Abstract

During development, two coordinated events shape the morphology of the mammalian cerebral cortex, leading to the cortex’s columnar and layered structure: the proliferation of neuronal progenitors and cortical migration. Pyramidal neurons originating from germinal zones migrate along radial glial fibers to their final position in the cortical plate by both radial migration and tangential dispersion. These processes rely on the delicate balance of intercellular adhesive and repulsive signaling that takes place between neurons interacting with different substrates and guidance cues. Here, we focus on the function of the cell adhesion molecules fibronectin leucine-rich repeat transmembrane proteins (FLRTs) in regulating both the radial migration of neurons, as well as their tangential spread, and the impact these processes have on cortex morphogenesis. In combining structural and functional analysis, recent studies have begun to reveal how FLRT-mediated responses are precisely tuned – from forming different protein complexes to modulate either cell adhesion or repulsion in neurons. These approaches provide a deeper understanding of the context-dependent interactions of FLRTs with multiple receptors involved in axon guidance and synapse formation that contribute to finely regulated neuronal migration.

Highlights

  • The cerebral cortex is an evolutionary advanced structure with complex functionality that is organized in two main axes: radial and tangential (Geschwind and Rakic, 2013)

  • Stripe assays showed that Lphn3 does not induce adhesion in HeLa cells expressing Unc5D and FLRT2, which contrasts to the strong adhesive response found in cells expressing FLRT2 alone or Unc5D with FLRT2UF mutant that binds Lphn3 but not Unc5 (Jackson et al, 2016). These results suggest that Unc5D acts as a switch modulating the adhesive properties of FLRT2-Lphn3 interaction, resembling the finding that Unc5B regulates FLRT3 adhesive properties (Karaulanov et al, 2009)

  • We recently showed that Latrophilins and Teneurins, known to promote synapse formation, are expressed in the cortex earlier in development, where they function in a complex with fibronectin leucine-rich repeat transmembrane proteins (FLRTs) to regulate radial migration by a contact-repulsion model

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Summary

Introduction

The cerebral cortex is an evolutionary advanced structure with complex functionality that is organized in two main axes: radial (vertical) and tangential (horizontal) (Geschwind and Rakic, 2013). Supporting this notion is the finding that some Unc5 receptors bind to Xenopus FLRT3 promoting cellular de-adhesion (Karaulanov et al, 2009), raising the possibility that similar interactions could provide guidance to migrating cells and/or pathfinding axons in other organisms.

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