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Stowers scientists discover potential new cell types in a unique part of the nose that gives some animals scent-detecting “superpowers”

The discovery helps provide a greater understanding of the breadth of cell types governing the sense of smell.

05 December 2024

Composite cross section of a mouse vomeronasal organ with individual neurons labeled using spatial transcriptomics data.

By Rachel Scanza, Ph.D.

Service dogs not only help people navigate their surroundings but also can “smell” impending epileptic seizures, detect diseases like cancer, and even help solve crime. But how do they do it? Researchers at the Stowers Institute for Medical Research have mapped out the cells in a special sensory organ that gives certain animals like dogs their extraordinary sense of smell.

New research from the lab of former Stowers Investigator Ron Yu, Ph.D., now Chair of Neurosciences at Case Western Reserve University, has created a comprehensive atlas-like map of cells within an organ of the accessory olfactory system responsible for detecting scents beyond what humans can sense. The findings, published in eLife on November 7, 2024, reveal the spatial distribution, gene expression, and how gene expression changes throughout development of different cell types, including a previously unidentified class of cells in this accessory olfactory organ, the vomeronasal organ.

“The vomeronasal organ, which is found in most land animals, detects pheromones and other species-specific chemical cues,” said Max Hills, a bioinformatics specialist at the Institute and lead author on the study. “Studying the organ’s development and circuitry may provide clues for how sensory detection, mental state, and animal behaviors are organized.”

Distribution of the activity of nine genes across a slice of the mouse vomeronasal organ (right) and magnified expression distributions (left).

The researchers examined the vomeronasal organ of juvenile and adult mice at the single-cell level. They discovered a potential novel class of cells and, surprisingly, some neurons usually found in the main olfactory system. The study highlights the cellular and molecular complexities of this organ and its neuronal circuitry that could expand our understanding of how sensory information is processed in humans.

Located near the base of the nose, the vomeronasal organ has an unusual name—vomer refers to a triangular-shaped bone between the nose and mouth derived from the Latin word for the blade of a plow. Though not functional in humans, the vomeronasal organ’s sensory neurons detect pheromones and other chemical cues that provide crucial environmental information that can influence behaviors, such as finding potential mates or fleeing from predators.

Sensory neurons express receptor proteins on their surface, which are specific for different odor molecules—the human nose has around 400, the dog nose has over 1,000. Sensory neurons then send signals to other neurons for additional information processing. Typically, the sensory neuron to receptor connection follows a one-to-one rule, where each neuron displays a single receptor type, so that signals and responses can be very specific and trigger an appropriate reaction.

Spatial location of individual mouse vomeronasal organ cells color-coded by cell type.

While vomeronasal and olfactory sensory neurons have different roles—pheromones and innate behavior versus odors and learned behavior—the team discovered potential new types of cells in the vomeronasal organ that have both kinds of receptors. These findings suggest that the main and accessory olfactory sensory systems overlap in more complex ways than previously recognized. In addition, the researchers found a co-expression of receptors, meaning a single neuron can express several different types of receptors simultaneously.

If you have ever wondered whether our four-legged friends have an extra sense, the vomeronasal organ is a likely source. And while humans lack this extra scent sensor, untangling sensory system circuitry may reveal parallels for how odors can induce our own emotions and behaviors.

Additional authors include Limei Ma, Ph.D., Ai Fang, Ph.D., Thelma Chiremba, Ph.D., Seth Malloy, Allison Scott, and Anoja Perera.

This work was funded by the National Institute on Deafness and Other Communication Disorders of the National Institutes of Health (NIH) (awards: R01DC008003, R01DC020368) and by institutional support from the Stowers Institute of Medical Research. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.

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