Topographical and cell type-specific connectivity of rostral and caudal forelimb corticospinal neuron populations
Cell Reports, ISSN: 2211-1247, Vol: 43, Issue: 4, Page: 113993
2024
- 7Citations
- 15Usage
- 12Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations7
- Citation Indexes7
- CrossRef7
- Usage15
- Downloads14
- Abstract Views1
- Captures12
- Readers12
- 12
Article Description
Corticospinal neurons (CSNs) synapse directly on spinal neurons, a diverse assortment of cells with unique structural and functional properties necessary for body movements. CSNs modulating forelimb behavior fractionate into caudal forelimb area (CFA) and rostral forelimb area (RFA) motor cortical populations. Despite their prominence, the full diversity of spinal neurons targeted by CFA and RFA CSNs is uncharted. Here, we use anatomical and RNA sequencing methods to show that CSNs synapse onto a remarkably selective group of spinal cell types, favoring inhibitory populations that regulate motoneuron activity and gate sensory feedback. CFA and RFA CSNs target similar spinal neuron types, with notable exceptions that suggest that these populations differ in how they influence behavior. Finally, axon collaterals of CFA and RFA CSNs target similar brain regions yet receive highly divergent inputs. These results detail the rules of CSN connectivity throughout the brain and spinal cord for two regions critical for forelimb behavior.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2211124724003218; http://dx.doi.org/10.1016/j.celrep.2024.113993; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85188959235&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/38551963; https://linkinghub.elsevier.com/retrieve/pii/S2211124724003218; https://digitalcommons.library.tmc.edu/uthmed_docs/777; https://digitalcommons.library.tmc.edu/cgi/viewcontent.cgi?article=1764&context=uthmed_docs; https://dx.doi.org/10.1016/j.celrep.2024.113993
Elsevier BV
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