Singing modulates parvalbumin interneurons throughout songbird forebrain vocal control circuitry

• Published in: PloS one 2017-02, Vol.12 (2), p.e0172944-e0172944
• Main Authors: Zengin-Toktas, Yildiz, Woolley, Sarah Cushing
• Format: Article
• Language: English
• Subjects: Animals; Avian Proteins - metabolism; Basal ganglia; Biology and Life Sciences; Bird songs; Birds; Buffers; Calcium; Calcium buffering; Circuits; Communication; EGR-1 protein; Female; Females; Finches - physiology; Forebrain; Ganglia; Gene expression; Genetic aspects; Homeostasis; Interneurons; Interneurons - metabolism; Male; Males; Mammals; Medicine and Health Sciences; Modulation; Musical performances; Neural circuitry; Neurons; Neurosciences; Observations; Parvalbumin; Parvalbumins - metabolism; Physical Sciences; Plastic properties; Plasticity; Properties; Prosencephalon - cytology; Prosencephalon - physiology; Research and Analysis Methods; Singers; Singing; Social environment; Song; Song control nuclei; Songbirds; Subpopulations; Transcription factors; Vocalization, Animal - physiology; Zebra finch
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0172944

Across species, the performance of vocal signals can be modulated by the social environment. Zebra finches, for example, adjust their song performance when singing to females ('female-directed' or FD song) compared to when singing in isolation ('undirected' or UD song). These changes are salient, as females prefer the FD song over the UD song. Despite the importance of these performance changes, the neural mechanisms underlying this social modulation remain poorly understood. Previous work in finches has established that expression of the immediate early gene EGR1 is increased during singing and modulated by social context within the vocal control circuitry. Here, we examined whether particular neural subpopulations within those vocal control regions exhibit similar modulations of EGR1 expression. We compared EGR1 expression in neurons expressing parvalbumin (PV), a calcium buffer that modulates network plasticity and homeostasis, among males that performed FD song, males that produced UD song, or males that did not sing. We found that, overall, singing but not social context significantly affected EGR1 expression in PV neurons throughout the vocal control nuclei. We observed differences in EGR1 expression between two classes of PV interneurons in the basal ganglia nucleus Area X. Additionally, we found that singing altered the amount of PV expression in neurons in HVC and Area X and that distinct PV interneuron types in Area X exhibited different patterns of modulation by singing. These data indicate that throughout the vocal control circuitry the singing-related regulation of EGR1 expression in PV neurons may be less influenced by social context than in other neuron types and raise the possibility of cell-type specific differences in plasticity and calcium buffering.