Abstract
Spatial and temporal cues govern the genesis of a diverse array of neurons located in the dorsal spinal cord, including dI1-dI6, dILA, and dILB subtypes, but their physiological functions are poorly understood. Here we generated a new line of conditional knock-out (CKO) mice, in which the homeobox gene Tlx3 was removed in dI5 and dILB cells. In these CKO mice, development of a subset of excitatory neurons located in laminae I and II was impaired, including itch-related GRPR-expressing neurons, PKCγ-expressing neurons, and neurons expressing three neuropeptide genes: somatostatin, preprotachykinin 1, and the gastrin-releasing peptide. These CKO mice displayed marked deficits in generating nocifensive motor behaviors evoked by a range of pain-related or itch-related stimuli. The mutants also failed to exhibit escape response evoked by dynamic mechanical stimuli but retained the ability to sense innocuous cooling and/or warm. Thus, our studies provide new insight into the ontogeny of spinal neurons processing distinct sensory modalities. © 2013 the authors.
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CITATION STYLE
Xu, Y., Lopes, C., Wende, H., Guo, Z., Cheng, L., Birchmeier, C., & Ma, Q. (2013). Ontogeny of excitatory spinal neurons processing distinct somatic sensory modalities. Journal of Neuroscience, 33(37), 14738–14748. https://doi.org/10.1523/JNEUROSCI.5512-12.2013
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