Opioid and Pheromone: Functional Crosstalk for Stress Avoidance in C. elegans

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Introduction  

When animals encounter environmental stresses such as starvation, heat and some physical insults during their life, they can exercise various tactics to adapt to or to avoid the insults. For example, when model animal C. elegans larvae sense starvation, first, they use the opioid-like signaling system (e.g., NLP-24) to temporarily stimulate pharyngeal pumping to find food by roaming1. If starvation persists, they may use pheromones (e.g., daumones or ascarosides)2,3  as a means to warn each other such adverse situation and to induce entry into the dauer stage that allows extended survival2,3. When the situation improves, they can exit the dauer stage and continue development from the L4 stage to complete their normal life cycle. However, it remains elusive about the way of coordination between two anti-stress signals, opioids and pheromones, to facilitate their survival efforts.

Motivation and Outputs

We had been highly motivated to begin this project -Crosstalk between Opioid and Pheromones- when Mi Choong Cheong, one of our colleagues reported identification of the nematode opioid-like ligand and its receptor in 20151. Because opioid and pheromone signals both originate in the same chemosensory neurons (e.g., ASI), our group at the Paik’s lab in Yonsei University hypothesized that there should be a way of how two seemingly opposite anti-stress signaling pathways are programmed and integrated to promote the worms’ transition into the stable resting dauer state during long-term starvation stress. We have now tested this hypothesis through a series of experiments, and showed that these two signaling pathways can be integrated into one pathway that favors dauer entry under long-term starvation during their early life (L1 and L2 stages).

That is, under short-term starvation, NPR-17 opioid receptor and its related signaling autonomously overexpressed opioid genes disturbed dauer formation (Figure 1). Likewise, both long-term starvation and stress-activated pheromones negatively modulated opioid gene expression in the chemosensory neurons, which then consequently enhanced dauer formation (Figure 1). Both insulin and serotonin stimulated opioid signaling, whereas antioxidant protein and nuclear hormone receptor suppressed opioid signaling. Moreover, G-proteins alpha (GPA-3) and an antioxidant protein are proposed to regulate cross-antagonistic interaction between opioids and pheromones in a cell-specific manner, leading to long-term stable resting dauer state. The nature of the interaction between these two signaling pathways appears to be “cross-antagonistic” in which several key metabolic regulators (e.g., insulin, serotonin, TGF-β) of chemosensory processes and anti-oxidation (e.g., SKN-1) are actively interlinked.  

Figure 1. Even in a simple nematode species, individual animals can recognize starvation stress and then use stage-dependent signaling, which involves crosstalk between opioid and pheromone signaling. This novel molecular interaction between two anti-stress signals appears to be intertwined with several other signaling pathways, which culminates in stress avoidance in response to different lengths of stress exposure in early C. elegans larvae.

Scientific Impact  

To the best of our knowledge, this is the first report of a crosstalk between two anti-stress signals—opioids and pheromones—that facilitate stress avoidance in response to different durations of starvation in early stage C. elegans larvae. Mechanistically, these regulatory functions are suggested to be exerted via the selective interaction of GPA-3 with NPR-17 opioid receptor and site-specific SKN-1 binding to the promoter of nlp-24 to facilitate stress avoidance. This deserves further validation. 

Potential Clinical Implications

Because the nematode C. elegans offers many advantages as a model organism for the study of neurobiology and neurodegenerative diseases, our current work suggests the usefulness of opioid-overexpressing transgenic C. elegans strains for studying opioid overdose. These animals could potentially mimic the opioid overdose conditions that occur in human which cause nearly 70,000 deaths per year in the United States. It could thus be feasible to test the validity of such a model by measuring the effects of pretreatment with pheromone or pheromone mimetics on opioid preference in opioid-overexpressing animals (e.g., nlp-24 O/E, npr-17 O/E). Along this same line, we are just aware of the public announcement by the National Library of Medicine that an independent clinical trial is now underway to explore the possibility of pheromone-mediated opioid addiction treatment. It seems quite challenging project but is worth trying because it may add values to the pheromones for their medical applications to human disease, as proposed by our work. Let’s wait and see how it goes!

You can read more about our work: www.nature.com/articles/s41598-020-64567-3

References

  1. Cheong, M. C., Artyukhin, A. B., You, Y.-J. & Avery, L. An opioid-like system regulating feeding behavior in C. elegans. Elife 4, (2015).
  2. Jeong, P.-Y. et al. Chemical structure and biological activity of the Caenorhabditis elegans dauer-inducing pheromone. Nature 433, 541–545 (2005).
  3. Park, J. Y., Joo, H.-J., Park, S. & Paik, Y.-K. Ascaroside Pheromones: Chemical Biology and Pleiotropic Neuronal Functions. International Journal of Molecular Sciences 20, 3898 (2019).

 

 

Jun Young Park

Postdoctoral Researcher, Yonsei University

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