期刊
GENE EXPRESSION PATTERNS
卷 10, 期 1, 页码 65-74出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.gep.2009.10.003
关键词
Nociceptive; Non-nociceptive; Peptidergic; TRP channels; Expression; mRNA; Neuron; In situ hybridization; Dorsal root ganglion; Nodose ganglion; Sensory nervous system; TRPM8; Immunohistochemistry; PCR
资金
- Swedish Research Council
- Swedish Brain Foundation
- Bertil Hallsten Foundation
- Linne Foundation (DBRM)
- ERC [232675]
- Karolinska Foundation
Despite the significance of transient receptor potential (TRP) channels in sensory physiology, little is known of the expression and developmental regulation of the TRPM (melastatin) subgroup in sensory neurons. In order to find out if the eight TRPM subgroup members (TRPM1-TRPM8) have a possible role in the sensory nervous system, we characterized the developmental regulation of their expression in mouse dorsal root ganglion (DRG) from embryonic (E) day 12 to adulthood. Transcripts for all channels except for TRPM1 were detected in lumbar and thoracic DRG and in nodose ganglion (NG) with distinguishable expression patterns from E12 until adult. For most channels, the expression increased from E14 to adult with the exception of TRPM5, which displayed transient high levels during embryonic and early postnatal stages. Cellular localization of TRPM8 mRNA was found only in a limited subset of very small diameter neurons distinct in size from other populations. These neurons did not bind isolectin B4 (IB4) and expressed neither the neuropeptide calcitonin gene-related peptide (CGRP) nor neurofilament (NF)200. This suggests that TRPM8(+) thermoreceptive sensory neurons fall into a separate group of very small sized neurons distinct from peptidergic and IB4(+) subtypes of sensory neurons. Our results, showing the expression and dynamic regulation of TRPM channels during development, indicate that many TRPM subfamily members could participate during nervous system development and in the adult by determining distinct physiological properties of sensory neurons. (C) 2009 Elsevier B.V. All rights reserved.
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