The role of the diencephalon in the guidance of thalamocortical axons in mice

Development. 2020 Jun 26;147(12):dev184523. doi: 10.1242/dev.184523.

Abstract

Thalamocortical axons (TCAs) cross several tissues on their journey to the cortex. Mechanisms must be in place along the route to ensure they connect with their targets in an orderly fashion. The ventral telencephalon acts as an instructive tissue, but the importance of the diencephalon in TCA mapping is unknown. We report that disruption of diencephalic development by Pax6 deletion results in a thalamocortical projection containing mapping errors. We used conditional mutagenesis to test whether these errors are due to the disruption of pioneer projections from prethalamus to thalamus and found that, although this correlates with abnormal TCA fasciculation, it does not induce topographical errors. To test whether the thalamus contains navigational cues for TCAs, we used slice culture transplants and gene expression studies. We found the thalamic environment is instructive for TCA navigation and that the molecular cues netrin 1 and semaphorin 3a are likely to be involved. Our findings indicate that the correct topographic mapping of TCAs onto the cortex requires the order to be established from the earliest stages of their growth by molecular cues in the thalamus itself.

Keywords: Axon guidance; Diencephalon; Pax6; Prethalamic pioneer axons; Thalamocortical tract; Thalamus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axons / physiology*
  • Diencephalon / metabolism*
  • Diencephalon / pathology
  • Embryo, Mammalian / metabolism
  • Embryo, Mammalian / pathology
  • Gene Expression Regulation, Developmental
  • Homeodomain Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Mice, Knockout
  • Mutagenesis
  • Netrin-1 / metabolism
  • Organ Culture Techniques
  • PAX6 Transcription Factor / deficiency
  • PAX6 Transcription Factor / genetics
  • PAX6 Transcription Factor / metabolism
  • Semaphorin-3A / metabolism
  • Thalamus / metabolism*
  • Thalamus / pathology

Substances

  • Gsh2 protein, mouse
  • Homeodomain Proteins
  • Ntn1 protein, mouse
  • PAX6 Transcription Factor
  • Pax6 protein, mouse
  • Semaphorin-3A
  • Netrin-1