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A DRG genetic toolkit reveals molecular, morphological, and functional diversity of somatosensory neuron subtypes.


ABSTRACT: Mechanical and thermal stimuli acting on the skin are detected by morphologically and physiologically distinct sensory neurons of the dorsal root ganglia (DRG). Achieving a holistic view of how this diverse neuronal population relays sensory information from the skin to the central nervous system (CNS) has been challenging with existing tools. Here, we used transcriptomic datasets of the mouse DRG to guide development and curation of a genetic toolkit to interrogate transcriptionally defined DRG neuron subtypes. Morphological analysis revealed unique cutaneous axon arborization areas and branching patterns of each subtype. Physiological analysis showed that subtypes exhibit distinct thresholds and ranges of responses to mechanical and/or thermal stimuli. The somatosensory neuron toolbox thus enables comprehensive phenotyping of most principal sensory neuron subtypes. Moreover, our findings support a population coding scheme in which the activation thresholds of morphologically and physiologically distinct cutaneous DRG neuron subtypes tile multiple dimensions of stimulus space.

SUBMITTER: Qi L 

PROVIDER: S-EPMC10153270 | biostudies-literature | 2023 Apr

REPOSITORIES: biostudies-literature

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A DRG genetic toolkit reveals molecular, morphological, and functional diversity of somatosensory neuron subtypes.

Qi Lijun L   Iskols Michael M   Shi David D   Reddy Pranav P   Walker Christopher C   Lezgiyeva Karina K   Voisin Tiphaine T   Pawlak Mathias M   Kuchroo Vijay K VK   Chiu Isaac I   Ginty David D DD   Sharma Nikhil N  

bioRxiv : the preprint server for biology 20230423


Mechanical and thermal stimuli acting on the skin are detected by morphologically and physiologically distinct sensory neurons of the dorsal root ganglia (DRG). Achieving a holistic view of how this diverse neuronal population relays sensory information from the skin to the central nervous system (CNS) has been challenging with existing tools. Here, we used transcriptomic datasets of the mouse DRG to guide development and curation of a genetic toolkit to interrogate transcriptionally defined DRG  ...[more]

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