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◆ bioRxiv : the preprint server for biology2026-09-16· neuroscience

Semaphorin 3G (SEMA3G) is a highly selective marker of cerebral amyloid angiopathy.

Kaleah Balcomb, Jessica Buchanan, Aysha Strobbe, Daphne Claus, Arline Faustin, Julie Schneider, Thomas Wisniewski, Margaret Sunde, Eleanor Drummond

原始摘要(英文原文)· Original abstract
Biomarkers of cerebral amyloid angiopathy (CAA) are critically needed. We recently identified semaphorin 3G (SEMA3G) as a novel protein selectively enriched in CAA. Here, we aimed to determine if SEMA3G was a selective marker of CAA in a large cohort of human brain tissue spanning multiple neurodegenerative diseases and three brain regions, and to determine if SEMA3G directly interacts with amyloid beta (Aβ). Multiplexed immunofluorescence showed that SEMA3G significantly accumulated only in CAA + blood vessels in the brain in all cases. We also showed that SEMA3G preferentially associated with Aβ 40 , Aβ pS8 and Aβ pE3, but not Aβ 42 . Thioflavin T assays and transmission electron microscopy showed that SEMA3G directly interacted with Aβ and slowed Aβ aggregation in vitro , and that this effect was more pronounced for Aβ 40 than Aβ 42 . Together our results demonstrate that SEMA3G is a highly specific marker of CAA in the brain.
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Semaphorin 3G (SEMA3G) is a highly selective marker of cerebral amyloid angiopathy. — 科研速览 Science Skim