Making sense out of spinal cord somatosensory development
Open accessAbstract
The spinal cord integrates and relays somatosensory input, leading to complex motor responses. Research over the past couple of decades has identified transcription factor networks that function during development to define and instruct the generation of diverse neuronal populations within the spinal cord. A number of studies have now started to connect these developmentally defined populations with their roles in somatosensory circuits. Here, we review our current understanding of how neuronal diversity in the dorsal spinal cord is generated and we discuss the logic underlying how these neurons form the basis of somatosensory circuits.
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Post-mitotic neurons in the spinal cord do not appear to maintain laminar organization at later stages.
“Whereas spinal cord progenitors are organized in a well-defined laminar pattern during development, post-mitotic neurons in the spinal cord do not appear to maintain this organization at later stages”
From Generation of Functional Human 3D Cortico-Motor Assembloids (2020) · cites this paper as Lai et al., 2016
The decrease in dorsal progenitors at e13.5 is in line with the higher rate of neurogenesis in the dorsal spinal cord at e13.5 and the consequent depletion of progenitors.
“This is in line with the higher rate of neurogenesis in the dorsal spinal cord at e13.5 and the consequent depletion of progenitors”
From Single cell transcriptomics reveals spatial and temporal dynamics of gene expression in the developing mouse spinal cord (2019) · cites this paper as Lai et al., 2016
Differentiation of dp1-dp3 progenitors into dI1-dI3 neurons depends on expression of proneural bHLH proteins: Atoh1 in dp1; Neurog1 in dp2; and Neurog2 in dp2 and dp3 progenitors.
“Differentiation of these progenitors into dI1-dI3 neurons depends on the expression of the proneural bHLH proteins: Atoh1 in dp1; Neurog1 in dp2; and Neurog2 in dp2 and dp3 progenitors (Lai et al., 2016).”
From Single cell transcriptomics reveals spatial and temporal dynamics of gene expression in the developing mouse spinal cord (2019) · cites this paper as Lai et al., 2016
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- Authors
- Lai, H. C., Seal, R. P., & Johnson, J. E.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- University of Pittsburgh (US)
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2016-10-01
- Volume
- 143
- Issue
- 19
- Pages
- 3434-3448
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- PMC
- PMC5087618
- OpenAlex
- W2528052116
- Cited by
- 188
- References
- 181
- Citations by year
- 2026: 13 · 2025: 15 · 2024: 17 · 2023: 18 · 2022: 23 · 2021: 33 · 2020: 21 · 2019: 23 · 2018: 13 · 2017: 11 · 2015: 1
- FWCI
- 1.95
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Development (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- National Institutes of Health (R01 HD037932, R01 NS032817)
- Rita Allen Foundation
- American Pain Society
- 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 › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Keywords
- spinal cord development, neuronal heterogeneity, transcriptional regulatory networks, neuronal specification, sensory integration, motor control
- MeSH terms
- Animals, Humans, Interneurons, Models, Theoretical, Neurons, Sensation, Spinal Cord, Transcription Factors
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