The absence of retinal input disrupts the development of cholinergic brainstem projections in the mouse dorsal lateral geniculate nucleus.

Autor: Sokhadze G; Department of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, 511 S. Floyd St, Louisville, KY, 40292, USA., Seabrook TA; Department of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, 511 S. Floyd St, Louisville, KY, 40292, USA., Guido W; Department of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, 511 S. Floyd St, Louisville, KY, 40292, USA. william.guido@louisville.edu.
Jazyk: angličtina
Zdroj: Neural development [Neural Dev] 2018 Dec 12; Vol. 13 (1), pp. 27. Date of Electronic Publication: 2018 Dec 12.
DOI: 10.1186/s13064-018-0124-7
Abstrakt: Background: The dorsal lateral geniculate nucleus (dLGN) of the mouse has become a model system for understanding thalamic circuit assembly. While the development of retinal projections to dLGN has been a topic of extensive inquiry, how and when nonretinal projections innervate this nucleus remains largely unexplored. In this study, we examined the development of a major nonretinal projection to dLGN, the ascending input arising from cholinergic neurons of the brainstem. To visualize these projections, we used a transgenic mouse line that expresses red fluorescent protein exclusively in cholinergic neurons. To assess whether retinal input regulates the timing and pattern of cholinergic innervation of dLGN, we utilized the math5-null (math5 -/- ) mouse, which lacks retinofugal projections due to a failure of retinal ganglion cell differentiation.
Results: Cholinergic brainstem innervation of dLGN began at the end of the first postnatal week, increased steadily with age, and reached an adult-like pattern by the end of the first postnatal month. The absence of retinal input led to a disruption in the trajectory, rate, and pattern of cholinergic innervation of dLGN. Anatomical tracing experiments reveal these disruptions were linked to cholinergic projections from parabigeminal nucleus, which normally traverse and reach dLGN through the optic tract.
Conclusions: The late postnatal arrival of cholinergic projections to dLGN and their regulation by retinal signaling provides additional support for the existence of a conserved developmental plan whereby retinal input regulates the timing and sequencing of nonretinal projections to dLGN.
Databáze: MEDLINE
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