Literature DB >> 19918120

Selective nuclear shrinkage of oligodendrocytes lacking glial cytoplasmic inclusions in multiple system atrophy: a 3-dimensional volumetric study.

Naoto Uyama1, Toshiki Uchihara, Yoko Mochizuki, Ayako Nakamura, Ryosuke Takahashi, Toshio Mizutani.   

Abstract

Glial cytoplasmic inclusions (GCIs) are a pathologic hallmark of multiple system atrophy (MSA), but their pathogenetic roles need to be clarified. To determine possible roles of GCIs in individual cells, serial optical sections obtained by confocal microscopy were reconstructed to yield 3-dimensional (3D) images of the nuclei to quantify nuclear volume. Oligodendroglial nuclear volumes were determined in the pons of 6 MSA and 7 control patients. The nuclear volumes were significantly smaller in the MSA group as a whole (135.81 +/- 60.83 microm, mean +/- SD; n = 404) than in the control group (188.05 +/- 55.71 microm; n = 308; p < 0.001). This difference was due to a significantly smaller nuclear volume of oligodendrocytes without GCIs (GCI group, 91.26 +/- 23.77 microm; n = 210) compared with the control group (p < 0.001) and compared with the oligodendrocytes with GCIs (GCI group, 184.03 +/- 51.18 microm; n = 194; p < 0.001); the difference between the latter GCI and control groups was not significant (p > 0.05). This selective decrease in nuclear volume restricted to the GCI group cannot be explained if nuclear shrinkage was accelerated in the presence of GCIs. Conversely, GCI formation might be linked, either directly or indirectly, to a mechanism that counteracts rather than accelerates nuclear shrinkage. This novel 3-dimensional strategy provides pivotal data that link GCI formation and degeneration in MSA.

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Year:  2009        PMID: 19918120     DOI: 10.1097/NEN.0b013e3181b67678

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


  6 in total

1.  Decreased oligodendrocyte nuclear diameter in Alzheimer's disease and Lewy body dementia.

Authors:  Eva Gagyi; Bernadett Kormos; Karla J Castellanos; Klara Valyi-Nagy; Dennis Korneff; Patrizia LoPresti; Randy Woltjer; Tibor Valyi-Nagy
Journal:  Brain Pathol       Date:  2012-04-12       Impact factor: 6.508

2.  α-Synuclein-induced myelination deficit defines a novel interventional target for multiple system atrophy.

Authors:  Benjamin Ettle; Bilal E Kerman; Elvira Valera; Clarissa Gillmann; Johannes C M Schlachetzki; Simone Reiprich; Christian Büttner; Arif B Ekici; André Reis; Michael Wegner; Tobias Bäuerle; Markus J Riemenschneider; Eliezer Masliah; Fred H Gage; Jürgen Winkler
Journal:  Acta Neuropathol       Date:  2016-04-08       Impact factor: 17.088

3.  Apolipoprotein E ε4 Mediates Myelin Breakdown by Targeting Oligodendrocytes in Sporadic Alzheimer Disease.

Authors:  Gerald Wai-Yeung Cheng; Kingston King-Shi Mok; Sunny Hoi-Sang Yeung; Julia Kofler; Karl Herrup; Kai-Hei Tse
Journal:  J Neuropathol Exp Neurol       Date:  2022-08-16       Impact factor: 3.148

Review 4.  Oligodendroglia and Myelin in Neurodegenerative Diseases: More Than Just Bystanders?

Authors:  Benjamin Ettle; Johannes C M Schlachetzki; Jürgen Winkler
Journal:  Mol Neurobiol       Date:  2015-05-13       Impact factor: 5.590

5.  Dendritic retraction, but not atrophy, is consistent in amyotrophic lateral sclerosis-comparison between Onuf's neurons and other sacral motor neurons.

Authors:  Takahiro Takeda; Toshiki Uchihara; Yuki Nakayama; Ayako Nakamura; Shoichi Sasaki; Shinji Kakei; Shinichiro Uchiyama; Charles Duyckaerts; Mari Yoshida
Journal:  Acta Neuropathol Commun       Date:  2014-01-27       Impact factor: 7.801

Review 6.  Basic mechanisms of neurodegeneration: a critical update.

Authors:  Kurt A Jellinger
Journal:  J Cell Mol Med       Date:  2010-01-11       Impact factor: 5.310

  6 in total

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