Dan Berkowitz might never have noticed the phenomenon if not for the new lights. In 2012, Johns Hopkins University’s Berkowitz had just moved to a lab space where the lights were motion-activated, and his postdoc Gautam Sikka soon began to observe a curious response in the blood vessels he had isolated for study: whenever he walked in and the lights turned on, the vessels exerted less pressure on the force transducer the researchers had attached to constantly stream data.
A literature search revealed that the relaxation of blood vessels in response to light, called photorelaxation, had been described almost 50 years earlier, but the underlying mechanisms had never been fully elucidated. Berkowitz wondered if these effects were mediated by resident light-sensing pigments. If so, it wouldn’t be the first time that a sensory receptor had been found outside of a sense organ.
The light, odor, and taste receptors located in our eyes, noses, and tongues flood our brain with information about the world around us. But these same sensory receptors are also present in unexpected places around the body, where they serve a surprising range of biological roles. In the last decade or so, researchers have found that the gut “tastes” parasites before initiating immune responses, and the kidneys “smell” fatty acids, regulating blood pressure in response. Sure enough, upon further investigation Berkowitz found that it was melanopsin, a light-sensing pigment that serves circadian entrainment and other nonvisual functions in the eye, that modulated the relaxation of blood vessels when the lab lights came on.
In contrast to the early days of the field, the idea of sensory receptors outside of sensory organs is no longer unusual. “They’re all just chemoreceptors, and you can use them in lots of different contexts in physiologically different systems,” says University of Colorado Denver neurobiologist Thomas Finger.
Now researchers are characterizing such sense receptors present in different tissues around the body and working to understand their functions, with the eventual goal of using these receptors for various diagnostic or therapeutic applications. Preliminary trials are underway to test therapeutic uses of light-induced vasodilation in humans, for example, and clinical trials will soon test whether a patient’s taste receptors—both those in the mouth and those in the airway—could be used to diagnose and to treat respiratory infections, respectively. While many of the details of the receptors’ activation and downstream signaling remain unclear, researchers are finally getting closer to making sense of what these receptors do outside of the classic sense organs. And labs are using modern genetic tools, such as arrays to detect gene expression or protein levels in different tissues, to pin them down.
“Now, people are looking for them,” says Jennifer Pluznick of Johns Hopkins University. “If it comes up in an array, people are more likely to say, ‘Oh, this could be interesting,’ rather than, ‘This is meaningless.’”
Follow that smell
Intrigued, Hanns Hatt of Ruhr-University Bochum decided to look for these receptors in human sperm. “We could indeed show that such olfactory receptor genes are expressed in human sperm cells also, and a couple of olfactory receptor proteins could be detected,” says Hatt. In 2003, Hatt and his colleagues showed that olfactory receptors in human sperm were functional and could be activated by an odor molecule, just like the receptors in the nose.4 Still, the findings were met with resistance from the field, Hatt says. “At the beginning it was really hard to convince my scientific colleagues that these olfactory receptors are not expressed exclusively in the nose.”
Over the next decade, Hatt’s team and others continued to identify olfactory receptors in a variety of human tissues, including the lungs, liver, skin, heart, and intestines. In fact, they are some of the most highly expressed genes in many tissues. “One can be sure that these receptors must have enormous importance for the cell,” Hatt says.
Now, the looming question is: What are these receptors doing? “The big problem is that, to study the function of olfactory receptor proteins, one has to know how you can activate the receptor,” says Hatt. Humans have some 350 types of functional olfactory receptors (mice and rats have about 1,000), and researchers have only identified the activating odor molecules for 10 percent to 20 percent of them. To find out what activates a particular receptor, Hatt expresses its gene in a human cell line and exposes the cells to a panel of a few hundred to a few thousand different odor molecules, typically commercially available artificial scents such as those used for perfumes or other cosmetic products.
Hatt also found that an artificial sandalwood scent called sandalore activates an olfactory receptor in skin. Activating this receptor stimulated skin cells to migrate and proliferate more rapidly, leading to faster regeneration and wound healing.5 Again, the receptor’s natural ligand—likely a chemical or hormone with a similar structure to sandalore—remains to be determined.
