Abstract
The process of generating functionally distinct neocortical areas requires the formation of an intra-neocortical connectivity map. Here, we explore the early development of murine intra-neocortical projections and find that axons from rostral and caudal neurons remain, respectively, within large rostral and caudal domains of the neonatal neocortex. Despite evidence that thalamic input can regulate neocortical areal properties, we found that the neonatal intra-neocortical projection pattern was not perturbed when thalamic input was absent in Gbx2 mutants. On the contrary, in Fgf8 hypomorphic mutants, the rostral neocortex of which acquires more caudal molecular properties, caudally located neurons ectopically project axons into the rostral cortex. Therefore, neocortical patterning by Fgf8 also contributes to arealization through mediating early development of intra-neocortical connectivity.
MeSH Terms
Animals
Axons/physiology
Female
Fibroblast Growth Factor 8
Fibroblast Growth Factors/metabolism,physiology
Histocytochemistry
Homeodomain Proteins/genetics
In Situ Hybridization
Male
Mice
Mice, Inbred C57BL
Mice, Transgenic
Naphthalenes
Neocortex/cytology,embryology,metabolism
Neural Pathways/cytology,embryology,metabolism
Neurons/cytology,metabolism
Organophosphonates
Thalamus/physiology
Chemicals
Fgf8 protein, mouse
Gbx2 protein, mouse
Homeodomain Proteins
Naphthalenes
Organophosphonates
fluorescent phosphonate IVa
Fibroblast Growth Factor 8
Fibroblast Growth Factors
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Huffman Kelly J
Nina Ireland Laboratory of Developmental Neurobiology, Center for Neurobiology and Psychiatry, University of California, San Francisco, San Francisco, California 94143-0984, USA.
Garel Sonia
Rubenstein John L R
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