Parallel enlargement of Marinesco bodies and nuclei and progressive deposition of p62 in pigmented neurons of the substantia nigra

2020 ◽  
Vol 40 (4) ◽  
pp. 328-335
Author(s):  
Ryota Amano ◽  
Shuta Toru ◽  
Michio Yamane ◽  
Masanobu Kitagawa ◽  
Katsuiku Hirokawa ◽  
...  
2002 ◽  
Vol 176 (1) ◽  
pp. 117-121 ◽  
Author(s):  
Mattias Kettner ◽  
Dirk Willwohl ◽  
Gene B. Hubbard ◽  
U. Rüb ◽  
Edward J. Dick ◽  
...  

2016 ◽  
Vol 46 (7) ◽  
pp. 839-842
Author(s):  
I. P. Grigor’ev ◽  
V. V. Gusel’nikova ◽  
E. G. Sukhorukova ◽  
D. E. Korzhevskii

Acta Naturae ◽  
2017 ◽  
Vol 9 (3) ◽  
pp. 81-88 ◽  
Author(s):  
D. E. Korzhevskii ◽  
V. V. Gusel’nikova ◽  
O. V. Kirik ◽  
E. G. Sukhorukova ◽  
I. P. Grigorev

We studied the intranuclear localization of protein nucleophosmin (B23) and ubiquitin in the dopaminergic neurons of human substantia nigra (n = 6, age of 25-87 years) using immunohistochemistry and confocal laser microscopy. Intranuclear ubiquitin-immunopositive bodies that morphologically correspond to Marinesco bodies were found to be present in substantia nigra dopaminergic (tyrosine hydroxylase-immunopositive) neurons but absent in non-dopaminergic neurons. The number of bodies varied from 0 to 6 per cell nucleus. Nucleophosmin (B23) was found in the neuronal nucleolus, with the nucleolus size being constant in the nigral neurons of each individual brain. All the observed neurons had only one large nucleolus with intense nucleophosmin immunoreactivity and a lightly stained region (1-2 m in diameter) that apparently represents the giant fibrillar center (GFC). An intensely immunostained nucleophosmin-containing granule was often observed at the GFC periphery. Double labeling demonstrated that nucleophosmin-immunoreactive nucleolus and ubiquitin-immunoreactive Marinesco bodies can occur both closely to and remotely from each other. Three-dimensional reconstruction indicates that rounded Marinesco bodies are polymorphic and often have a complex shape, with some flattening and concavities, which may be associated with contact not only with the nucleolus, but also, presumably, with other intranuclear structures free of ubiquitin or nucleophosmin. Ubiquitin-immunoreactive structures with a relatively small size (up to 1 m in length) and various clastosome-like shapes (Lafarga et al., 2002) often occur near Marinesco bodies. There were no cases of detection of ubiquitin in the nucleoli of dopaminergic neurons and nucleophosmin/B23 in typical Marinesco bodies. The obtained information may be helpful in unraveling the molecular mechanisms of the selective vulnerability of substantia nigra dopaminergic neurons to damaging factors.


2004 ◽  
Vol 63 (4) ◽  
pp. 329-337 ◽  
Author(s):  
Thomas G. Beach ◽  
Douglas G. Walker ◽  
Lucia I. Sue ◽  
Amanda Newell ◽  
Charles C. Adler ◽  
...  

2017 ◽  
Vol 43 (7) ◽  
pp. 621-630 ◽  
Author(s):  
R. D. Abbott ◽  
J. S. Nelson ◽  
G.W. Ross ◽  
J. H. Uyehara-Lock ◽  
C. M. Tanner ◽  
...  

Author(s):  
Jorge Pecci Saavedra ◽  
Mark Connaughton ◽  
Juan José López ◽  
Alicia Brusco

The use of antibodies as labels for the localization of specific molecules in the nervous systan has been extensively applied in recent years. Both monoand polyclonal antibodies or antisera have been employed. The knowledge of the organization of neuronal connectivities, gliovascular relationships, glioneuronal relationships and other features of nerve tissue has greatly increased.A number of areas of the nervous systan have been analyzed in our laboratory, including the nuclei of the raphe system, the reticular formation, interpeduncular nucleus, substantia nigra, caudate nucleus, putamen, pallidum, spinal cord, pineal gland and others.From a technical point of view, a number of variables needed to be taken into account in order to obtain reliable and reproducible results. The design of the optimal conditions of tissue fixation, embedding, sectioning, dilution of antibodies, and adaptation of Sternberger PAP technique were sane of the parameters taken into account to optimize the results. It is critical that each step of the technique be defined for each particular case.


1996 ◽  
Vol 22 (3) ◽  
pp. 228-232 ◽  
Author(s):  
D. A. McRitchie ◽  
G. M. Halliday ◽  
R. Pamphlett

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