Feedback Synthesizes Neural Codes for Motion

Curr Biol. 2017 May 8;27(9):1356-1361. doi: 10.1016/j.cub.2017.03.068. Epub 2017 Apr 27.

Abstract

In senses as diverse as vision, hearing, touch, and the electrosense, sensory neurons receive bottom-up input from the environment, as well as top-down input from feedback loops involving higher brain regions [1-4]. Through connectivity with local inhibitory interneurons, these feedback loops can exert both positive and negative control over fundamental aspects of neural coding, including bursting [5, 6] and synchronous population activity [7, 8]. Here we show that a prominent midbrain feedback loop synthesizes a neural code for motion reversal in the hindbrain electrosensory ON- and OFF-type pyramidal cells. This top-down mechanism generates an accurate bidirectional encoding of object position, despite the inability of the electrosensory afferents to generate a consistent bottom-up representation [9, 10]. The net positive activity of this midbrain feedback is additionally regulated through a hindbrain feedback loop, which reduces stimulus-induced bursting and also dampens the ON and OFF cell responses to interfering sensory input [11]. We demonstrate that synthesis of motion representations and cancellation of distracting signals are mediated simultaneously by feedback, satisfying an accepted definition of spatial attention [12]. The balance of excitatory and inhibitory feedback establishes a "focal" distance for optimized neural coding, whose connection to a classic motion-tracking behavior provides new insight into the computational roles of feedback and active dendrites in spatial localization [13, 14].

Keywords: ON and OFF cells; burst spiking; cerebellum; electric fish; gain control; motion tracking; neural coding; spatial attention; top-down processing; topographic feedback.

MeSH terms

  • Action Potentials
  • Animals
  • Electric Fish / physiology*
  • Electric Organ
  • Electric Stimulation
  • Feedback, Physiological*
  • Motion
  • Neural Pathways / metabolism*
  • Pyramidal Cells / metabolism
  • Rhombencephalon / cytology
  • Rhombencephalon / metabolism
  • Sensory Receptor Cells / cytology
  • Sensory Receptor Cells / physiology*