期刊
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
卷 43, 期 7, 页码 604-620出版社
WILEY
DOI: 10.1111/nan.12402
关键词
amyloid; conformation-selective antibodies; Lewy pathology maturation; Parkinson's disease
资金
- NIH/NIA training grant [T32-AG000255]
- NIH/NINDS Morris K. Udall Parkinson's Disease Center of Excellence [P50 NS053488]
- Michael J. Fox Foundation
- Keefer family
- Parkinson Council
- Parkinson's Disease Foundation Summer Student Fellowship [PDF-SFW-1562]
- NIH [K08-NS093127]
Aims: The aim of this study was to test the hypothesis that different conformations of misfolded alpha-synuclein (alpha-syn) are present in Parkinson's disease (PD) brain. Methods: Using two previously characterized conformations of a-syn fibrils, we generated new conformationselective a-syn monoclonal antibodies (mAbs). We then interrogated multiple brain regions in a well-characterized autopsy cohort of PD patients (n = 49) with these mAbs, Syn7015 and Syn9029. Results: Syn7015 detects Lewy bodies (LBs) and Lewy neurites (LNs) formed by pathological alpha-syn in all brain regions tested, and is particularly sensitive to LNs and small Lewy dots, inclusions believed to form early in the disease. Further, we observed colocalization between Syn7015 and an early marker of alpha-syn pathology formation, phosphoSer129-alpha-syn, and a lack of extensive colocalization with markers of more mature pathology. In comparison, Syn9029 detects Lewy pathology in all regions examined, but indicates significantly fewer LNs than Syn7015. In addition, colocalization of Syn9029 with later markers of alpha-syn pathology maturation (ubiquitin and P62) suggests that the pathology detected by Syn9029 is older. Semiquantitative scoring of both LN and LB pathology in nine brain regions further established this trend, with Syn7015 LN scores consistently higher than Syn9029 LN scores. Conclusions: Our data indicate that different conformations of alpha-syn pathology are present in PD brain and correspond to different stages of maturity for Lewy pathology. Regional analysis of Syn7015 and Syn9029 immunostaining also provides support for the Braak hypothesis that alpha-syn pathology advances through the brain.
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