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Molecular Identification of Rapidly Adapting Mechanoreceptors and Their Developmental Dependence on Ret Signaling
In mammals, the first step in the perception of form and texture is the activation of trigeminal or dorsal root ganglion (DRG) mechanosensory neurons, which are classified as either rapidly (RA) or slowly adapting (SA) according to their rates of adaptation to sustained stimuli. The molecular identi...
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Published in: | Neuron (Cambridge, Mass.) Mass.), 2009-12, Vol.64 (6), p.841-856 |
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description | In mammals, the first step in the perception of form and texture is the activation of trigeminal or dorsal root ganglion (DRG) mechanosensory neurons, which are classified as either rapidly (RA) or slowly adapting (SA) according to their rates of adaptation to sustained stimuli. The molecular identities and mechanisms of development of RA and SA mechanoreceptors are largely unknown. We found that the “early Ret+” DRG neurons are RA mechanoreceptors, which form Meissner corpuscles, Pacinian corpuscles, and longitudinal lanceolate endings. The central projections of these RA mechanoreceptors innervate layers III through V of the spinal cord and terminate within discrete subdomains of the dorsal column nuclei. Moreover, mice lacking Ret signaling components are devoid of Pacinian corpuscles and exhibit a dramatic disruption of RA mechanoreceptor projections to both the spinal cord and medulla. Thus, the early Ret+ neurons are RA mechanoreceptors and Ret signaling is required for the assembly of neural circuits underlying touch perception. |
doi_str_mv | 10.1016/j.neuron.2009.11.003 |
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The molecular identities and mechanisms of development of RA and SA mechanoreceptors are largely unknown. We found that the “early Ret+” DRG neurons are RA mechanoreceptors, which form Meissner corpuscles, Pacinian corpuscles, and longitudinal lanceolate endings. The central projections of these RA mechanoreceptors innervate layers III through V of the spinal cord and terminate within discrete subdomains of the dorsal column nuclei. Moreover, mice lacking Ret signaling components are devoid of Pacinian corpuscles and exhibit a dramatic disruption of RA mechanoreceptor projections to both the spinal cord and medulla. Thus, the early Ret+ neurons are RA mechanoreceptors and Ret signaling is required for the assembly of neural circuits underlying touch perception.</description><identifier>ISSN: 0896-6273</identifier><identifier>ISSN: 1097-4199</identifier><identifier>EISSN: 1097-4199</identifier><identifier>DOI: 10.1016/j.neuron.2009.11.003</identifier><identifier>PMID: 20064391</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adaptation, Physiological - physiology ; Afferent Pathways - cytology ; Afferent Pathways - embryology ; Afferent Pathways - metabolism ; Animal care ; Animals ; Axons - metabolism ; Axons - ultrastructure ; Brain-derived neurotrophic factor ; Dependence ; Ganglia, Spinal - cytology ; Ganglia, Spinal - embryology ; Ganglia, Spinal - metabolism ; Gene Expression Regulation, Developmental - genetics ; Hybridization ; Ligands ; Mechanoreceptors - cytology ; Mechanoreceptors - metabolism ; Mice ; Mice, Transgenic ; Neurons ; Pacinian Corpuscles - cytology ; Pacinian Corpuscles - metabolism ; Posterior Horn Cells - cytology ; Posterior Horn Cells - metabolism ; Proto-Oncogene Proteins c-ret - genetics ; Proto-Oncogene Proteins c-ret - metabolism ; Rodents ; Sensory Receptor Cells - cytology ; Sensory Receptor Cells - metabolism ; Signal Transduction - physiology ; Touch - physiology</subject><ispartof>Neuron (Cambridge, Mass.), 2009-12, Vol.64 (6), p.841-856</ispartof><rights>2009 Elsevier Inc.</rights><rights>2009 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Dec 24, 2009</rights><rights>2009 Elsevier Inc. 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subjects | Adaptation, Physiological - physiology Afferent Pathways - cytology Afferent Pathways - embryology Afferent Pathways - metabolism Animal care Animals Axons - metabolism Axons - ultrastructure Brain-derived neurotrophic factor Dependence Ganglia, Spinal - cytology Ganglia, Spinal - embryology Ganglia, Spinal - metabolism Gene Expression Regulation, Developmental - genetics Hybridization Ligands Mechanoreceptors - cytology Mechanoreceptors - metabolism Mice Mice, Transgenic Neurons Pacinian Corpuscles - cytology Pacinian Corpuscles - metabolism Posterior Horn Cells - cytology Posterior Horn Cells - metabolism Proto-Oncogene Proteins c-ret - genetics Proto-Oncogene Proteins c-ret - metabolism Rodents Sensory Receptor Cells - cytology Sensory Receptor Cells - metabolism Signal Transduction - physiology Touch - physiology |
title | Molecular Identification of Rapidly Adapting Mechanoreceptors and Their Developmental Dependence on Ret Signaling |
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