A ligand-receptor interactome platform for discovery of pain mechanisms and therapeutic targets.

A ligand-receptor interactome platform for discovery of pain mechanisms and therapeutic targets.
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DOI:
10.1126/scisignal.abe1648
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发表时间:
2021-03-16
期刊:
影响因子:
7.3
通讯作者:
Price TJ
Price TJ
中科院分区:
生物学1区
文献类型:
--
作者:
Wangzhou A;Paige C;Neerukonda SV;Naik DK;Kume M;David ET;Dussor G;Ray PR;Price TJ

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In the peripheral nervous system, ligand-receptor interactions between cells and neurons shape sensory experience, including pain. We set out to identify the potential interactions between sensory neurons and peripheral cell types implicated in disease-associated pain. Using mouse and human RNA-sequencing datasets and computational analysis, we created interactome maps between dorsal root ganglion (DRG) sensory neurons and an array of normal cell types as well as colitis-associated glial cells, rheumatoid arthritis-associated synovial macrophages, and pancreatic tumor tissue. These maps revealed a common correlation between the abundance of heparin-binding EGF-like growth factor (HBEGF) in peripheral cells with that of its receptor EGFR (a member of the ErbB family of receptors) in DRG neurons. Subsequently, we confirmed that increased abundance of HBEGF enhanced nociception in mice, likely acting on DRG neurons through ErbB family receptors. Collectively, these interactomes highlight ligand-receptor interactions that may lead to treatments for disease-associated pain and, furthermore, reflect the complexity of cell-to-neuron signaling in chronic pain states.
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