- Open Access
Deconstructing pheromone-mediated behavior one layer at a time
© Sánchez-Andrade and Logan; licensee BioMed Central Ltd. 2014
- Received: 7 May 2014
- Published: 29 May 2014
The vomeronasal organ, a sensory structure within the nasal cavity of most tetrapods, detects pheromones that influence socio-sexual behavior. It has two neuronal layers, each patterned by distinct receptor sub-families coupled to different G-proteins. Work recently published in this journal found female mice with one layer genetically inactivated are deficient in a surprisingly wide range of reproductive behaviors, providing new insights into how the nose can influence the brain.
See research article: http://www.biomedcentral.com/1741-7007/12/31
- Basal Layer
- GnRH Neuron
- Vomeronasal Organ
- Accessory Olfactory Bulb
- Pheromone Signaling
Gαi2 and Gαo have been independently ablated in mice previously [7, 8]. Although both mutant lines do display abnormal behavior, the G-proteins are expressed in other tissues so the precise role of the VNO in the behavioral phenotype could not be determined. To resolve this, Oboti and colleagues applied the Cre-Lox recombinase system to delete Gαo only in cells that express olfactory marker protein (OMP). Although these genes are co-expressed in some other sensory neurons in the nose, albeit at lower levels, only those in the basal VNO layer show a significant reduction in Gαo expression .
When tested in a battery of assays, a remarkably large range of behavioral and physiological deficiencies are observed in these mice (Figure 1). For example, male urine is unable to induce estrus in adult mutant females (a phenomenon known as the Whitten effect) while juveniles fail to undergo puberty acceleration in response to male urinary cues (the Vandenbergh effect). Adult female mice also fail to adopt a characteristic mating stance when exposed to male suitors, and are unable to detect and remember male-specific non-volatile individuality cues . In addition, both mutant males and postpartum mothers display severely curtailed aggressive responses to intruders . These phenotypes are consistent with the loss of acute pheromone signaling through V2Rs (coupled to Gαo) in the basal layer of the VNO. However, similar behavioral abnormalities have been reported in Trpc2-/- mice, which have both VNO layers inactivated . Does this imply the apical layer of the VNO has no role in mediating aggressive or sexual behaviors? We consider this unlikely, as there are aggression-promoting semiochemicals in male urine that activate the V1R/Gαi2 layer exclusively . It is possible that deactivating one layer could have an indirect effect on the function of the other. However, mice lacking basal layer function do display some behavioral differences to those with the whole VNO genetically inactivated, suggesting the Gαi2 layer is at least partly functional. A more feasible explanation may be that parallel signaling through both layers is required to instruct certain behaviors. Although initially segregated, evidence suggests that circuits downstream of V1R and V2R neurons converge deeper in the brain where synergistic activation could be necessary to generate a behavioral response.
Interrupting signal transduction in the VNO appears to have consequences beyond acute pheromone detection. Trpc2-/- mice have a reduced number of neurons in the VNO, suggesting its activity is important for cellular maintenance . The basal VNO layer is also partially degenerated in conditional Gαo mutant mice, while the apical layer remains unaffected . What phenotypic impact might a reduction in the number of neurons in the basal layer have on the mice? Curiously, group-housed conditional Gαo mutant females have severely disrupted estrus cycles, suggesting the basal layer of the VNO influences reproductive physiology independent of male pheromone signaling . The mechanism through which this occurs is unclear. Gonadotropin releasing hormone (GnRH) neurons migrate from the VNO to the forebrain during early development, where they control the release of reproductive hormones. It is therefore tempting to speculate that a degenerated basal layer could interfere with GnRH neuron migration or function. However, circulating reproductive hormone levels and ovary morphology appear normal in adult mice and Trpc2-/- females, with degeneration in both VNO layers, are not reported to have irregular estrus cycles . This unexpected phenotype may hint at a more complex relationship between the VNO and reproductive physiology than previously thought.
Producing mice with other subsets of VNO neurons inactivated is becoming ever easier due to technological advances in genetic engineering . Indeed, another recent study used a sophisticated chromosome engineering approach to further functionally subdivide the V2R/Gαo layer . Members of the H2-Mv cluster, a family of non-classical class I major histocompatibility complex genes, are expressed in approximately half of the cells in the basal layer of the VNO. When these genes are deleted the pheromone sensitivity of the neurons that express them is significantly decreased, but not entirely lost . This results in both sexual and aggressive deficits even though two-thirds of the VNO remains unperturbed, further supporting a synergistic model of pheromone signaling.
Ultimately, the systematic gene targeting of over 500 V1R and V2R genes will be necessary to reveal the full extent of the behavioral logic encoded within the molecular organization of the VNO, though, even in the era of large-scale knockout mouse programs, this will be a significant undertaking . In the meantime, increasingly sensitive transcriptomic analyses are likely to reveal genes that pattern the olfactory neurons of the nose in smaller and smaller sub-divisions. Conditionally deleting these in the VNO of mice should continue to provide novel insights into the pheromone-mediated behaviors of mammals.
The authors are supported by the Wellcome Trust, grant number 098051.
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