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The cellular and molecular basis of somatosensory neuron development
Open accessAbstract
Primary somatosensory neurons convey salient information about our external environment and internal state to the CNS, allowing us to detect, perceive, and react to a wide range of innocuous and noxious stimuli. Pseudo-unipolar in shape, and among the largest (longest) cells of most mammals, dorsal root ganglia (DRG) somatosensory neurons have peripheral axons that extend into skin, muscle, viscera, or bone and central axons that innervate the spinal cord and brainstem, where they synaptically engage the central somatosensory circuitry. Here, we review the diversity of mammalian DRG neuron subtypes and the intrinsic and extrinsic mechanisms that control their development. We describe classical and contemporary advances that frame our understanding of DRG neurogenesis, transcriptional specification of DRG neurons, and the establishment of morphological, physiological, and synaptic diversification across somatosensory neuron subtypes.
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“We have identified that sensory neurons in skin organoids form ganglia and fasciculated axons mimicking the architecture of a dorsal root or trigeminal ganglion/nerve in the body”
From Generation and characterization of hair-bearing skin organoids from human pluripotent stem cells (2022) · cites this paper as [44]
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Cites
Cellular and Molecular Mechanisms of Pain
Basbaum, A. I., Bautista, D. M., Scherrer, G., & Julius, D. (2009) · Cell · doi:10.1016/j.cell.2009.09.028 · Cited by 4,344
Douarin, N. M. L., & Kalcheim, C. (1999) · Cambridge University Press eBooks · doi:10.1017/cbo9780511897948 · Cited by 3,003
Molecular Architecture of the Mouse Nervous System
Zeisel, A., Hochgerner, H., Lönnerberg, P., Johnsson, A., Memic, F., van der Zwan, J., Häring, M., Braun, E., Borm, L. E., La Manno, G., et al. (2018) · Cell · doi:10.1016/j.cell.2018.06.021 · Cited by 2,552
Neurotrophin-regulated signalling pathways
Reichardt, L. F. (2006) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2006.1894 · Cited by 2,195
Unbiased classification of sensory neuron types by large-scale single-cell RNA sequencing
Usoskin, D., Furlan, A., Islam, S., Abdo, H., Lönnerberg, P., Lou, D., Hjerling-Leffler, J., Haeggström, J., Kharchenko, O., Kharchenko, P. V., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.3881 · Cited by 2,136
Abraira, V. E., & Ginty, D. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.051 · Cited by 1,648
Self-citationTrophic factors and neuronal survival
Barde, Y.-A. (1989) · Neuron · doi:10.1016/0896-6273(89)90040-8 · Cited by 1,625
An SCN9A channelopathy causes congenital inability to experience pain
Cox, J. J., Reimann, F. M., Nicholas, A. K., Thornton, G., Roberts, E., Springell, K., Karbani, G., Jafri, H., Mannan, J., Raashid, Y., et al. (2006) · Nature · doi:10.1038/nature05413 · Cited by 1,605
The origin and development of glial cells in peripheral nerves
Jessen, K. R., & Mirsky, R. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1746 · Cited by 1,354
Briscoe, J., Pierani, A., Jessell, T. M., & Ericson, J. (2000) · Cell · doi:10.1016/s0092-8674(00)80853-3 · Cited by 1,111
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Lee, J., van der Valk, W. H., Serdy, S. A., Deakin, C., Kim, J., Le, A. P., & Koehler, K. R. (2022) · Nature Protocols · doi:10.1038/s41596-022-00681-y · Cited by 132
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Pan, Q., Guo, S.-S., Chen, M., Su, X., Gao, Z., Wang, Q., Xu, T., Liu, M., & Hu, J. (2023) · Neuron · doi:10.1016/j.neuron.2023.04.032 · Cited by 73
Xu, M., Li, Z. B., Thottappillil, N., Cherief, M., Zhu, M., Xing, X., Gomez-Salazar, M. A., Rao, C., Ramesh, S., Mwirigi, J. M., et al. (2026) · Science · doi:10.1126/science.adr9608 · Cited by 49
γ-Protocadherins control synapse formation and peripheral branching of touch sensory neurons
