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Publication : Somatotopic organization of central arbors from nociceptive afferents develops independently of their intact peripheral target innervation.

First Author  Olson W Year  2018
Journal  J Comp Neurol Volume  526
Issue  18 Pages  3058-3065
PubMed ID  30225912 Mgi Jnum  J:277351
Mgi Id  MGI:6330910 Doi  10.1002/cne.24533
Citation  Olson W, et al. (2018) Somatotopic organization of central arbors from nociceptive afferents develops independently of their intact peripheral target innervation. J Comp Neurol 526(18):3058-3065
abstractText  Functionally important regions of sensory maps are overrepresented in the sensory pathways and cortex, but the underlying developmental mechanisms are not clear. In the spinal cord dorsal horn (DH), we recently showed that paw innervating Mrgprd(+) nonpeptidergic nociceptors display distinctive central arbor morphologies that well correlate with increased synapse transmission efficiency and heightened sensitivity of distal limb skin. Given that peripheral and central arbor formation of Mrgprd(+) neurons co-occurs around the time of birth, we tested whether peripheral cues from different skin areas and/or postnatal reorganization mechanisms could instruct this somatotopic difference among central arbors. We found that, while terminal outgrowth/refinement occurs during early postnatal development in both the skin and the DH, postnatal refinement of central terminals precedes that of peripheral terminals. Furthermore, we used single-cell ablation of Ret to genetically disrupt epidermal innervation of Mrgprd(+) neurons and revealed that the somatotopic difference among their central arbors was unaffected by this manipulation. Finally, we saw that region-specific Mrgprd(+) central terminal arbors are present from the earliest postnatal stages, before skin terminals are evident. In summary, we find that region-specific organization of Mrgprd(+) neuron central arbors is present shortly after initial central terminal formation, which likely develops independently of peripheral target innervation. Our data suggest that either cell-intrinsic and/or DH prepatterning mechanisms are likely to establish this somatotopic difference.
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