Worms' nervous system shown to alert immune system in Stanford studies

October 13, 2008

STANFORD, Calif. -- The nervous system and the immune system have something in common. Each has evolved to react quickly to environmental cues. Because the nervous system is able to detect some of these cues - say, a characteristic odor signaling a pathogen's presence - at a distance, it sometimes can sense trouble earlier than the immune system, which has to wait until the pathogen invades the organism.

So it makes sense that the two systems might talk to one another. Stanford University School of Medicine geneticists have shown that, indeed, they do.

In a study to be published online Oct. 14 by the journal Nature Immunology, Man-Wah Tan, PhD, assistant professor of genetics and of microbiology and immunology, and postdoctoral scholar Trupti Kawli have shown that a change in the secretion patterns of nerve cells in the minuscule soil-dwelling worm, Caenorhabditis elegans, induces a change in the worm's susceptibility to a bacterial pathogen, Pseudomonas aeruginosa. In humans, P. aeruginosa is an important pathogen among cystic fibrosis patients and can cause pneumonia.

Importantly, the Stanford investigators have nailed down the connection between the two systems. They identified a particular molecule that, secreted by nerve cells, binds to receptors in the worm's gut cells. When the levels of the secreted molecule fall, this sets off a complicated chain reaction that activates the powerful immune defense against bacterial infection. Since bacteria are what C. elegans mainly eats, this is a handy defense to have.

The notion of crosstalk between our nervous and immune systems is hardly surprising, said Tan. "A person who is undergoing prolonged psychological stress - say, because they're taking care of someone who is sick - is more likely to have reactivation of a latent infection or become more susceptible to new ones," he said. "That stressful situation cannot be changed. But by identifying the pathways through which the nervous system alters immune function in this simple creature C. elegans, we can perhaps start to think about how we can intervene in humans."

The very complexity of the nervous and immune systems would make any interactions between them exceedingly tough to tease out in humans. So Kawli and Tan used C. elegans, because both its nervous and immune systems have been entirely mapped out. This enabled the researchers to manipulate the former, then watch what happened to the latter.

C. elegans has nerve cells that ordinarily secrete bioactive molecules contained within tiny membrane-wrapped bundles, called dense-core vesicles. The rate at which these molecules are secreted is governed by the activity of the nervous system. One of those secreted bioactive molecules is called ins-7. The Stanford team obtained or generated various C. elegans mutants that lacked the ability either to produce or to secrete ins-7, or secreted it excessively.

By using these and other advanced laboratory tools to manipulate the worm's ability to secrete ins-7, the researchers were able to correspondingly alter the readiness of the minuscule creature's innate immune system: a primitive but potent piece of the immune system shared by C. elegans and higher organisms including humans.

People often associate "immune response" with antibodies and roving T-cells dispatched to combat a particular viral or bacterial infection - the so-called adaptive immune response. But that response takes a week or two to develop, said Tan. In contrast, all of our cells have receptors that can recognize molecular patterns common to whole classes of pathogens (for example, characteristic viral DNA snippets, or bacterial cell-wall constituents), immediately triggering cascades of intracellular reactions, such as the activation of batteries of genes that code for antimicrobial proteins.

Both the innate and adaptive branches of the immune system have to function optimally in order for us to leave a healthy life. "The innate immune system is our first line of defense," said Tan. "If not for the innate immune system, we'd be dead by the time the adaptive immune system raises antibodies to a pathogenic invader we have not encountered before."

It is still a matter of speculation as to how crosstalk between the nervous and immune systems of humans regulates innate immune responses. But now that a clear pathway has been identified in the worm, it will be easier to conduct focused research on higher organisms to see if the phenomenon is universal, Tan said.

Tan acknowledged that it has not yet been proven that the signaling of the nervous system to the immune system of C. elegans, as shown in this experiment, occurs in nature. But there's very good reason to believe it does.

In a separate paper set to be published online on Oct. 17 by another journal, PLoS-Pathogens, Tan and other Stanford associates demonstrate that P. aeruginosa - which is often isolated from the same soil samples in which C. elegans is found and, presumably, co-evolved with C. elegans - has a way of subverting this defense against it. The pathogen induces excess production of ins-7 by the worm to dull its immune responsiveness. In contrast, other human bacterial pathogens such as Salmonella typhimurium and Enterococcus fecalis have no such capability. Nor do abiotic stresses, such as heat or heavy metals.

This suggests to Tan that the fine-tuning of the innate immune response by the nervous system is effective enough in the natural state that some pathogens with which C. elegans coexists have evolved strategies to subvert this system.

An inducible immune response makes more sense - in worms and people - than a state of constantly hyper-elevated immune vigilance. People with hyperactive immune systems suffer from autoimmune and inflammatory conditions. Although worms with downregulated secretion from dense-core vesicles are better at combating infection, they don't move well, which would probably prove lethal in the wild. One of the ins-7-deficient C. elegans mutants used in the Nature Immunology study is called unc, said Kawli, the paper's first author. "That stands for 'uncoordinated,'" she said.
-end-
Funding for the Nature Immunology study came from the National Institutes of Health.Stanford University Medical Center integrates research, medical education and patient care at its three institutions -- Stanford University School of Medicine, Stanford Hospital & Clinics and Lucile Packard Children's Hospital at Stanford. For more information, please visit the Web site of the medical center's Office of Communication & Public Affairs at http://mednews.stanford.edu.

Stanford University Medical Center

Related Immune System Articles from Brightsurf:

How the immune system remembers viruses
For a person to acquire immunity to a disease, T cells must develop into memory cells after contact with the pathogen.

How does the immune system develop in the first days of life?
Researchers highlight the anti-inflammatory response taking place after birth and designed to shield the newborn from infection.

Memory training for the immune system
The immune system will memorize the pathogen after an infection and can therefore react promptly after reinfection with the same pathogen.

Immune system may have another job -- combatting depression
An inflammatory autoimmune response within the central nervous system similar to one linked to neurodegenerative diseases such as multiple sclerosis (MS) has also been found in the spinal fluid of healthy people, according to a new Yale-led study comparing immune system cells in the spinal fluid of MS patients and healthy subjects.

COVID-19: Immune system derails
Contrary to what has been generally assumed so far, a severe course of COVID-19 does not solely result in a strong immune reaction - rather, the immune response is caught in a continuous loop of activation and inhibition.

Immune cell steroids help tumours suppress the immune system, offering new drug targets
Tumours found to evade the immune system by telling immune cells to produce immunosuppressive steroids.

Immune system -- Knocked off balance
Instead of protecting us, the immune system can sometimes go awry, as in the case of autoimmune diseases and allergies.

Too much salt weakens the immune system
A high-salt diet is not only bad for one's blood pressure, but also for the immune system.

Parkinson's and the immune system
Mutations in the Parkin gene are a common cause of hereditary forms of Parkinson's disease.

How an immune system regulator shifts the balance of immune cells
Researchers have provided new insight on the role of cyclic AMP (cAMP) in regulating the immune response.

Read More: Immune System News and Immune System Current Events
Brightsurf.com is a participant in the Amazon Services LLC Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon.com.