Meltzer, S., Boulanger, K. C., Chirila, A. M., Osei-Asante, E., DeLisle, M. M., Zhang, Q., Kalish, B. T., Tasnim, A., Huey, E. L., Fuller, L. C., et al. (2023) · Neuron · doi:10.1016/j.neuron.2023.03.012 · Cited by 40
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Batchelor, V., Perry, T. A., Cader, M. Z., & Vincent, T. L. (2025) · Nature Reviews Rheumatology · doi:10.1038/s41584-025-01280-3 · Cited by 41
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Nikolenko, V. N., Shelomentseva, E. M., Tsvetkova, M. M., Abdeeva, E. I., Giller, D. B., Babayeva, J. V., Achkasov, E. E., Gavryushova, L. V., & Sinelnikov, M. Y. (2022) · Journal of Pain Research · doi:10.2147/jpr.s348324 · Cited by 34
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Dong, S., Zhao, L., Liu, J., Sha, X., Wu, Y., Liu, W., Sun, J., Su, Y., Zhuang, Z., Chen, J., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.06.023 · Cited by 33
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Kantarci, H., Elvira, P. D., Thottumkara, A. P., O’Connell, E. M., Iyer, M., Donovan, L. J., Dugan, M. Q., Ambiel, N., Granados, A. A., Zeng, H., et al. (2024) · Cell · doi:10.1016/j.cell.2024.07.033 · Cited by 34
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Sur, D., Zeng, Y., Kobayashi, H. H., Zhi, X., Goetz, M. R., Müller, C., Zavitsanou, A., Picoli, C. C., Matos, A. A. M., Pareja, J. R., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.07.017 · Cited by 31
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Dietrich, S., Song, K., Lowenstein, E. D., Riedel, L., Birchmeier, C., Gargiulo, G., & Zampieri, N. (2022) · Nature Communications · doi:10.1038/s41467-022-34589-8 · Cited by 34
PTBP1 regulates injury responses and sensory pathways in adult peripheral neurons
Alber, S., Matteo, P. D., Zdradzinski, M. D., Costa, I. D., Medzihradszky, K. F., Kawaguchi, R., Pizio, A. D., Freund, P. A., Panayotis, N., Marvaldi, L., et al. (2023) · Science Advances · doi:10.1126/sciadv.adi0286 · Cited by 25
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Serhan, N., Abdullah, N. S., Ghéziel, N., Loste, A., Ekren, R., Labit, E., Gonzalez, A., Oliva, G., Tarot, P., Petitfils, C., et al. (2025) · Nature · doi:10.1038/s41586-025-09419-8 · Cited by 30
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Cowan, Z., Green, L., Clark, T. D., Blewett, T. A., Bonville, J. D., Gagnon, T., Hoots, E. C., Kuchenmüller, L., Leeuwis, R. H. J., Acedo, J. N., et al. (2024) · Global Change Biology · doi:10.1111/gcb.17488 · Cited by 25
Liu, F., Xu, J., Liu, A., Wu, L., Wang, D., Han, Q., Zheng, T., Wang, F., Kong, Y., Li, G., et al. (2022) · Biomaterials Science · doi:10.1039/d2bm00327a · Cited by 23
Wei, Y., Han, S., Wen, J., Liao, J., Liang, J., Yu, J., Chen, X., Xiang, S., Huang, Z., & Zhang, B. (2023) · Journal of Biomedical Science · doi:10.1186/s12929-023-00909-3 · Cited by 25
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Koutsioumpa, C., Santiago, C., Jacobs, K., Lehnert, B. P., Barrera, V., Hutchinson, J. N., Schmelyun, D. P., Lehoczky, J. A., Paul, D. L., & Ginty, D. D. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.07.020 · Cited by 23
Self-citationBen-Shaanan, T. L., Knöpper, K., Duan, L., Liu, R., Taglinao, H., Xu, Y., An, J., Plikus, M. V., & Cyster, J. G. (2024) · Developmental Cell · doi:10.1016/j.devcel.2024.05.019 · Cited by 22
Wu, L., He, J., Shen, N., & Chen, S. (2024) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2024.12.013 · Cited by 22
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Heiman, M. G., & Bülow, H. E. (2024) · Genetics · doi:10.1093/genetics/iyae056 · Cited by 21
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Guo, Y., Xiang, P., Sun, X., Liu, W., Zhou, J., Yin, B., Hou, L., Qiang, B., Li, H., Shu, P., et al. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01742-2 · Cited by 17
Meltzer, S., Boulanger, K. C., Osei-Asante, E., Handler, A., Zhang, Q., Sano, C., Itohara, S., & Ginty, D. D. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2210421119 · Cited by 17
