4.6 Article

Immunocytochemical localization of synphilin-1, an alpha-synuclein-associated protein, in neurodegenerative disorders

期刊

ACTA NEUROPATHOLOGICA
卷 103, 期 3, 页码 209-214

出版社

SPRINGER-VERLAG
DOI: 10.1007/s004010100451

关键词

alpha-synuclein; glial cytoplasmic inclusion; Lewy body; multiple system atrophy; synphilin-1

资金

  1. NINDS NIH HHS [NS 38377, NS 16375] Funding Source: Medline
  2. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [P50NS038377, P01NS016375, P50NS016375] Funding Source: NIH RePORTER

向作者/读者索取更多资源

alpha-Synuclein is a major component of Lewy bodies (LB) in Parkinson's disease (PD) and dementia with LB (DLB). as well as of glial cytoplasmic inclusions (GCI) in multiple system atrophy (MSA). Recently, a novel protein called synphilin-1 has been identified that associates with alpha-synuclein, and it has been reported that cotransfection of both a-synuclein and synphilin-1 in mammalian cells yielded eosinophilic cytoplasmic inclusions resembling LB. Immunocytochemical and ultrastructural investigations have now been performed on the brain of patients with various neurodegenerative disorders using anti-synphilin-1 antibodies. These antibodies immunostained the neuropil in a punctate pattern throughout the brain of control subjects. In PD. most LB observed in the brain stem were positive for synphilin-1. These LB showed intense staining in their central cores, but their peripheral portions were only weakly stained or unstained. Pale bodies and Lewy neurites, which were positive for alpha-synuclein, were synphilin-1 negative. In DLB, a small fraction of cortical LB were immunolabeled by anti-synphilin-1.

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