TY - JOUR
T1 - Vesicular glutamate transporter 1 (VGLUT1)-and VGLUT2-containing terminals on the rat jaw-closing γ-Motoneurons
AU - Park, Sook Kyung
AU - Hong, Jae Hyun
AU - Jung, Jae Kwang
AU - Ko, Hyoung Gon
AU - Bae, Yong Chul
N1 - Publisher Copyright:
© 2019 Korean Society for Neurodegenerative Disease. All rights reserved.
PY - 2019
Y1 - 2019
N2 - Currently, compared to jaw-closing (JC) γ-motoneurons, the information on the distribution and morphology of glutamatergic synapses on the jaw-closing (JC) γ-motoneurons, which may help elucidate the mechanism of isometric contraction of the JC muscle, is very limited. This study investigated the distribution and ultrastructural features of vesicular glutamate transporter 1 (VGLUT1)- and VGLUT2-immunopositive (+) axon terminals (boutons) on JC γ-motoneurons by retrograde tracing with horseradish peroxidase, electron microscopic immunocytochemistry, and quantitative analysis. About 35% of the boutons on identified JC γ-motoneurons were VGLUT+, and of those, 99% were VGLUT2+. The fraction of VGLUT1+ boutons of all boutons and the percentage of membrane of JC γ-motoneurons covered by these boutons were significantly lower than those for the JC α-motoneurons, revealed in our previous work. The bouton volume, mitochondrial volume, and active zone area of the VGLUT2+ boutons on the JC γ-motoneurons were uniformly small. These findings suggest that the JC γ-motoneurons, in contrast to the JC α-motoneurons, receive generally weak glutamatergic synaptic input almost exclusively from VGLUT2+ premotoneurons that form direct synapse with motoneurons.
AB - Currently, compared to jaw-closing (JC) γ-motoneurons, the information on the distribution and morphology of glutamatergic synapses on the jaw-closing (JC) γ-motoneurons, which may help elucidate the mechanism of isometric contraction of the JC muscle, is very limited. This study investigated the distribution and ultrastructural features of vesicular glutamate transporter 1 (VGLUT1)- and VGLUT2-immunopositive (+) axon terminals (boutons) on JC γ-motoneurons by retrograde tracing with horseradish peroxidase, electron microscopic immunocytochemistry, and quantitative analysis. About 35% of the boutons on identified JC γ-motoneurons were VGLUT+, and of those, 99% were VGLUT2+. The fraction of VGLUT1+ boutons of all boutons and the percentage of membrane of JC γ-motoneurons covered by these boutons were significantly lower than those for the JC α-motoneurons, revealed in our previous work. The bouton volume, mitochondrial volume, and active zone area of the VGLUT2+ boutons on the JC γ-motoneurons were uniformly small. These findings suggest that the JC γ-motoneurons, in contrast to the JC α-motoneurons, receive generally weak glutamatergic synaptic input almost exclusively from VGLUT2+ premotoneurons that form direct synapse with motoneurons.
KW - Electron microscopy
KW - Glutamatergic synapse
KW - Immunohistochemistry
KW - Jaw closing γ-motoneuron
KW - Vesicular glutamate transporter
UR - http://www.scopus.com/inward/record.url?scp=85073371472&partnerID=8YFLogxK
U2 - 10.5607/en.2019.28.4.451
DO - 10.5607/en.2019.28.4.451
M3 - Article
AN - SCOPUS:85073371472
SN - 1226-2560
VL - 28
SP - 451
EP - 457
JO - Experimental Neurobiology
JF - Experimental Neurobiology
IS - 4
ER -