Classification of Canine Primary Sensory Neurons
| dc.contributor.author | Jankelunas, Leanne Noelle | en |
| dc.contributor.committeechair | Parker, Rell Lin | en |
| dc.contributor.committeemember | Rossmeisl, John H. | en |
| dc.contributor.committeemember | Bertke, Andrea S. | en |
| dc.contributor.committeemember | Cecere, Thomas Edward | en |
| dc.contributor.department | Biomedical and Veterinary Sciences | en |
| dc.date.accessioned | 2026-07-16T08:00:13Z | en |
| dc.date.available | 2026-07-16T08:00:13Z | en |
| dc.date.issued | 2026-07-15 | en |
| dc.description.abstract | Chronic pain accounts for nearly half of owner-reported canine euthanasia decisions, yet dogs remain underutilized as a large-animal model for studying pain and developing therapeutics. Here, we present a canine dorsal root ganglion (DRG) cell atlas. Our dataset comprises 3,026 neurons and 11,734 non-neuronal cells and resolves 15 neuronal subtypes that map onto A- and C-fiber classes. We further identify eight non-neuronal subtypes, including glial, vascular, and immune populations and characterize neuronal and non-neuronal expression of physiologically relevant neuropeptides, receptors, and ion channels. We identify region-specific differences in subtype composition between lumbar and sacral DRGs. Cross-species comparisons reveal that canine DRG subtypes are broadly conserved with human and mouse, while also exhibiting canine-specific and canine–human shared molecular features relevant for translation. Together, this atlas serves as a valuable resource for understanding canine sensory neurobiology, comparing DRG organization across mammals, and leveraging dogs as a translational model for pain research. | en |
| dc.description.abstractgeneral | Hypothesis/Objectives – The objective of this study was to generate an atlas of canine primary sensory neurons. We hypothesized that there would be a significant overlap in the cell types present in dog primary sensory neurons when compared to established human and rodent atlases, and the canine atlas would be a closer model to that of humans than rodents. Animals – Six dogs between the ages of one to nine. Methods – A single-cell RNA sequencing study was performed by collecting the lumbosacral dorsal root ganglia immediately postmortem from dogs who were euthanized due to non-neurologic or orthopedic causes and had no known previous history of underlying orthopedic or neurologic disease. Nuclei isolation and Single-cell RNA sequencing were then conducted on available dorsal root ganglia using the 10x Genomics Chromium Nuclei Isolation and GEM-X Single Cell 3 kits. An atlas was then generated for selected dorsal root ganglia and compared to available human and rodent atlases. Results – Atlases were generated for selected lumbar dorsal root ganglia, showcasing the expression of a variety of neuronal markers, including SNAP-25, RBFOX3, and SPARC. Additional types of neuronal supportive tissues were also able to be identified, including immune nuclei and glial nuclei. Generated atlases revealed similarities to available human and rodent models. Conclusions and Clinical Importance: This study is the first to generate an atlas evaluating the canine primary sensory neurons, expanding the fundamental anatomic knowledge that has implications for the development of more targeted analgesics and increasing the understanding of pain responses within the canine species. | en |
| dc.description.degree | Master of Science | en |
| dc.format.medium | ETD | en |
| dc.identifier.other | vt_gsexam:47492 | en |
| dc.identifier.uri | https://hdl.handle.net/10919/143660 | en |
| dc.language.iso | en | en |
| dc.publisher | Virginia Tech | en |
| dc.rights | In Copyright | en |
| dc.rights.uri | http://rightsstatements.org/vocab/InC/1.0/ | en |
| dc.subject | Dog | en |
| dc.subject | Dorsal Root Ganglia | en |
| dc.subject | Translational Research | en |
| dc.subject | Single Cell RNAseq | en |
| dc.title | Classification of Canine Primary Sensory Neurons | en |
| dc.type | Thesis | en |
| thesis.degree.discipline | Biomedical and Veterinary Sciences | en |
| thesis.degree.grantor | Virginia Polytechnic Institute and State University | en |
| thesis.degree.level | masters | en |
| thesis.degree.name | Master of Science | en |
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