Correlating STED and synchrotron XRF nano-imaging unveils cosegregation of metals and cytoskeleton proteins in dendrites.
Florelle DomartPeter CloetensStéphane RoudeauAsuncion CarmonaEmeline VerdierDaniel ChoquetRichard OrtegaPublished in: eLife (2020)
Zinc and copper are involved in neuronal differentiation and synaptic plasticity but the molecular mechanisms behind these processes are still elusive due in part to the difficulty of imaging trace metals together with proteins at the synaptic level. We correlate stimulated-emission-depletion microscopy of proteins and synchrotron X-ray fluorescence imaging of trace metals, both performed with 40 nm spatial resolution, on primary rat hippocampal neurons. We reveal the co-localization at the nanoscale of zinc and tubulin in dendrites with a molecular ratio of about one zinc atom per tubulin-αβ dimer. We observe the co-segregation of copper and F-actin within the nano-architecture of dendritic protrusions. In addition, zinc chelation causes a decrease in the expression of cytoskeleton proteins in dendrites and spines. Overall, these results indicate new functions for zinc and copper in the modulation of the cytoskeleton morphology in dendrites, a mechanism associated to neuronal plasticity and memory formation.
Keyphrases
- oxide nanoparticles
- fluorescence imaging
- high resolution
- photodynamic therapy
- single molecule
- human health
- health risk
- poor prognosis
- cerebral ischemia
- health risk assessment
- high throughput
- spinal cord
- dna methylation
- working memory
- brain injury
- genome wide
- mass spectrometry
- blood brain barrier
- subarachnoid hemorrhage
- spinal cord injury
- climate change
- binding protein
- high speed
- drinking water
- dual energy