Role of Primary Afferents in the Developmental Regulation of Motor Axon Synapse Numbers on Renshaw Cells
Document Type
Article
Publication Date
6-15-2016
Abstract
Motor function in mammalian species depends on the maturation of spinal circuits formed by a large variety of interneurons that regulate motoneuron firing and motor output. Interneuron activity is in turn modulated by the organization of their synaptic inputs, but the principles governing the development of specific synaptic architectures unique to each premotor interneuron are unknown. For example, Renshaw cells receive, at least in the neonate, convergent inputs from sensory afferents (likely Ia) and motor axons, raising the question of whether they interact during Renshaw cell development. In other well-studied neurons, such as Purkinje cells, heterosynaptic competition between inputs from different sources shapes synaptic organization. To examine the possibility that sensory afferents modulate synaptic maturation on developing Renshaw cells, we used three animal models in which afferent inputs in the ventral horn are dramatically reduced (ER81−/−knockout), weakened (Egr3−/− knockout), or strengthened (mlcNT3+/− transgenic). We demonstrate that increasing the strength of sensory inputs on Renshaw cells prevents their deselection and reduces motor axon synaptic density, and, in contrast, absent or diminished sensory afferent inputs correlate with increased densities of motor axons synapses. No effects were observed on other glutamatergic inputs. We conclude that the early strength of Ia synapses influences their maintenance or weakening during later development and that heterosynaptic influences from sensory synapses during early development regulates the density and organization of motor inputs on mature Renshaw cells.
Repository Citation
Siembab, V. C.,
Gomez-Perez, L.,
Rotterman, T. M.,
Shneider, N. A.,
& Alvarez, F. J.
(2016). Role of Primary Afferents in the Developmental Regulation of Motor Axon Synapse Numbers on Renshaw Cells. Journal of Comparative Neurology, 524 (9), 1892-1919.
https://corescholar.libraries.wright.edu/ncbp/1093
DOI
10.1002/cne.23946