Emerging evidence for cell-autonomous axon guidance.
Hidekiyo HaradaJason CharishPhilippe P MonnierPublished in: Development, growth & differentiation (2020)
Current models of axon guidance within the central nervous system (CNS) involve the presentation of environmental cues to navigating growth cones. The surrounding and target tissues present a variety of ligands that either restrict or promote growth, thus providing pathfinding instructions to developing axons. Recent findings show that RGMb, a GPI anchored extracellular protein present on retinal ganglion cells, down-regulates Wnt3a signaling by lowering LRP5 levels at the membrane surface. When RGMb is phosphorylated by the extracellular tyrosine kinase VLK, phosphorylated RGMb (p-RGMb) is internalized and carries LRP5 towards intracellular compartments. In the eye, a dorsal-high ventral-low gradient of VLK generates a dorsal-low ventral-high gradient of LRP5 that modulates Wnt3a signaling. These molecules, which are all expressed by individual RGCs, generate Wnt-signal gradients along the dorso-ventral axis of the retina, resulting in differential axon growth which in turn regulates proper retino-tectal/collicular map formation. This pathway represents a regulatory mechanism whereby extracellular phosphorylation generates what may be the first example of a unique self-guiding mechanism that affects neuronal-target connections independent of paracrine signals from the surrounding target tissue.
Keyphrases
- spinal cord
- tyrosine kinase
- cell proliferation
- stem cells
- neuropathic pain
- deep brain stimulation
- optic nerve
- epidermal growth factor receptor
- induced apoptosis
- spinal cord injury
- gene expression
- prefrontal cortex
- single cell
- transcription factor
- diabetic retinopathy
- cell therapy
- fluorescent probe
- blood brain barrier
- mesenchymal stem cells
- oxidative stress
- binding protein
- amino acid
- cell cycle arrest
- low density lipoprotein
- small molecule
- living cells
- endoplasmic reticulum stress