Thermoregulation: How a brain keeps its cool
Keeping body temperature within a certain range is essential for nearly all animals. Endothermic animals can generate their own heat and maintain a fixed body temperature, even when the temperature of their environment changes. Nevertheless, their core body temperature fluctuates modestly but predictably throughout the day, due to programmed changes in heat production and loss (Kräuchi and Wirz-Justice, 1994). In humans, for example, the core body temperature is lowest late at night (Aschoff, 1983). These daily changes are driven by a central circadian clock in the brain and they serve as important signals, both to synchronize other circadian clocks throughout the body (Buhr et al., 2010) and to ensure that we sleep at night (Kräuchi and Wirz-Justice, 2001).
Ectothermic animals, on the other hand, cannot produce their own heat, so their body temperature is determined by their environment. However, they have evolved different strategies to regulate their temperature. Iguanas, for example, vary their daily temperature by changing their level of activity throughout the day and also by moving around to take advantage of the different ambient temperatures within their environment (Tosini and Menaker, 1995). Thus, daily variations and rhythms in body temperature can be found in both endothermic and ectothermic animals, suggesting that they are a fundamental adaptation to life on a revolving planet.
Now, in eLife, Fumika Hamada and colleagues – including Xin Tang of Cincinnati Children’s Hospital Medical Center as first author – report new insights into the regulation of body temperature in the fruit fly Drosophila melanogaster (Tang et al., 2017). Previous work from the Hamada lab established that D. melanogaster, which is ectothermic, has a daily temperature preference rhythm. By switching its preference from higher temperatures during the day to lower temperatures at night, it produces daily body temperature rhythms similar to those seen in endothermic animals (Kaneko et al., 2012).
Drosophila has a relatively simple network of approximately 150 circadian clock neurons that are organized into distinct groups (Nitabach and Taghert, 2008). Each neuron has its own circadian clock, and together they form a network that serves as the master circadian pacemaker in the fly. The Hamada lab has previously shown that a small class of clock neurons, the dorsal neuron 2 group (or DN2s for short), regulate the temperature preference rhythm in the fly (Kaneko et al., 2012). Based on these findings, Tang et al. sought to identify the underlying neural pathways.
First, they revealed that a group of neurons called small ventral lateral clock neurons, which drive the fly’s pre-dawn bout of activity (Renn et al., 1999; Stoleru et al., 2004; Grima et al., 2004), are also required for setting the temperature preference in the hours preceding dawn. When these ventral lateral neurons were disrupted, the flies preferred abnormally low temperatures just before dawn. By contrast, when DN2s were disrupted, the flies preferred lower temperatures throughout their entire 24 hour-circadian cycle.
Tang et al. then examined whether these two groups of neurons are connected and, if so, how connections change during the course of the circadian cycle. They discovered that the projections of the ventral lateral neurons terminate next to those of the DN2s and that ventral lateral neurons excite the DN2s. The number of the neural connections between the two groups of neurons increased significantly throughout the night, peaking just before dawn and falling throughout the day. This suggests that the previously discovered morphological modifications of the ventral lateral neurons, such as the expansion and contraction of their axon terminals (Fernández et al., 2008), may cause the changes in thermal preference over the course of the day.
The researchers – who are based in Cincinnati, London and Japan – next addressed how external temperature and time of day are integrated in the brain to produce a temperature preference rhythm. This was guided by previous work, which had established that a group of neurons in the central brain called anterior cell neurons act as internal heat sensors (Hamada et al., 2008). Now, Tang et al. provide compelling evidence that these anterior cells modulate the ventral lateral neurons to regulate temperature preference before dawn; when the anterior cells were blocked, the fly’s preferred temperature was lowered. Thus, they have revealed a simple neural circuitry that drives the fly’s temperature preference rhythm. Within this network, the temperature-sensing anterior cells modulate ventral lateral neurons, which in turn activate the DN2s to elevate the preferred temperature before dawn.
