Scalable control of mounting and attack by Esr1+ neurons in the ventromedial hypothalamus

• Published in: Nature (London) Vol. 509; no. 7502; pp. 627 - 632
• Main Authors: Lee, Hyosang, Kim, Dong-Wook, Remedios, Ryan, Anthony, Todd E., Chang, Angela, Madisen, Linda, Zeng, Hongkui, Anderson, David J.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 29.05.2014
• Subjects: 13/1; 14/19; 42/41; 631/378; 64/60; 9/74; Aggression - physiology; Animals; Estrogen Receptor alpha - metabolism; Female; Humanities and Social Sciences; Integrases - genetics; Integrases - metabolism; letter; Male; Mice; multidisciplinary; Neurons - metabolism; Optogenetics; Science; Sexual Behavior, Animal - physiology; Ventromedial Hypothalamic Nucleus - cytology; Ventromedial Hypothalamic Nucleus - physiology
• ISSN: 0028-0836; 1476-4687
• DOI: 10.1038/nature13169

Activation of Esr1 + neurons of the mouse ventromedial hypothalamus initiates graded social behavioural responses–weak activation triggers close investigation (sniffing) during a social encounter that often leads, with continued stimulation, to mounting behaviours by males towards either gender; mounting behaviour transitions to aggressive attacks with greater stimulation intensity. Hypothalamus neurons that mediate aggression In the mouse ventromedial hypothalamus, there are intermixed populations of neurons differentiated by the expression of the oestrogen receptor, Esr1. Previous work revealed that Esr1 + neurons can initiate aggressive behaviour when artificially activated. Here, David Anderson and colleagues extend those results to demonstrate a graded behavioural response to the activation of these neurons along a continuum of social behavior. Weaker activation could initiate close inspection during an encounter that could lead to mounting behaviours by males towards either gender with further stimulation. Mounting behaviour transitioned to aggressive attacks with even greater stimulation intensity. Thus, these data reveal a circuit that controls the nature of a set of social behaviors in a scalable manner based on neuronal activity levels. Social behaviours, such as aggression or mating, proceed through a series of appetitive and consummatory phases 1 that are associated with increasing levels of arousal 2 . How such escalation is encoded in the brain, and linked to behavioural action selection, remains an unsolved problem in neuroscience. The ventrolateral subdivision of the murine ventromedial hypothalamus (VMHvl) contains neurons whose activity increases during male–male and male–female social encounters. Non-cell-type-specific optogenetic activation of this region elicited attack behaviour, but not mounting 3 . We have identified a subset of VMHvl neurons marked by the oestrogen receptor 1 (Esr1), and investigated their role in male social behaviour. Optogenetic manipulations indicated that Esr1 + (but not Esr1 − ) neurons are sufficient to initiate attack, and that their activity is continuously required during ongoing agonistic behaviour. Surprisingly, weaker optogenetic activation of these neurons promoted mounting behaviour, rather than attack, towards both males and females, as well as sniffing and close investigation. Increasing photostimulation intensity could promote a transition from close investigation and mounting to attack, within a single social encounter. Importantly, time-resolved optogenetic inhibition experiments revealed requirements for Esr1 + neurons in both the appetitive (investigative) and the consummatory phases of social interactions. Combined optogenetic activation and calcium imaging experiments in vitro , as well as c-Fos analysis in vivo , indicated that increasing photostimulation intensity increases both the number of active neurons and the average level of activity per neuron. These data suggest that Esr1 + neurons in VMHvl control the progression of a social encounter from its appetitive through its consummatory phases, in a scalable manner that reflects the number or type of active neurons in the population.