Article

Immunohistochemical localization of X-linked inhibitor of apoptosis protein in brainstem-type and cortical Lewy bodies.

Department of Neurology, Faculty of Medicine, Kyoto University, Sakyoku, Kyoto, Japan.
Neuroreport (impact factor: 1.66). 02/2012; 23(3):162-7. DOI:10.1097/WNR.0b013e32834f4066 pp.162-7
Source: PubMed

ABSTRACT X-linked inhibitor of apoptosis protein (XIAP) blocks the apoptosis by binding to and inhibiting caspases-3, 7, and 9. XIAP is negatively regulated by the mitochondrial serine protease, HtrA2/Omi. The aim of this study was to investigate the role of XIAP and the relationship between XIAP and HtrA2/Omi in patients with Parkinson's disease or dementia with Lewy bodies. We conducted immunohistochemical studies on XIAP in formalin-fixed, paraffin-embedded sections from eight normal participants, 10 patients with Parkinson's disease, five patients with dementia with Lewy bodies, and seven patients with Alzheimer's disease, and then double-labeling immunohistochemistry for XIAP and HtrA2/Omi in sections from the Parkinson's disease and dementia with Lewy bodies cases. Brainstem-type and cortical Lewy bodies were intensely immunostained for XIAP, and XIAP immunoreactivity was localized to the halos of brainstem-type Lewy bodies and to the entire bodies of cortical Lewy bodies. Double immunofluorescence analyses showed that XIAP and HtrA2/Omi immunoreactivities were colocalized to both types of Lewy bodies. Our results suggest that XIAP may be partially associated with the pathogenesis of Parkinson's disease and dementia with Lewy bodies.

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Keywords

10 patients
 
Alzheimer's disease
 
apoptosis protein
 
brainstem-type Lewy bodies
 
cortical Lewy bodies
 
double-labeling immunohistochemistry
 
entire bodies
 
HtrA2/Omi immunoreactivities
 
immunofluorescence analyses
 
immunohistochemical studies
 
inhibiting caspases-3
 
Lewy bodies
 
Lewy bodies cases
 
mitochondrial serine protease
 
normal participants
 
paraffin-embedded sections
 
Parkinson's disease
 
X-linked inhibitor
 
XIAP
 
XIAP immunoreactivity