Some olfactory receptors have similar functions in different tissues. In 2009, Emory University’s Grace Pavlath was studying how muscle cells fuse to form multinucleated fibers when she noticed high expression levels for the same olfactory receptor Hatt had found in sperm. She found that this olfactory receptor attracts muscle cells toward a particular scent, thus directing muscle migration. “It makes absolute sense that you would use it as a ‘tractor beam’ to tell cells where to go,” Pavlath says. Without this receptor, muscle fibers in mice are more prone to injury and regenerate poorly, whereas overexpressing this receptor improves regeneration.6,7 Finding the receptor’s natural ligand “would allow you potentially to design drugs that could activate this receptor and enhance muscle regeneration,” says Pavlath.
In a few cases, researchers may have identified the natural ligands responsible for activating olfactory receptors around the body. In the kidney, for example, Johns Hopkins University’s Pluznick found that certain short-chain fatty acids produced by gut bacteria can activate olfactory receptor 78 (Olfr78), which in mice triggers changes in blood pressure. When researchers injected mice lacking the gene for Olfr78 with short-chain fatty acids, the animals’ blood pressure dropped, suggesting that Olfr78 by itself normally increases blood pressure in response to the compounds. But blood pressure regulation is complicated, and Pluznick found another, nonolfactory receptor called Gpr41 that decreased blood pressure in response to short-chain fatty acids and had a stronger effect than Olfr78.8 Pluznick suggests that the two receptors might act together to produce a buffering effect that protects against wild swings in blood pressure as fatty-acid levels fluctuate.
“There are hints in the literature that things that you would expect to increase short-chain fatty production are associated with changes in blood pressure,” says Pluznick. Gut bacteria produce short-chain fatty acids when the microbes digest foods rich in fiber, for example, and eating more fiber has been associated with lower blood pressure. One could imagine, then, that eating fibrous foods, or ingesting probiotics, might help regulate blood pressure, Pluznick adds. “That’s obviously a long-term dream goal, but I think there’s some potential excitement there.”
Misplaced olfactory receptors may also prove useful in cancer treatment. Hatt has identified olfactory receptors expressed very highly in a number of different types of cancer cells, and stimulating those receptors caused tumors to shrink in vitro.9 Although much more research is needed to be able to translate those findings into a cancer therapy, Hatt is hopeful that the field is headed in that direction. “I think it will be a huge new family of possible targets for diagnosis and therapy for different diseases,” he says.
It was only after Berkowitz switched lab spaces that it became clear to him that melanopsin wasn’t limited to the retina. After Sikka observed the relaxation of blood vessels when the automatic lights switched on, Berkowitz and his team began searching for expression of the melanopsin gene Opn4 and found that it was “quite ubiquitous throughout blood vessels,” he says. Using Opn4 knockout mice and pharmacological inhibitors, the researchers confirmed that melanopsin indeed mediated the relaxation of blood vessels in response to light.11 This photorelaxation effect was specific to the blue wavelengths of light, consistent with the pigment’s absorption spectrum. Berkowitz’s team also discovered that photorelaxation was regulated by G protein–coupled receptor kinase 2 (GRK2). While exposure to light alone could cause a 20 percent to 25 percent relaxation of blood vessels, coupling light with a GRK2 inhibitor resulted in a 75 percent to 100 percent relaxation.
Regardless of its physiological role, Berkowitz is trying to harness light-induced photorelaxation to treat vascular diseases, such as Raynaud’s phenomenon. Patients with Raynaud’s experience an extreme constriction of the blood vessels in their fingers and toes in response to cold, limiting circulation and causing these extremities to feel numb or painful. Patients could potentially wear gloves that emit blue light to improve their peripheral blood flow, Berkowitz suggests. This could “induce some relief for these patients that have terrible cold and pain and can’t pick up a glass of cold soda,” he says.
