Sensory neuron development in mouse coccygeal vertebrae and its relationship to tail biopsies for genotyping
Document Type
Journal ArticlePublication Date
2014-02-04Keywords
AnimalsBiopsy
Female
Genotype
Mice
Mice, Inbred C57BL
Nerve Fibers
Neurogenesis
Nociceptors
Sacrococcygeal Region
Sensory Receptor Cells
Tail
Animal Structures
Developmental Biology
Developmental Neuroscience
Genetics
Neurosciences
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Show full item recordAbstract
A common method of genotyping mice is via tissue obtained from tail biopsies. However, there is no available information on the temporal development of sensory neurons in the tail and how their presence or absence might affect the age for performing tail biopsies. The goals of this study were to determine if afferent sensory neurons, and in particular nociceptive neurons, are present in the coccygeal vertebrae at or near the time of birth and if not, when they first can be visualized on or in those vertebrae. Using toluidine blue neuronal staining, transmission electron microscopy, and calcitonin-related gene peptide immunostaining, we found proximal to distal maturation of coccygeal nerve growth in the C57BL/6J mouse. Single nerve bundles were first seen on postpartum day (PPD) 0. On PPD 3 presumptive nociceptive sensory nerve fibers were seen entering the vertebral perichondrium. Neural development continued through the last time point (PPD 7) but at no time were neural fibers seen entering the body of the vertebrae. The effect of age on the development of pain perception in the neonatal mouse is discussed.Source
PLoS One. 2014 Feb 4;9(2):e88158. doi: 10.1371/journal.pone.0088158. eCollection 2014. Link to article on publisher's siteDOI
10.1371/journal.pone.0088158Permanent Link to this Item
http://hdl.handle.net/20.500.14038/30191PubMed ID
24505409Related Resources
Link to Article in PubMedRights
© 2014 Silverman, Hendricks. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.Distribution License
http://creativecommons.org/licenses/by/4.0/ae974a485f413a2113503eed53cd6c53
10.1371/journal.pone.0088158
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Except where otherwise noted, this item's license is described as © 2014 Silverman, Hendricks. This is an open-access article distributed under the terms of the <a href="http://creativecommons.org/licenses/by/4.0/legalcode">Creative Commons Attribution License</a>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

