Remote control of neural function by X-ray-induced scintillation

Nat Commun. 2021 Jul 22;12(1):4478. doi: 10.1038/s41467-021-24717-1.

Abstract

Scintillators emit visible luminescence when irradiated with X-rays. Given the unlimited tissue penetration of X-rays, the employment of scintillators could enable remote optogenetic control of neural functions at any depth of the brain. Here we show that a yellow-emitting inorganic scintillator, Ce-doped Gd3(Al,Ga)5O12 (Ce:GAGG), can effectively activate red-shifted excitatory and inhibitory opsins, ChRmine and GtACR1, respectively. Using injectable Ce:GAGG microparticles, we successfully activated and inhibited midbrain dopamine neurons in freely moving mice by X-ray irradiation, producing bidirectional modulation of place preference behavior. Ce:GAGG microparticles are non-cytotoxic and biocompatible, allowing for chronic implantation. Pulsed X-ray irradiation at a clinical dose level is sufficient to elicit behavioral changes without reducing the number of radiosensitive cells in the brain and bone marrow. Thus, scintillator-mediated optogenetics enables minimally invasive, wireless control of cellular functions at any tissue depth in living animals, expanding X-ray applications to functional studies of biology and medicine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal / physiology
  • Behavior, Animal / radiation effects
  • Brain / physiology*
  • Brain / radiation effects
  • Cerium
  • Female
  • HEK293 Cells
  • Humans
  • Luminescence
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Opsins / metabolism
  • Opsins / radiation effects
  • Optogenetics / instrumentation
  • Scintillation Counting
  • Wireless Technology / instrumentation
  • X-Rays

Substances

  • Opsins
  • Cerium