In addition, light therapy could help newborns who suffer from pulmonary hypertension—high blood pressure in the arteries of their lungs and hearts. Current drug treatments have various side effects, and “light might be a safe potential alternative,” says Berkowitz, who is currently developing techniques to sidestep the fact that blue light doesn’t penetrate very deep into the body. “Hopefully, if that technology works, we can leverage it to other diseases in which vasoconstriction is a significant problem,” he says. “Any kind of disease process in which blood vessel constriction is a problem, whether it’s diabetes, peripheral vascular disease, [or] coronary artery disease, could potentially be treated using light-based therapy.”
A taste for pathogens
Some taste receptors in the gut appear to detect nutrients from food. Others are present in mouse testes and sperm, and knocking them out renders mice infertile, although the mechanism is unknown. A number of recent reports also indicate a role for taste receptors in our body’s immune reaction to certain bacteria and parasites.
Finger initially studied the chemical senses of fish, which have sensory cells in their skin that are biochemically and structurally similar to the cells in our taste buds. In 2003, he and his colleagues showed that these cells, called solitary chemosensory cells, were also present in mammalian noses.12 The researchers identified solitary chemosensory cells expressing bitter taste receptors in the mouse upper respiratory tract and showed that molecules produced by gram-negative bacteria to communicate with each other activated these receptors and stimulated the secretion of inflammatory peptides to initiate an innate immune response.13
“It’s a really, really cool story of how the sweet and bitter receptors in this one cell, the solitary chemosensory cells, are like yin and yang,” says Cohen. “The sweet receptor is measuring how much glucose is sitting in the airway. As long as the sweet receptor is being stimulated, it inhibits activation of the bitter receptor.”
It’s a really, really cool story of how the sweet and bitter receptors in this one cell, the solitary chemosensory cells, are like yin and yang.—Noam Cohen,
University of Pennsylvania
Other upper respiratory cells have hairlike protrusions called motile cilia that serve as motors to drive mucus out of the airway, carrying bacteria and irritants with it. A team at the University of Iowa discovered that these cells also express bitter taste receptors on the cilia that can sense and respond to bacterial signaling molecules.15 Just like the bitter receptors found in the solitary chemoreceptor cells, Cohen and colleagues found, these ciliated cells’ taste receptors can stimulate the innate immune system upon binding to bacterial compounds. They also respond by increasing the speed with which the cilia beat.16
Taste receptors’ response to bacterial signals occurs within seconds or minutes, making them a first line of defense against airway pathogens, Cohen says. As a result, the type of receptors we have may affect how we react to upper respiratory infections. Cohen studied T2R38, a bitter taste receptor in ciliated cells, that is quite variable in human populations. It’s the same receptor that’s thought to make some people “super-tasters,” particularly sensitive to bitter compounds found in foods such as broccoli and brussels sprouts. Patients with the super-taster version of the receptor may be able to detect bacterial compounds at very low concentrations in the airway, Cohen suggests. The receptor “doesn’t even let bacteria get a foothold to set up any kind of colonization or infection,” he adds. Cohen and his colleagues found that patients with this version of T2R38 very rarely got gram-negative upper respiratory infections, and the type of receptor a patient possesses predicts the success of sinus surgery. When patients have chronic sinusitis that’s severe enough to require surgery, Cohen found, those who are more sensitive to bitter compounds do much better post-surgery, with fewer subsequent infections and improved breathing and sleeping compared with those who are less sensitive.
Cohen suggests that having a patient taste a variety of nontoxic chemicals to rate their bitterness could serve as a cheap and rapid diagnostic tool. “Our ultimate goal is to use this to try to determine what potential pathogens an individual could be susceptible to,” he says. Eventually, researchers may be able to take advantage of the taste receptors for therapeutic purposes, perhaps by squirting a bitter substance into the nose to stimulate an innate immune response. Cohen plans to start testing candidate therapeutic compounds in clinical trials this year. “If this works the way we think it might work, it might be the first line of therapy you get when you come in with some sort of infection,” he says.
