Immunohistochemical localization of spatacsin in α-synucleinopathies.

Abstract

Spatacsin (SPG11) is a major mutated gene in autosomal recessive spastic paraplegia with thin corpus callosum (ARHSP-TCC) and is responsible for juvenile Parkinsonism. To elucidate the role of spatacsin in the pathogenesis of α-synucleinopathies, an immunohistochemical investigation was performed on the brain of patients with Parkinson's disease (PD), dementia with Lewy bodies (DLB) and multiple system atrophy (MSA) using anti-spatacsin antibody. In PD, Lewy bodies (LBs) in the brain stem were positive for spatacsin. These LBs showed intense staining in their peripheral portions and occasionally in the central cores. Lewy neurites were also spatacsin-positive. In DLB, cortical LBs were immunolabeled by spatacsin. In MSA, glial cytoplasmic inclusions (GCI) and a small fraction of neuronal cytoplasmic inclusions (NCI) were positive for spatacsin. The widespread accumulation of spatacsin observed in pathologic α-synuclein-containing inclusions suggests that spatacsin may be involved in the pathogenesis of α-synucleinopathies.

• Authors: Satoshi Kuru, Mari Yoshida, Shinsui Tatsumi, Maya Mimuro
• Journal: Neuropathology : official journal of the Japanese Society of Neuropathology (Neuropathology) Vol. 34 Issue 2 Pg. 135-9 (Apr 2014) ISSN: 1440-1789 [Electronic] Australia
• PMID: 24112408 (Publication Type: Journal Article)
• Copyright: © 2013 Japanese Society of Neuropathology.

Chemical References

• Proteins
• SPG11 protein, human
• alpha-Synuclein

Topics

• Aged
• Aged, 80 and over
• Autopsy
• Brain (pathology)
• Female
• Humans
• Immunohistochemistry
• Inclusion Bodies (metabolism, pathology)
• Lewy Body Disease (pathology)
• Male
• Middle Aged
• Multiple System Atrophy (pathology)
• Parkinson Disease (pathology)
• Proteins (metabolism)
• Temporal Lobe (metabolism, pathology)
• alpha-Synuclein (metabolism)