| dc.description.abstract | The bed nucleus of the stria terminalis (BNST) is a critical mediator of stress responses and anxiety-like behaviors. Neurons expressing protein kinase C delta (BNST(PKCδ)) are an abundant but understudied subpopulation implicated in inhibiting feeding, but which have conflicting reports about their role in anxiety-like behaviors. We have previously shown that expression of PKCδ is dynamically regulated by stress. Here we first show that BNST(PKCδ) cells are recruited during bouts of active stress coping and receive input from the parabrachial nucleus. We then show that in vivo activation of this population is mildly aversive. This aversion was insensitive to prior restraint stress exposure. Further investigation revealed that unlike other BNST subpopulations, BNST(PKCδ) cells do not exhibit increased cfos expression following restraint stress. Ex vivo current clamp recordings also indicate they are resistant to firing. To elucidate their afferent control, we next used rabies tracing with whole brain imaging and channelrhodopsin-assisted circuit mapping, finding that BNST(PKCδ) cells receive abundant input from affective, arousal, and sensory regions including the basolateral amygdala (BLA), paraventricular thalamus (PVT), and central amygdala PKCδ-expressing cells (CeA(PKCδ)). Given these findings, we used in vivo optogenetics and fiber photometry to further examine BNST(PKCδ) cells in the context of stress and anxiety-like behavior. We found that BNST(PKCδ) cell activity is associated with increased anxiety-like behavior in the elevated plus maze, increases following footshock, and unlike other BNST subpopulations, doesn’t desensitize to repeated stress exposure. Taken together, we propose a model in which BNST(PKCδ) cells may serve as threat detectors, integrating exteroceptive and interoceptive information to inform stress coping behaviors. | |
