Literature DB >> 11033335

Motor neuron disease in vitro: the use of cultured motor neurons to study amyotrophic lateral sclerosis.

P R Bär1.   

Abstract

Amyotrophic lateral sclerosis (ALS) is a lethal neurodegenerative disease in which motor neurons in the nervous system die. The cause is unknown, and no effective treatment exists. Mutations in the gene for superoxide dismutase found in a subpopulation have led to an animal model, but research with these mice has not produced complete insight into the disease mechanism. Studies with isolated motor neurons may produce important information. This review discusses approaches to culture motor neurons - single cells, cocultured with other cells, and in intact preparations, such as the spinal or cortical slice. Motor neurons in monoculture are suitable for acute but not for chronic studies, whereas cocultures and slices survive up to months and are used for chronic studies. Results with toxic substances believed to play a role in the disease, such as oxidants and glutamate, and of studies where the energy status of the cells is manipulated, are presented.

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Year:  2000        PMID: 11033335     DOI: 10.1016/s0014-2999(00)00560-4

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  7 in total

Review 1.  Mechanisms of neurodegeneration in amyotrophic lateral sclerosis.

Authors:  S Cluskey; D B Ramsden
Journal:  Mol Pathol       Date:  2001-12

2.  Amyotrophic lateral sclerosis: Protein chaperone dysfunction revealed by proteomic studies of animal models.

Authors:  Mohit Raja Jain; Wei-Wen Ge; Stella Elkabes; Hong Li
Journal:  Proteomics Clin Appl       Date:  2008-05-01       Impact factor: 3.494

3.  Antioxidant capacity and protein oxidation in cerebrospinal fluid of amyotrophic lateral sclerosis.

Authors:  G Siciliano; S Piazza; C Carlesi; A Del Corona; M Franzini; A Pompella; G Malvaldi; M Mancuso; A Paolicchi; L Murri
Journal:  J Neurol       Date:  2007-04-11       Impact factor: 4.849

4.  Altered Metabolic Profiles Associate with Toxicity in SOD1G93A Astrocyte-Neuron Co-Cultures.

Authors:  Gabriel N Valbuena; Massimo Tortarolo; Caterina Bendotti; Lavinia Cantoni; Hector C Keun
Journal:  Sci Rep       Date:  2017-03-03       Impact factor: 4.379

5.  RNS60 exerts therapeutic effects in the SOD1 ALS mouse model through protective glia and peripheral nerve rescue.

Authors:  Antonio Vallarola; Francesca Sironi; Massimo Tortarolo; Noemi Gatto; Roberta De Gioia; Laura Pasetto; Massimiliano De Paola; Alessandro Mariani; Supurna Ghosh; Richard Watson; Andreas Kalmes; Valentina Bonetto; Caterina Bendotti
Journal:  J Neuroinflammation       Date:  2018-03-01       Impact factor: 8.322

6.  Impairment of mitochondrial calcium handling in a mtSOD1 cell culture model of motoneuron disease.

Authors:  Manoj Kumar Jaiswal; Wolf-Dieter Zech; Miriam Goos; Christine Leutbecher; Alberto Ferri; Annette Zippelius; Maria Teresa Carrì; Roland Nau; Bernhard U Keller
Journal:  BMC Neurosci       Date:  2009-06-22       Impact factor: 3.288

7.  High yield extraction of pure spinal motor neurons, astrocytes and microglia from single embryo and adult mouse spinal cord.

Authors:  Marie-Josée Beaudet; Qiurui Yang; Sébastien Cadau; Mathieu Blais; Sabrina Bellenfant; François Gros-Louis; François Berthod
Journal:  Sci Rep       Date:  2015-11-18       Impact factor: 4.379

  7 in total

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