Literature DB >> 29676260

Embryonic and postnatal neurogenesis produce functionally distinct subclasses of dopaminergic neuron.

Elisa Galliano1,2,3, Eleonora Franzoni1, Marine Breton1, Annisa N Chand1, Darren J Byrne1, Venkatesh N Murthy2,3, Matthew S Grubb1.   

Abstract

Most neurogenesis in the mammalian brain is completed embryonically, but in certain areas the production of neurons continues throughout postnatal life. The functional properties of mature postnatally generated neurons often match those of their embryonically produced counterparts. However, we show here that in the olfactory bulb (OB), embryonic and postnatal neurogenesis produce functionally distinct subpopulations of dopaminergic (DA) neurons. We define two subclasses of OB DA neuron by the presence or absence of a key subcellular specialisation: the axon initial segment (AIS). Large AIS-positive axon-bearing DA neurons are exclusively produced during early embryonic stages, leaving small anaxonic AIS-negative cells as the only DA subtype generated via adult neurogenesis. These populations are functionally distinct: large DA cells are more excitable, yet display weaker and - for certain long-latency or inhibitory events - more broadly tuned responses to odorant stimuli. Embryonic and postnatal neurogenesis can therefore generate distinct neuronal subclasses, placing important constraints on the functional roles of adult-born neurons in sensory processing.
© 2018, Galliano et al.

Entities:  

Keywords:  axon initial segment; development; dopamine; mouse; neurogenesis; neuroscience; olfactory bulb

Mesh:

Year:  2018        PMID: 29676260      PMCID: PMC5935487          DOI: 10.7554/eLife.32373

Source DB:  PubMed          Journal:  Elife        ISSN: 2050-084X            Impact factor:   8.140


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