1. Huddling substates in mice facilitate dynamic changes in body temperature and are modulated by Shank3b and Trpm8 mutation.
- Author
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Landen JG, Vandendoren M, Killmer S, Bedford NL, and Nelson AC
- Subjects
- Animals, Mice, Male, Female, Mutation, Mice, Inbred C57BL, Body Temperature, Social Behavior, Behavior, Animal, Microfilament Proteins genetics, Microfilament Proteins metabolism, Mice, Knockout, TRPM Cation Channels genetics, TRPM Cation Channels metabolism, Body Temperature Regulation genetics, Nerve Tissue Proteins genetics, Nerve Tissue Proteins metabolism
- Abstract
Social thermoregulation is a means of maintaining homeostatic body temperature. While adult mice are a model organism for studying both social behavior and energy regulation, the relationship between huddling and core body temperature (Tb) is poorly understood. Here, we develop a behavioral paradigm and computational tools to identify active-huddling and quiescent-huddling as distinct thermal substates. We find that huddling is an effective thermoregulatory strategy in female but not male groups. At 23 °C (room temperature), but not 30 °C (near thermoneutrality), huddling facilitates large reductions in Tb and Tb-variance. Notably, active-huddling is associated with bidirectional changes in Tb, depending on its proximity to bouts of quiescent-huddling. Further, group-housed animals lacking the synaptic scaffolding gene Shank3b have hyperthermic Tb and spend less time huddling. In contrast, individuals lacking the cold-sensing gene Trpm8 have hypothermic Tb - a deficit that is rescued by increased huddling time. These results reveal how huddling behavior facilitates acute adjustments of Tb in a state-dependent manner., (© 2024. The Author(s).)
- Published
- 2024
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