| First Author | Itoh Y | Year | 2023 |
| Journal | Cell Rep | Volume | 42 |
| Issue | 3 | Pages | 112182 |
| PubMed ID | 36934325 | Mgi Jnum | J:340983 |
| Mgi Id | MGI:7460974 | Doi | 10.1016/j.celrep.2023.112182 |
| Citation | Itoh Y, et al. (2023) Inter-axonal molecular crosstalk via Lumican proteoglycan sculpts murine cervical corticospinal innervation by distinct subpopulations. Cell Rep 42(3):112182 |
| abstractText | How CNS circuits sculpt their axonal arbors into spatially and functionally organized domains is not well understood. Segmental specificity of corticospinal connectivity is an exemplar for such regional specificity of many axon projections. Corticospinal neurons (CSN) innervate spinal and brainstem targets with segmental precision, controlling voluntary movement. Multiple molecularly distinct CSN subpopulations innervate the cervical cord for evolutionarily enhanced precision of forelimb movement. Evolutionarily newer CSN(BC-lat) exclusively innervate bulbar-cervical targets, while CSN(medial) are heterogeneous; distinct subpopulations extend axons to either bulbar-cervical or thoraco-lumbar segments. We identify that Lumican controls balance of cervical innervation between CSN(BC-lat) and CSN(medial) axons during development, which is maintained into maturity. Lumican, an extracellular proteoglycan expressed by CSN(BC-lat), non-cell-autonomously suppresses cervical collateralization by multiple CSN(medial) subpopulations. This inter-axonal molecular crosstalk between CSN subpopulations controls murine corticospinal circuitry refinement and forelimb dexterity. Such crosstalk is generalizable beyond the corticospinal system for evolutionary incorporation of new neuron populations into preexisting circuitry. |
