Coexpression of Runx1 and Runx3 in mechanoreceptive dorsal root ganglion neurons.

Dev Neurobiol

Doctoral Program in Kansei, Behavioral and Brain Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Ibaraki, 305-8577, Japan.

Published: June 2013

AI Article Synopsis

  • Runx transcription factors (Runx1 and Runx3) play crucial roles in cell development, specifically in distinct populations of sensory neurons in the dorsal root ganglion (DRG), impacting nociceptive and proprioceptive neuron differentiation.
  • During the study of mice, it was found that Runx3 expression occurs earlier than Runx1, but declines significantly before birth, while Runx1 continues to be expressed during postnatal development.
  • Additionally, some neurons express both Runx1 and Runx3 throughout development, and their coexpression, along with other receptors, suggests these neurons may be involved in mechanoreceptive functions in the DRG.

Article Abstract

Runt-related transcription factors (Runx) regulate the development of various cells. It has been reported that Runx1 and Runx3 are expressed in distinct subpopulations of primary sensory neurons in the dorsal root ganglion (DRG), and play important roles in the differentiation of nociceptive and proprioceptive neurons, respectively. In the present study, we examined the developmental changes of the expression of Runx1 and Runx3 in the mouse DRG during embryonic and postnatal stages. We found that the expression of Runx3 preceded that of Runx1, but dramatically decreased before birth, whereas the Runx1 expression was maintained during postnatal periods. These results suggest that roles of Runx1 and Runx3 may change dynamically in the differentiation and maturation of DRG neurons. In addition, several DRG neurons expressed both Runx1 and Runx3 throughout embryonic and postnatal stages and many Runx3-expressing DRG neurons coexpressed Runx1 at postnatal day 28. Double and triple labeling studies suggest that some of the Runx1/Runx3-double expressing neurons coexpressed TrkB, c-ret, and TrkC, which have been shown in the mechanoreceptive DRG neurons. These results suggest that Runx1/Runx3-double expressing neurons may represent mechanoreceptive properties in the DRG.

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Source
http://dx.doi.org/10.1002/dneu.22073DOI Listing

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