2024-03-28T21:14:02Zhttp://digital.csic.es/dspace-oai/requestoai:digital.csic.es:10261/628632016-02-17T11:07:14Zcom_10261_133com_10261_1col_10261_386
Development of "pinceaux" formations and dendritic translocation of climbing fibers during the acquisition of the balance between glutamatergic and γ-aminobutyric acidergic inputs in developing purkinje cells
Sotelo, Constantino
The acquisition of the dynamic balance between excitation and inhibition in developing Purkinje cells, necessary for their proper function, is analyzed. Newborn (PO) mouse cerebellum contains glutamatergic (VGLUT2-IR) and γ-aminobutyric acid (GABA)-ergic (VIAAT-IR) axons. The former prevail and belong to climbing fibers, whereas the latter neither colabel with calbindin-expressing fibers nor belong to axons of the cortical GABAergic interneurons. During the first postnatal week, VIAAT-IR axons in the Purkinje cell neighborhood remains very low, and the first synapses with basket fibers are formed at P7, when climbing fibers have already established dense pericellular nets. The descending basket fibers reach the Purkinje cell axon initial segment by P9, immediately establishing axoaxonic synapses. The pinceaux appear as primitive vortex-like arrangements by P12, and by P20 interbasket fiber septate-like junctions, typical of fully mature pinceaux, are still missing. The climbing fiber's somatodendritic translocation occurs later than expected, after the regression of the multiple innervation, and follows the ascending collaterals of the basket axons, which are apparently the optimal substrate for the proper subcellular targeting of the climbing fibers. These results emphasize that chemical transmission in the axon initial segment precedes the electrical inhibition generated by field effects. In addition, GABAergic Purkinje cells, as opposed to glutamatergic projection neurons in other cortical structures, do not begin to receive their excitation to inhibition balance until the end of the first postnatal week, despite the early presence of potentially functional GABAergic axons that possess the required vesicular transport system. © 2007 Wiley-lies, Inc.
2012-12-13T13:29:26Z
2012-12-13T13:29:26Z
2008
2012-12-13T13:29:26Z
artículo
Journal of Comparative Neurology 506(2): 240- 262 (2008)
http://hdl.handle.net/10261/62863
10.1002/cne.21501
eng
openAccess
Wiley-Liss