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Self-citationXing, Y., Zan, C., & Liu, L. (2023) · Frontiers in Neural Circuits · doi:10.3389/fncir.2023.1007755 · Cited by 14
Fritzsch, B., Elliott, K. L., & Yamoah, E. N. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.913480 · Cited by 14
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Fok, A., Brissette, B., Hallacy, T. M., Ahamed, H., Ho, E., Ramanathan, S., & Ringstad, N. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112452 · Cited by 11
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Zhang, Z.-X., Tian, Y., Li, S., Jing, H., Cai, J., Li, M., & Xing, G. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01797-2 · Cited by 11
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Noguri, T., Hatakeyama, D., Kitahashi, T., Oka, K., & Ito, E. (2022) · Molecular Brain · doi:10.1186/s13041-022-00927-6 · Cited by 10
Guo, Z., Ni, H., Cui, Z., Zhu, Z., Kang, J., Wang, D., & Ke, Z. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106170 · Cited by 9
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Koyanagi, M., Ogido, R., Moriya, A., Saigo, M., Ihida, S., Teranishi, T., Kawada, J., Katsuno, T., Matsubara, K., Terada, T., et al. (2024) · Cell Reports Methods · doi:10.1016/j.crmeth.2024.100835 · Cited by 9
Yang, X., Huo, N., Zhou, H., Li, S., Fang, M., & Zhou, N. (2025) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-25-00607 · Cited by 9
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Desbois, M., & Grill, B. J. (2024) · Development · doi:10.1242/dev.202945 · Cited by 8
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Ríos, A. S., Vincenti, A. P. D., Casadei, M., Aquino, J. B., Brumovsky, P. R., Paratcha, G., & Ledda, F. (2022) · Development · doi:10.1242/dev.200583 · Cited by 7
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Jinich‐Diamant, A., Albinni, B., Fishbein, J. N., Jacobson, E., Abraira, V. E., Hong, S., Korgan, A. C., Mazzieri, A. M., & Case, L. K. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106517 · Cited by 5
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Dominguez, A. L., & Clotman, F. (2024) · Cells · doi:10.3390/cells13080652 · Cited by 5
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Goktas, S. S., Kazci, Y. E., Karadogan, B., Aydın, M. Ş., Nebol, A., Turhan, M. U., Öztürk, G., & Çağavi, E. (2022) · Journal of Neuroscience Research · doi:10.1002/jnr.25150 · Cited by 5
Banik, D. D., Martin, L. J., Tang, T., Soboloff, J., Tourtellotte, W. G., & Pierchala, B. A. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2217595120 · Cited by 5
Qualls, K. A., Xie, W., Zhang, J., Lückemeyer, D. D., Lackey, S. V., Strong, J. A., & Zhang, J. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.01.024 · Cited by 6
Wang, R., Lu, Y., Zhao, J., Duan, X., Yang, C., Zhang, Z., & Huang, R. (2024) · Biophysics Reports · doi:10.52601/bpr.2024.240036 · Cited by 4
Gertz, M. A., Aras, M. A., Bart, N., Brannagan, T. H., Griffin, J. M., Kontorovich, A., & Rosen, A. M. (2025) · Annals of Medicine · doi:10.1080/07853890.2025.2536755 · Cited by 4
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George, D., Jayaraj, N. D., Ren, D., Miller, R. E., Malfait, A., Miller, R. J., & Menichella, D. M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.27.514066 · Cited by 4
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Kim, J. H., Cetinkaya‐Fisgin, A., Zahn, N., Sari, M. C., Höke, A., & Barman, I. (2024) · Advanced Biology · doi:10.1002/adbi.202400020 · Cited by 3
Qualls, K. A., Kadakia, F. K., Serafin, E. K., Lückemeyer, D. D., Davidson, S., Strong, J. A., & Zhang, J. (2025) · Anesthesia & Analgesia · doi:10.1213/ane.0000000000007133 · Cited by 3
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Muthuirulan, P., Nityanand, A., Pandit, A., & Gururajan, V. (2025) · Sensory Neuroscience · doi:10.1002/sen2.70014 · Cited by 3
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Marques, F., Chen, Y., Destain, H., Marinelli, M., & Kratsios, P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.15.654349 · Cited by 3
