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Regulation of Spontaneous Propagating Waves in the Embryonic Mouse Brainstem

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Date 2017 Jan 20
PMID 28101007
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Abstract

Spontaneous activity (SA) modulates many aspects of neural development, including neuronal phenotype, axon path-finding and synaptic connectivity. In the embryonic mouse brainstem, SA initially is recorded in isolated cells at embryonic day (E) 9.5, and 48 h later takes the form of propagating waves. The majority of these waves originate from one midline initiation zone (InZ), which is situated within the developing serotonergic raphe. InZ cells express a -type calcium channel, are depolarized, and have high membrane resistance, the combination of which allows spontaneous depolarization. Propagating events require signaling at metabotropic 5-HT receptors; a possible source could be 5-HT released by newly differentiating 5-HT neurons. At E11.5, waves propagate throughout the hindbrain, with some events crossing into the midbrain. At E12.5, lateral cells (further than 150 μm from the midline) up-regulate expression of a K channel that increases resting conductance and hyperpolarizes them, preventing the propagation of waves laterally. At the same stage, cells in the isthmus up-regulate -type calcium channels, permitting more events to cross into the midbrain, some of which form recurring loops of activity that are able to keep intracellular calcium levels high for many minutes. At E13.5, caudal hindbrain cells hyperpolarize utilizing the same K conductance, and 24 h later, at E14.5, the InZ hyperpolarizes and no longer undergoes spontaneous events. Thus, 5-HT receptor-dependent propagating waves in the embryonic brainstem are generated and propagated by regulation of membrane conductance. We discuss these mechanisms, and the possible role of this SA in neuronal development.

References
1.
Hunt P, Gust J, McCabe A, Bosma M . Primary role of the serotonergic midline system in synchronized spontaneous activity during development of the embryonic mouse hindbrain. J Neurobiol. 2006; 66(11):1239-52. DOI: 10.1002/neu.20259. View

2.
Scain A, Le Corronc H, Allain A, Muller E, Rigo J, Meyrand P . Glycine release from radial cells modulates the spontaneous activity and its propagation during early spinal cord development. J Neurosci. 2010; 30(1):390-403. PMC: 6632542. DOI: 10.1523/JNEUROSCI.2115-09.2010. View

3.
Blankenship A, Hamby A, Firl A, Vyas S, Maxeiner S, Willecke K . The role of neuronal connexins 36 and 45 in shaping spontaneous firing patterns in the developing retina. J Neurosci. 2011; 31(27):9998-10008. PMC: 3142875. DOI: 10.1523/JNEUROSCI.5640-10.2011. View

4.
Blankenship A, Feller M . Mechanisms underlying spontaneous patterned activity in developing neural circuits. Nat Rev Neurosci. 2009; 11(1):18-29. PMC: 2902252. DOI: 10.1038/nrn2759. View

5.
Hunt P, McCabe A, Bosma M . Midline serotonergic neurones contribute to widespread synchronized activity in embryonic mouse hindbrain. J Physiol. 2005; 566(Pt 3):807-19. PMC: 1464778. DOI: 10.1113/jphysiol.2005.089581. View