TY - JOUR
T1 - Optogenetic examination of prefrontal-amygdala synaptic development
AU - Arruda-Carvalho, Maithe
AU - Wu, Wan Chen
AU - Cummings, Kirstie A.
AU - Clem, Roger L.
N1 - Publisher Copyright:
© 2017 the authors.
PY - 2017/3/15
Y1 - 2017/3/15
N2 - A brain network comprising the medial prefrontal cortex (mPFC) and amygdala plays important roles in developmentally regulated cognitive and emotional processes. However, very little is known about the maturation of mPFC-amygdala circuitry. We conducted anatomical tracing of mPFC projections and optogenetic interrogation of their synaptic connections with neurons in the basolateral amygdala (BLA) at neonatal to adult developmental stages in mice. Results indicate that mPFC-BLA projections exhibit delayed emergence relative to other mPFC pathways and establish synaptic transmission with BLA excitatory and inhibitory neurons in late infancy, events that coincide with a massive increase in overall synaptic drive. During subsequent adolescence, mPFC-BLA circuits are further modified by excitatory synaptic strengthening as well as a transient surge in feedforward inhibition. The latter was correlated with increased spontaneous inhibitory currents in excitatory neurons, suggesting thatmPFC-BLAcircuit maturation culminates in a period of exuberant GABAergic transmission. These findings establish a time course for the onset and refinement of mPFC-BLA transmission and point to potential sensitive periods in the development of this critical network.
AB - A brain network comprising the medial prefrontal cortex (mPFC) and amygdala plays important roles in developmentally regulated cognitive and emotional processes. However, very little is known about the maturation of mPFC-amygdala circuitry. We conducted anatomical tracing of mPFC projections and optogenetic interrogation of their synaptic connections with neurons in the basolateral amygdala (BLA) at neonatal to adult developmental stages in mice. Results indicate that mPFC-BLA projections exhibit delayed emergence relative to other mPFC pathways and establish synaptic transmission with BLA excitatory and inhibitory neurons in late infancy, events that coincide with a massive increase in overall synaptic drive. During subsequent adolescence, mPFC-BLA circuits are further modified by excitatory synaptic strengthening as well as a transient surge in feedforward inhibition. The latter was correlated with increased spontaneous inhibitory currents in excitatory neurons, suggesting thatmPFC-BLAcircuit maturation culminates in a period of exuberant GABAergic transmission. These findings establish a time course for the onset and refinement of mPFC-BLA transmission and point to potential sensitive periods in the development of this critical network.
KW - Adolescence
KW - Amygdala
KW - Prefrontal development
UR - https://www.scopus.com/pages/publications/85015288235
U2 - 10.1523/JNEUROSCI.3097-16.2017
DO - 10.1523/JNEUROSCI.3097-16.2017
M3 - Article
C2 - 28193691
AN - SCOPUS:85015288235
SN - 0270-6474
VL - 37
SP - 2976
EP - 2985
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 11
ER -