Spatial, transcriptomic and epigenomic analyses link dorsal horn neurons to chronic pain genetic predisposition
Cynthia Mary ArokiarajiD, Michael J. LeoneiD, Michael KleymaniD, Alexander G. ChamessianiD, Myung‐chul NohiD, BaDoi N. PhaniD, Bettega Costa LopesiD, Kelly A. Corrigan, Vijay Kiran CherupallyiD, Deepika YeramosuiD, Mike FranusichiD, Riya Podder, Sumitra Lele, Stephanie I. ShiersiD, Byungsoo Kang, Meaghan M. Kennedy NgiD, Viola Chen, Ziheng CheniD, Hansruedi MathysiD, Richard P. Dum, David A. LewisiD, Yawar Jamal QadriiD, Theodore John PriceiD, Andreas R. PfenningiD, Rebecca P. SealiD
Abstract
Key mechanisms underlying chronic pain occur within the neural circuitry of the dorsal horn. Recent genome-wide association studies (GWAS) have identified genetic variants associated with the predisposition to chronic pain. However, most of these variants lie in regulatory non-coding regions that have so far not been linked to spinal cord function. Here, we take a multi-species approach to determine whether chronic pain variants impact regulatory elements of dorsal horn neurons. We first built a more comprehensive single cell atlas; filling gaps by generating a high-quality Rhesus macaque atlas and integrating it with human and mouse. With cellular-resolution spatial transcriptomics, we mapped the laminar distributions of the resulting species-conserved neuron subtypes, uncovering an unexpected organization. Lastly, we generated a mouse single-nucleus open chromatin atlas to partition the heritability of chronic pain traits. From this, we identified strong, selective associations between specific, conserved neuron subtypes and major forms of chronic pain.
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