Recent findings suggest that taste receptors may also play a critical role in immune responses in the gut. Taste receptors are expressed in certain epithelial cells in the gut, called tuft cells, and “the assumption was that this might have something to do with reacting to food,” says Harvard University’s Michael Howitt. But after seeing Finger’s and Cohen’s work, Howitt wondered if taste could also play a role in detecting microbes.
Sure enough, Howitt discovered that taste signaling by tuft cells can be activated by single-celled and roundworm parasites in the mouse gut.17 “If you think about the intestine almost as a medieval castle, the tuft cells are like the little guards posted on the various towers,” he says. “If they detect, through taste, the parasites, then they sound the alarm to the immune system.” Although the exact receptors involved remain to be discovered, Howitt found that without key taste signaling molecules, the immune system never reacts, and the gut struggles to get rid of the parasites. The findings raise the possibility “of taste not only as a way to discriminate between different foods, but that it might be broadly conserved in detecting a whole suite of different microbes,” Howitt says.
“I think it’s a very interesting couple of stories panning out about the protective uses of these receptors in taste-like cells in the gut and in the airways,” says Robert Margolskee of the Monell Center. And activating taste receptors to stimulate a person’s immune cells could hold some benefits over other treatments, says Margolskee—namely, “you wouldn’t expect to get drug-resistant bacteria.”
Many questions remain about the sensory receptors that have been identified throughout the body—in particular, what activates them and what physiological functions they serve. But with potential therapeutic applications on the horizon, “it is a field that is growing enormously,” says Ruhr-University Bochum’s Hatt. “Twenty years ago, no one was really excited by olfaction or taste. . . . That has changed dramatically.”
Sandeep Ravindran is a freelance science writer living in New York City.
- L. Buck, R. Axel. “A novel multigene family may encode odorant receptors: A molecular basis for odor recognition,” Cell, 65:175-87, 1991.
- M. Parmentier et al., “Expression of members of the putative olfactory receptor gene family in mammalian germ cells,” Nature, 355:453-55, 1992.
- P. Vanderhaeghen et al., “Olfactory receptors are displayed on dog mature sperm cells,” J Cell Biol, 123:1441-52, 1993.
- M. Spehr et al., “Identification of a testicular odorant receptor mediating human sperm chemotaxis,” Science, 299:2054-58, 2003.
- 5. D. Busse et al., “A synthetic sandalwood odorant induces wound-healing processes in human keratinocytes via the olfactory receptor OR2AT4,” J Invest Dermatol, 134:2823-32, 2014.
- C.A. Griffin et al., “MOR23 promotes muscle regeneration and regulates cell adhesion and migration,” Dev Cell, 17:649-61, 2009.
- C. Pichavant et al., “Decrease of myofiber branching via muscle-specific expression of the olfactory receptor mOR23 in dystrophic muscle leads to protection against mechanical stress,” Skelet Muscle, 6:2, 2016.
- J.L. Pluznick et al., “Olfactory receptor responding to gut microbiota–derived signals plays a role in renin secretion and blood pressure regulation,” PNAS, 110:4410-15, 2013.
- E.M. Neuhaus et al., “Activation of an olfactory receptor inhibits proliferation of prostate cancer cells,” J Biol Chem, 284:16218-25, 2009.
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- T.E. Finger at al., “Solitary chemoreceptor cells in the nasal cavity serve as sentinels of respiration,” PNAS, 100:8981-86, 2003.
- M. Tizzano et al., “Nasal chemosensory cells use bitter taste signaling to detect irritants and bacterial signals,” PNAS, 107:3210-15, 2010.
- R.J. Lee et al., “Bitter and sweet taste receptors regulate human upper respiratory innate immunity,” J Clin Invest, 124:1393-405, 2014.
- A.S. Shah et al., “Motile cilia of human airway epithelia are chemosensory,” Science, 325:1131-34, 2009.
- R.J. Lee et al., “T2R38 taste receptor polymorphisms underlie susceptibility to upper respiratory infection,” J Clin Invest, 122:4145-59, 2012.
- M.R. Howitt et al., “Tuft cells, taste-chemosensory cells, orchestrate parasite type 2 immunity in the gut,” Science, 351:1329-33, 2016.