 (02) : 161 - 165
  • [25] Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular Atrophy
    Teoh, Hooi Ling
    Carey, Kate
    Sampaio, Hugo
    Mowat, David
    Roscioli, Tony
    Farrar, Michelle
    NEURAL PLASTICITY, 2017, 2017
  • [26] The survival motor neuron protein (SMN) in spinal muscular atrophy (SMA).
    Coovert, DD
    Le, T
    McAndrew, PE
    Strasswimmer, J
    Crawford, TO
    Mendell, JR
    Androphy, E
    Prior, TW
    Burghes, AHM
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A329 - A329
  • [27] Overturning the Paradigm of Spinal Muscular Atrophy as Just a Motor Neuron Disease
    Yeo, Crystal Jing Jing
    Darras, Basil T.
    PEDIATRIC NEUROLOGY, 2020, 109 : 12 - 19
  • [28] Infantile spinal muscular atrophy: more than a motor neuron disease?
    Rudnik-Schoeneborn, S.
    Lorson, C. L.
    Shababi, M.
    MEDIZINISCHE GENETIK, 2013, 25 (03) : 347 - 351
  • [29] Sensory Neurons Do Not Induce Motor Neuron Loss in a Human Stem Cell Model of Spinal Muscular Atrophy
    Schwab, Andrew J.
    Ebert, Allison D.
    PLOS ONE, 2014, 9 (07):
  • [30] NERVE, NEURO-MUSCULAR JUNCTION AND MOTOR NEURON DISEASES
    Leger, Jean-Marc
    CURRENT OPINION IN NEUROLOGY, 2012, 25 (05) : 521 - 522