Cargando…
Transcriptional profiling of dental sensory and proprioceptive trigeminal neurons using single-cell RNA sequencing
Dental primary afferent (DPA) neurons and proprioceptive mesencephalic trigeminal nucleus (MTN) neurons, located in the trigeminal ganglion and the brainstem, respectively, are essential for controlling masticatory functions. Despite extensive transcriptomic studies on various somatosensory neurons,...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10519964/ https://www.ncbi.nlm.nih.gov/pubmed/37749100 http://dx.doi.org/10.1038/s41368-023-00246-z |
_version_ | 1785109806074298368 |
---|---|
author | Lee, Pa Reum Kim, Jihoon Rossi, Heather Lynn Chung, Sena Han, Seung Yub Kim, Junhyong Oh, Seog Bae |
author_facet | Lee, Pa Reum Kim, Jihoon Rossi, Heather Lynn Chung, Sena Han, Seung Yub Kim, Junhyong Oh, Seog Bae |
author_sort | Lee, Pa Reum |
collection | PubMed |
description | Dental primary afferent (DPA) neurons and proprioceptive mesencephalic trigeminal nucleus (MTN) neurons, located in the trigeminal ganglion and the brainstem, respectively, are essential for controlling masticatory functions. Despite extensive transcriptomic studies on various somatosensory neurons, there is still a lack of knowledge about the molecular identities of these populations due to technical challenges in their circuit-validated isolation. Here, we employed high-depth single-cell RNA sequencing (scRNA-seq) in combination with retrograde tracing in mice to identify intrinsic transcriptional features of DPA and MTN neurons. Our transcriptome analysis revealed five major types of DPA neurons with cell type-specific gene enrichment, some of which exhibit unique mechano-nociceptive properties capable of transmitting nociception in response to innocuous mechanical stimuli in the teeth. Furthermore, we discovered cellular heterogeneity within MTN neurons that potentially contribute to their responsiveness to mechanical stretch in the masseter muscle spindles. Additionally, DPA and MTN neurons represented sensory compartments with distinct molecular profiles characterized by various ion channels, receptors, neuropeptides, and mechanoreceptors. Together, our study provides new biological insights regarding the highly specialized mechanosensory functions of DPA and MTN neurons in pain and proprioception. |
format | Online Article Text |
id | pubmed-10519964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105199642023-09-27 Transcriptional profiling of dental sensory and proprioceptive trigeminal neurons using single-cell RNA sequencing Lee, Pa Reum Kim, Jihoon Rossi, Heather Lynn Chung, Sena Han, Seung Yub Kim, Junhyong Oh, Seog Bae Int J Oral Sci Article Dental primary afferent (DPA) neurons and proprioceptive mesencephalic trigeminal nucleus (MTN) neurons, located in the trigeminal ganglion and the brainstem, respectively, are essential for controlling masticatory functions. Despite extensive transcriptomic studies on various somatosensory neurons, there is still a lack of knowledge about the molecular identities of these populations due to technical challenges in their circuit-validated isolation. Here, we employed high-depth single-cell RNA sequencing (scRNA-seq) in combination with retrograde tracing in mice to identify intrinsic transcriptional features of DPA and MTN neurons. Our transcriptome analysis revealed five major types of DPA neurons with cell type-specific gene enrichment, some of which exhibit unique mechano-nociceptive properties capable of transmitting nociception in response to innocuous mechanical stimuli in the teeth. Furthermore, we discovered cellular heterogeneity within MTN neurons that potentially contribute to their responsiveness to mechanical stretch in the masseter muscle spindles. Additionally, DPA and MTN neurons represented sensory compartments with distinct molecular profiles characterized by various ion channels, receptors, neuropeptides, and mechanoreceptors. Together, our study provides new biological insights regarding the highly specialized mechanosensory functions of DPA and MTN neurons in pain and proprioception. Nature Publishing Group UK 2023-09-25 /pmc/articles/PMC10519964/ /pubmed/37749100 http://dx.doi.org/10.1038/s41368-023-00246-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lee, Pa Reum Kim, Jihoon Rossi, Heather Lynn Chung, Sena Han, Seung Yub Kim, Junhyong Oh, Seog Bae Transcriptional profiling of dental sensory and proprioceptive trigeminal neurons using single-cell RNA sequencing |
title | Transcriptional profiling of dental sensory and proprioceptive trigeminal neurons using single-cell RNA sequencing |
title_full | Transcriptional profiling of dental sensory and proprioceptive trigeminal neurons using single-cell RNA sequencing |
title_fullStr | Transcriptional profiling of dental sensory and proprioceptive trigeminal neurons using single-cell RNA sequencing |
title_full_unstemmed | Transcriptional profiling of dental sensory and proprioceptive trigeminal neurons using single-cell RNA sequencing |
title_short | Transcriptional profiling of dental sensory and proprioceptive trigeminal neurons using single-cell RNA sequencing |
title_sort | transcriptional profiling of dental sensory and proprioceptive trigeminal neurons using single-cell rna sequencing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10519964/ https://www.ncbi.nlm.nih.gov/pubmed/37749100 http://dx.doi.org/10.1038/s41368-023-00246-z |
work_keys_str_mv | AT leepareum transcriptionalprofilingofdentalsensoryandproprioceptivetrigeminalneuronsusingsinglecellrnasequencing AT kimjihoon transcriptionalprofilingofdentalsensoryandproprioceptivetrigeminalneuronsusingsinglecellrnasequencing AT rossiheatherlynn transcriptionalprofilingofdentalsensoryandproprioceptivetrigeminalneuronsusingsinglecellrnasequencing AT chungsena transcriptionalprofilingofdentalsensoryandproprioceptivetrigeminalneuronsusingsinglecellrnasequencing AT hanseungyub transcriptionalprofilingofdentalsensoryandproprioceptivetrigeminalneuronsusingsinglecellrnasequencing AT kimjunhyong transcriptionalprofilingofdentalsensoryandproprioceptivetrigeminalneuronsusingsinglecellrnasequencing AT ohseogbae transcriptionalprofilingofdentalsensoryandproprioceptivetrigeminalneuronsusingsinglecellrnasequencing |