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Nano-Infrared Imaging of Primary Neurons.

Raul de Oliveira FreitasAdrian CernescuAnders EngdahlAgnes PaulusJoão E LevandoskiIsak MartinssonElke HebischChristophe SandtGunnar Keppler GourasChristelle N PrinzTomas DeierborgFerenc BorondicsOxana Klementieva
Published in: Cells (2021)
Alzheimer's disease (AD) accounts for about 70% of neurodegenerative diseases and is a cause of cognitive decline and death for one-third of seniors. AD is currently underdiagnosed, and it cannot be effectively prevented. Aggregation of amyloid-β (Aβ) proteins has been linked to the development of AD, and it has been established that, under pathological conditions, Aβ proteins undergo structural changes to form β-sheet structures that are considered neurotoxic. Numerous intensive in vitro studies have provided detailed information about amyloid polymorphs; however, little is known on how amyloid β-sheet-enriched aggregates can cause neurotoxicity in relevant settings. We used scattering-type scanning near-field optical microscopy (s-SNOM) to study amyloid structures at the nanoscale, in individual neurons. Specifically, we show that in well-validated systems, s-SNOM can detect amyloid β-sheet structures with nanometer spatial resolution in individual neurons. This is a proof-of-concept study to demonstrate that s-SNOM can be used to detect Aβ-sheet structures on cell surfaces at the nanoscale. Furthermore, this study is intended to raise neurobiologists' awareness of the potential of s-SNOM as a tool for analyzing amyloid β-sheet structures at the nanoscale in neurons without the need for immunolabeling.
Keyphrases
  • high resolution
  • cognitive decline
  • spinal cord
  • mild cognitive impairment
  • mass spectrometry
  • stem cells
  • healthcare
  • staphylococcus aureus
  • cystic fibrosis
  • optical coherence tomography
  • high throughput