Literature DB >> 11085877

Intracellular distribution of myelin protein gene products is altered in oligodendrocytes of the taiep rat.

L T O'Connor1, B D Goetz, E Couve, J Song, I D Duncan.   

Abstract

Hypomyelination and subsequent demyelination of the taiep rat CNS are thought to result from the abnormal accumulation of microtubules (MTs) in oligodendrocytes that disrupts intracellular transport of components needed to form and maintain the myelin sheath. In this study, myelin gene expression was evaluated in mutant and age-matched controls to determine if MT abnormalities affect the distribution of myelin proteins and their mRNAs. Immunohistochemical analysis of taiep brains and spinal cords revealed a gradual decrease in levels of several myelin proteins including myelin basic protein (MBP), proteolipid protein (PLP), myelin-associated glycoprotein (MAG), and 2',3'-cyclic nucleotide 3'-phosphodiesterase. Accompanying early declines in MAG and PLP, accumulations of immunoreactive products were detected within oligodendrocytes, consistent with a defect in protein trafficking. Northern blot analysis indicated that diminishing protein levels could not be attributed to changes in transcriptional activity, except for MBP of which mRNA levels decreased with age. Cellular localization of MBP mRNA by in situ hybridization further revealed that transcripts were concentrated within oligodendrocyte cell bodies instead of uniformly distributed throughout processes. These results demonstrate that changes in expression and intracellular localization of myelin gene products are concurrent with increases in MT mass in taiep oligodendrocytes and support our hypothesis that cytoskeletal defects prevent the normal transport of elements required for the formation and maintenance of the myelin sheath.

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Year:  2000        PMID: 11085877     DOI: 10.1006/mcne.2000.0889

Source DB:  PubMed          Journal:  Mol Cell Neurosci        ISSN: 1044-7431            Impact factor:   4.314


  9 in total

1.  Conditional knockout of TOG results in CNS hypomyelination.

Authors:  Michael J Maggipinto; Joshay Ford; Kristine H Le; Jessica W Tutolo; Miki Furusho; John W Wizeman; Rashmi Bansal; Elisa Barbarese
Journal:  Glia       Date:  2017-01-07       Impact factor: 7.452

Review 2.  The myelin mutants as models to study myelin repair in the leukodystrophies.

Authors:  Ian D Duncan; Yoichi Kondo; Su-Chun Zhang
Journal:  Neurotherapeutics       Date:  2011-10       Impact factor: 7.620

3.  A mutation in the Tubb4a gene leads to microtubule accumulation with hypomyelination and demyelination.

Authors:  Ian D Duncan; Marianna Bugiani; Abigail B Radcliff; John J Moran; Camila Lopez-Anido; Phu Duong; Benjamin K August; Nicole I Wolf; Marjo S van der Knaap; John Svaren
Journal:  Ann Neurol       Date:  2017-05-09       Impact factor: 10.422

4.  A mutation in the canine gene encoding folliculin-interacting protein 2 (FNIP2) associated with a unique disruption in spinal cord myelination.

Authors:  Trevor J Pemberton; Sunju Choi; Joshua A Mayer; Fang-Yuan Li; Nolan Gokey; John Svaren; Noa Safra; Danika L Bannasch; Katrina Sullivan; Babetta Breuhaus; Pragna I Patel; Ian D Duncan
Journal:  Glia       Date:  2014-01       Impact factor: 7.452

5.  The transcriptome of mouse central nervous system myelin.

Authors:  Sudhir Thakurela; Angela Garding; Ramona B Jung; Christina Müller; Sandra Goebbels; Robin White; Hauke B Werner; Vijay K Tiwari
Journal:  Sci Rep       Date:  2016-05-13       Impact factor: 4.379

6.  Impact of simulated microgravity on oligodendrocyte development: implications for central nervous system repair.

Authors:  Araceli Espinosa-Jeffrey; Pablo M Paez; Veronica T Cheli; Vilma Spreuer; Ina Wanner; Jean de Vellis
Journal:  PLoS One       Date:  2013-12-04       Impact factor: 3.240

Review 7.  Inherited and acquired disorders of myelin: The underlying myelin pathology.

Authors:  Ian D Duncan; Abigail B Radcliff
Journal:  Exp Neurol       Date:  2016-04-09       Impact factor: 5.330

8.  Neural stem cells restore myelin in a demyelinating model of Pelizaeus-Merzbacher disease.

Authors:  Fredrik I Gruenenfelder; Mark McLaughlin; Ian R Griffiths; James Garbern; Gemma Thomson; Peter Kuzman; Jennifer A Barrie; Maj-Lis McCulloch; Jacques Penderis; Ruth Stassart; Klaus-Armin Nave; Julia M Edgar
Journal:  Brain       Date:  2020-05-01       Impact factor: 13.501

9.  TUBB4A mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse model.

Authors:  Sunetra Sase; Akshata A Almad; C Alexander Boecker; Pedro Guedes-Dias; Jian J Li; Asako Takanohashi; Akshilkumar Patel; Tara McCaffrey; Heta Patel; Divya Sirdeshpande; Julian Curiel; Judy Shih-Hwa Liu; Quasar Padiath; Erika Lf Holzbaur; Steven S Scherer; Adeline Vanderver
Journal:  Elife       Date:  2020-05-28       Impact factor: 8.713

  9 in total

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