Spatial, transcriptomic and epigenomic analyses link dorsal horn neurons to chronic pain genetic predisposition

Cynthia Arokiaraj, Michael Leone,Michael Kleyman,Alexander Chamessian,BaDoi N Phan, Bettega C Lopes, Vijay K Cherupally,Myung-Chul Noh, Kelly A Corrigan, Deepika Yeramosu, Michael E Franusich, Riya Podder, Sumitra Leie,Stephanie Shiers,Byungsoo Kang, Meaghan Kennedy,Richard Dum,David Lewis,Yawar Qadri,Theodore Price,Andreas Pfenning,Rebecca Seal

biorxiv(2024)

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摘要
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. ### Competing Interest Statement The authors have declared no competing interest.
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