Distinct developmental origins manifest in the specialized encoding of movement by adult neurons of the external globus pallidus

Neuron. 2015 Apr 22;86(2):501-13. doi: 10.1016/j.neuron.2015.03.007. Epub 2015 Apr 2.

Abstract

Transcriptional codes initiated during brain development are ultimately realized in adulthood as distinct cell types performing specialized roles in behavior. Focusing on the mouse external globus pallidus (GPe), we demonstrate that the potential contributions of two GABAergic GPe cell types to voluntary action are fated from early life to be distinct. Prototypic GPe neurons derive from the medial ganglionic eminence of the embryonic subpallium and express the transcription factor Nkx2-1. These neurons fire at high rates during alert rest, and encode movements through heterogeneous firing rate changes, with many neurons decreasing their activity. In contrast, arkypallidal GPe neurons originate from lateral/caudal ganglionic eminences, express the transcription factor FoxP2, fire at low rates during rest, and encode movements with robust increases in firing. We conclude that developmental diversity positions prototypic and arkypallidal neurons to fulfil distinct roles in behavior via their disparate regulation of GABA release onto different basal ganglia targets.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology
  • Animals
  • Cell Lineage / physiology
  • Enkephalins / metabolism
  • Forkhead Transcription Factors / metabolism*
  • Globus Pallidus / cytology*
  • Globus Pallidus / embryology
  • Globus Pallidus / growth & development*
  • Mice
  • Movement / physiology*
  • Neurons / classification*
  • Neurons / metabolism*
  • Nuclear Proteins / metabolism*
  • Protein Precursors / metabolism
  • ROC Curve
  • Repressor Proteins / metabolism*
  • Thyroid Nuclear Factor 1
  • Transcription Factors / metabolism*
  • gamma-Aminobutyric Acid / metabolism

Substances

  • Enkephalins
  • Forkhead Transcription Factors
  • Foxp2 protein, mouse
  • Nkx2-1 protein, mouse
  • Nuclear Proteins
  • Protein Precursors
  • Repressor Proteins
  • Thyroid Nuclear Factor 1
  • Transcription Factors
  • gamma-Aminobutyric Acid
  • preproenkephalin