TY - JOUR
T1 - Neuronal intranuclear inclusion disease in a horse
AU - Pumarola, M.
AU - Vidal, E.
AU - Trens, J. M.
AU - Serafín, A.
AU - Ferrer, I.
N1 - Funding Information:
Acknowledgements This work was supported in part by the CIEN project: FIS grant C003–006. Ultrastructural studies were carried our in the Electron Microscopy Service of the Universitat Autò-noma de Barcelona. We thank T. Yohannan for editorial assistance.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2005/8/1
Y1 - 2005/8/1
N2 - Neuronal intranuclear inclusion disease (NIID) is reported in a 16-year-old Pure Spanish breed female horse suffering from progressive ataxia and motor deficiencies. The neuropathological study revealed NIIs throughout the central nervous system, although mainly in the brain stem and spinal cord. This distribution did not correlate with neuron loss, which was marked in the hippocampus and moderate in the neocortex, particularly in the occipital cortex. As in humans, NIIs in the horse were hyaline autofluorescent inclusions composed of non-membrane-bound aggregates of filaments and fine granules. NIIs were stained with anti-ubiquitin and anti-clusterin antibodies. In addition, NIIs were stained with antibodies raised against subunits of the 19S and PA28, but not of the 20S, components of the proteasome. These observations indicate similarities between NIID in humans and horses, and suggest that clusterin and abnormal ubiquitin-proteasomal expression participate in NII formation. © Springer-Verlag 2005.
AB - Neuronal intranuclear inclusion disease (NIID) is reported in a 16-year-old Pure Spanish breed female horse suffering from progressive ataxia and motor deficiencies. The neuropathological study revealed NIIs throughout the central nervous system, although mainly in the brain stem and spinal cord. This distribution did not correlate with neuron loss, which was marked in the hippocampus and moderate in the neocortex, particularly in the occipital cortex. As in humans, NIIs in the horse were hyaline autofluorescent inclusions composed of non-membrane-bound aggregates of filaments and fine granules. NIIs were stained with anti-ubiquitin and anti-clusterin antibodies. In addition, NIIs were stained with antibodies raised against subunits of the 19S and PA28, but not of the 20S, components of the proteasome. These observations indicate similarities between NIID in humans and horses, and suggest that clusterin and abnormal ubiquitin-proteasomal expression participate in NII formation. © Springer-Verlag 2005.
KW - Clusterin
KW - Horse
KW - Neuronal intranuclear inclusion
KW - Proteasome
UR - http://www.scopus.com/inward/record.url?scp=24344482470&partnerID=8YFLogxK
U2 - 10.1007/s00401-005-1033-5
DO - 10.1007/s00401-005-1033-5
M3 - Article
C2 - 15971054
SN - 0001-6322
VL - 110
SP - 191
EP - 195
JO - Acta Neuropathologica
JF - Acta Neuropathologica
IS - 2
ER -