The nervous and immune systems have long been thought to be separate entities in the body, but new research has uncovered a direct cellular interaction between the two. Scientists from Harvard Medical School, the Broad Institute of MIT and Harvard, MIT, and the Ragon Institute of MGH, MIT and Harvard have found that pain-sensing neurons surround lymph nodes in mice, and can modulate the activity of these small organs, which are key parts of the immune system.
The new research, published in Cell, reveals the cells that mediate the crosstalk between the nervous and immune systems. It also paves the way for more research on how the nervous system regulates immune responses, for example, during an infection.
“Once you begin to understand how these systems are structured and what are the mechanisms by which they perform their biological handshakes, it really opens up some tremendous opportunities to think about how to rationally modulate those interactions as a possible therapeutic strategy,” said Alex Shalek, co-senior author of the study, a Broad institute member, a Ragon member, and an associate professor of chemistry, a core member of the Institute for Medical Engineering and Science, and an extramural member of the Koch Institute for Integrative Cancer Research at MIT.
Ulrich von Andrian, a professor of immunopathology at Harvard Medical School and a program leader at the Ragon Institute, is co-senior author of the study. Siyi Huang, a postdoctoral fellow in von Andrian’s lab, is a co-first author of the paper.
Illuminating the lymph node
Previous research had pointed to a possible connection between neurons and lymph nodes. In the new study, the research team used a variety of methods, including advanced imaging, retrograde tracing, single-cell RNA sequencing, and optogenetics, to map the connections between neurons, immune and other types of cells within lymph nodes in mice. They found that sensory neurons that originate in a region of the spinal cord called the dorsal root ganglion formed a mesh that innervated, or made connections, throughout the periphery of the lymph node.
Out of the thousands of sensory cells in the dorsal root ganglion, the group identified only a handful that contribute to this coupling in a single lymph node. “We found the 20 or so needles in a haystack that are innervating a lymph node,” said Carly Ziegler, a graduate student with Harvard University and MIT who is in Shalek’s lab and is a co-first author of the study. “Identifying and picking out that specific cell body in a diverse set of neurons was really challenging.”
By using single-cell RNA sequencing to analyze the gene expression of these sensory cells, the team discovered that the cells were mainly pain-sensing neurons. Further analysis revealed that these neurons were highly diverse in the genes they expressed, and that they expressed different synaptic proteins and cell surface molecules than sensory neurons that innervate the skin, suggesting different modes of cell-to-cell communication.
To confirm whether the neurons were interacting with the lymph node, the researchers induced artificial immune responses in the mice and found that the pain-sensing neurons responded by increasing their density within the enlarging lymph node. This suggests that the sensory neurons can sense and effectively respond to changes in the lymph node.
The scientists also found that this communication was two-way: the neurons themselves can modulate cells in the lymph node. The researchers used optogenetics to activate these neurons and observed gene expression changes in specific cells of the lymph node, including endothelial cells.
The finding indicates that these neurons are not mere spectators. “We found that they actually can change a lot of the local environment of the lymph node and seem to be specifically influencing particular cells and structures,” said Ziegler.
The researchers are continuing to learn more about the role of these neurons in the lymph nodes, such as which mechanisms they are using to interact with the lymph nodes, whether they are mobilizing specific parts of the immune system, and what happens if these cellular circuits are lacking or dysfunctional.
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