Literature DB >> 2061715

Neurofilament distribution is altered in the Mnd (motor neuron degeneration) mouse.

L M Callahan1, E L Wylen, A Messer, J E Mazurkiewicz.   

Abstract

Motor neuron degeneration (Mnd) is a genetic neurodegenerative disease of the mouse that is characterized by a progressive increase in motor dysfunction, moving from hind to fore limbs, leading to paralysis. An immunocytochemical analysis of the neurofilament distribution in spinal motor neurons in Mnd mice from all stages of the disease, including the presymptomatic, was performed using antibodies to different neurofilament subunits with different degrees of phosphorylation. Perikarya that stained with antibodies to phosphorylated neurofilaments were present in Mnd and control spinal cords, but the number of stained perikarya in Mnd was not significantly different from controls. There was a marked redistribution of neurofilaments within the cytoplasm of some motor neurons in Mnd cords. In Mnd but not controls, the immunoreaction product appeared marginated, leaving areas in the cytoplasm absent of immunostaining. These areas were observed in all stages of the disease, but less predictably in presymptomatics. Both the size of the areas and the number of motoneurons containing these areas appeared to increase with the severity of the disease. The number of anterior horn neurons in the hind limb region of lamina IX in spinal segment L4 of Mnd was lower than in controls, suggesting there is a loss of neurons in Mnd.

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Year:  1991        PMID: 2061715     DOI: 10.1097/00005072-199107000-00009

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  6 in total

1.  Alteration of enzymatic activities implicating neuronal degeneration in the spinal cord of the motor neuron degeneration mouse during postnatal development.

Authors:  K Fujita; K Shibayama; M Yamauchi; T Kato; M Ando; H Takahashi; K Iritani; N Yoshimoto; Y Nagata
Journal:  Neurochem Res       Date:  1998-04       Impact factor: 3.996

2.  Accumulation of the adenosine triphosphate synthase subunit C in the mnd mutant mouse. A model for neuronal ceroid lipofuscinosis.

Authors:  C A Pardo; B A Rabin; D N Palmer; D L Price
Journal:  Am J Pathol       Date:  1994-04       Impact factor: 4.307

Review 3.  The wobbler mouse: a neurodegeneration jigsaw puzzle.

Authors:  Séverine Boillée; Marc Peschanski; Marie-Pierre Junier
Journal:  Mol Neurobiol       Date:  2003-08       Impact factor: 5.590

4.  Effect of nerve growth factor on delayed neuronal death after cerebral ischaemia.

Authors:  K Tanaka; T Tsukahara; N Hashimoto; N Ogata; Y Yonekawa; T Kimura; T Taniguchi
Journal:  Acta Neurochir (Wien)       Date:  1994       Impact factor: 2.216

Review 5.  Progress in the Development of Small Molecule Therapeutics for the Treatment of Neuronal Ceroid Lipofuscinoses (NCLs).

Authors:  Nihar Kinarivala; Paul C Trippier
Journal:  J Med Chem       Date:  2015-11-24       Impact factor: 7.446

6.  The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy.

Authors:  Liina Lonka; Antti Aalto; Outi Kopra; Mervi Kuronen; Zaal Kokaia; Mart Saarma; Anna-Elina Lehesjoki
Journal:  BMC Neurosci       Date:  2005-04-13       Impact factor: 3.288

  6 in total

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