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Sangster, K. T., Zhang, X., Toro, D. D., Sarantopoulos, C., Moses, A. M., Mahasenan, S., Pederick, D. T., Perreault, S., Fallet‐Bianco, C., Roome, R. B., et al. (2026) · Current Biology · doi:10.1016/j.cub.2026.04.040 · Cited by 2
Dong, Y., Wang, Y., Lv, S., Dong, Z., Zhi, K., Guo, X., Li, X., Yu, R., Zhang, Y. J., Cheng, S., et al. (2026) · Advanced Science · doi:10.1002/advs.202520995 · Cited by 2
Silagi, E. S., Nduka, E., Paiz, J. H., Pazyra‐Murphy, M. F., Bhuiyan, S. A., Renthal, W. R., & Segal, R. A. (2026) · Nature Communications · doi:10.1038/s41467-026-77192-x · Cited by 2
Fernandez, A., Sarn, N., Eng, C., & Wright, K. M. (2025) · Autism Research · doi:10.1002/aur.70119 · Cited by 3
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Franck, M. C. M., Weman, H. M., Ceder, M. M., Ahemaiti, A., Henriksson, K., Bengtsson, E., Magnusson, K. A., Koning, H. K., Öhman‐Mägi, C., & Lagerström, M. C. (2024) · Pain · doi:10.1097/j.pain.0000000000003435 · Cited by 1
Tang, Y., Lin, J., Zhao, T., Sun, L., & Liu, T. (2025) · Biomaterials Science · doi:10.1039/d4bm01635a · Cited by 1
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Koh, Z. M., Arceo, R. A., Hammer, J., Chau, K., Light, S. E. W., Dolojan, A., Januszewski, M., Svara, F., & Smith, C. J. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116761 · Cited by 2
Zhang, N., Chen, H., Gao, X., Li, S., Li, X., Li, W., Liu, K., Wang, S., & Zhu, B. (2026) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl46975 · Cited by 1
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Baltar, J., Miranda, R. M., Cabral, M., Rebelo, S., Grahammer, F., Huber, T. B., Reguenga, C., & Monteiro, F. A. (2024) · Neural Development · doi:10.1186/s13064-024-00190-6 · Cited by 1
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Netanely, Y., Saba, Y., Naamneh, R., Yacoub, S., Jaber, Y., Raviv, A., Eli‐Berchoer, L., Shapiro, H., Elinav, E., Wilensky, A., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.03.647024 · Cited by 1
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Cheong, J. C., Deursen, S. V., Amador, D., Hiner, S., & Woappi, Y. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.15.699736 · Cited by 1
Горальський, Л. П., Сокульський, І. М., Колеснік, Н. Л., Павлюченко, О. В., & Shevchuk, S. (2023) · Ukrainian Journal of Natural Sciences · doi:10.35433/naturaljournal.1.2023.19-33
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Горальський, Л. П., Сокульський, І. М., Колеснік, Н. Л., Дунаєвська, О. Ф., Радзиховский, Н. Л., Gutyj, B. V., & Shevchuk, S. (2023) · Науковий вісник Львівського національного університету ветеринарної медицини та біотехнологій імені С.З. Ґжицького · doi:10.32718/nvlvet10908
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Yoshikawa, M., Matsukawa, M., Oshima, H., Ishikawa, C., Li, H., Kudo, T., Shiba, D., Shirakawa, M., Muratani, M., Takahashi, S., et al. (2023) · Frontiers in Space Technologies · doi:10.3389/frspt.2023.1162268
Metadata
- Authors
- Meltzer, S., Santiago, C., Sharma, N., & Ginty, D. D.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Ginty, David D.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2021-12
- Volume
- 109
- Issue
- 23
- Pages
- 3736-3757
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC8639614
- OpenAlex
- W3202416243
- Cited by
- 149
- References
- 199
- Citations by year
- 2026: 38 · 2025: 33 · 2024: 39 · 2023: 23 · 2022: 15 · 2021: 1
- FWCI
- 3.12
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 365 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- Israel National Road Safety Authority (5F32NS106807-03)
- National Institutes of Health (1R01 AT011447-01, R35 5R35NS097344-05)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
- Keywords
- somatosensory neurons, dorsal root ganglia, neuronal development, peripheral nervous system development, nociception
- MeSH terms
- Animals, Axons, Ganglia, Spinal, Mammals, Neurons, Spinal Cord, Neurogenesis
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