The fly can use daily changes in the surrounding temperature as a cue to adjust its near 24-hour endogenous period and sleep-activity cycle to match the precise 24-hour light-dark cycle (Wheeler et al., 1993). Remarkably, the temperature-sensitive pathway implicated by Tang et al. does not appear to help adjust the central clock to daily temperature cycles. Thus, Drosophila seems to rely on distinct temperature-sensing pathways to produce and adjust to daily temperature rhythms.
By identifying the neural pathways underlying the daily regulation of temperature preference, Tang, Hamada and colleagues have revealed how the fly’s brain can generate a predictable daily body temperature rhythm – a remarkable feat for a such a small ‘thermoconformer’ that constantly has to face unpredictable temperature changes.
References
-
Circadian control of body temperatureJournal of Thermal Biology 8:143–147.https://doi.org/10.1016/0306-4565(83)90094-3
-
Circadian rhythm of heat production, heart rate, and skin and core temperature under unmasking conditions in menAmerican Journal of Physiology 267:819–829.
-
Circadian clues to sleep onset mechanismsNeuropsychopharmacology 25:S92–S96.https://doi.org/10.1016/S0893-133X(01)00315-3
-
Organization of the Drosophila circadian control circuitCurrent Biology 18:R84–R93.https://doi.org/10.1016/j.cub.2007.11.061
-
Circadian rhythm of body temperature in an ectotherm (Iguana iguana)Journal of Biological Rhythms 10:248–255.https://doi.org/10.1177/074873049501000307
-
Behavior in light-dark cycles of Drosophila mutants that are arrhythmic, blind, or bothJournal of Biological Rhythms 8:67–94.https://doi.org/10.1177/074873049300800106
Article and author information
Author details
Publication history
Copyright
© 2017, Yadlapalli et al.
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
Metrics
-
- 2,391
- views
-
- 230
- downloads
-
- 1
- citations
Views, downloads and citations are aggregated across all versions of this paper published by eLife.
Download links
Downloads (link to download the article as PDF)
Open citations (links to open the citations from this article in various online reference manager services)
Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)
Further reading
-
- Neuroscience
Dense core vesicles (DCVs) transport and release various neuropeptides and neurotrophins that control diverse brain functions, but the DCV secretory pathway remains poorly understood. Here, we tested a prediction emerging from invertebrate studies about the crucial role of the intracellular trafficking GTPase Rab10, by assessing DCV exocytosis at single-cell resolution upon acute Rab10 depletion in mature mouse hippocampal neurons, to circumvent potential confounding effects of Rab10’s established role in neurite outgrowth. We observed a significant inhibition of DCV exocytosis in Rab10-depleted neurons, whereas synaptic vesicle exocytosis was unaffected. However, rather than a direct involvement in DCV trafficking, this effect was attributed to two ER-dependent processes, ER-regulated intracellular Ca2+ dynamics, and protein synthesis. Gene Ontology analysis of differentially expressed proteins upon Rab10 depletion identified substantial alterations in synaptic and ER/ribosomal proteins, including the Ca2+ pump SERCA2. In addition, ER morphology and dynamics were altered, ER Ca2+ levels were depleted, and Ca2+ homeostasis was impaired in Rab10-depleted neurons. However, Ca2+ entry using a Ca2+ ionophore still triggered less DCV exocytosis. Instead, leucine supplementation, which enhances protein synthesis, largely rescued DCV exocytosis deficiency. We conclude that Rab10 is required for neuropeptide release by maintaining Ca2+ dynamics and regulating protein synthesis. Furthermore, DCV exocytosis appeared more dependent on (acute) protein synthesis than synaptic vesicle exocytosis.
-
- Neuroscience
By influencing calcium homeostasis, local protein synthesis and the endoplasmic reticulum, a small protein called Rab10 emerges as a crucial cytoplasmic regulator of neuropeptide secretion.