Cargando…

Eph/ephrin Function Contributes to the Patterning of Spinocerebellar Mossy Fibers Into Parasagittal Zones

Purkinje cell microcircuits perform diverse functions using widespread inputs from the brain and spinal cord. The formation of these functional circuits depends on developmental programs and molecular pathways that organize mossy fiber afferents from different sources into a complex and precisely pa...

Descripción completa

Detalles Bibliográficos
Autores principales: Lackey, Elizabeth P., Sillitoe, Roy V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033604/
https://www.ncbi.nlm.nih.gov/pubmed/32116578
http://dx.doi.org/10.3389/fnsys.2020.00007
_version_ 1783499706156974080
author Lackey, Elizabeth P.
Sillitoe, Roy V.
author_facet Lackey, Elizabeth P.
Sillitoe, Roy V.
author_sort Lackey, Elizabeth P.
collection PubMed
description Purkinje cell microcircuits perform diverse functions using widespread inputs from the brain and spinal cord. The formation of these functional circuits depends on developmental programs and molecular pathways that organize mossy fiber afferents from different sources into a complex and precisely patterned map within the granular layer of the cerebellum. During development, Purkinje cell zonal patterns are thought to guide mossy fiber terminals into zones. However, the molecular mechanisms that mediate this process remain unclear. Here, we used knockout mice to test whether Eph/ephrin signaling controls Purkinje cell-mossy fiber interactions during cerebellar circuit formation. Loss of ephrin-A2 and ephrin-A5 disrupted the patterning of spinocerebellar terminals into discrete zones. Zone territories in the granular layer that normally have limited spinocerebellar input contained ectopic terminals in ephrin-A2(−/−);ephrin-A5(−/−) double knockout mice. However, the overall morphology of the cerebellum, lobule position, and Purkinje cell zonal patterns developed normally in the ephrin-A2(−/−);ephrin-A5(−/−) mutant mice. This work suggests that communication between Purkinje cell zones and mossy fibers during postnatal development allows contact-dependent molecular cues to sharpen the innervation of sensory afferents into functional zones.
format Online
Article
Text
id pubmed-7033604
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-70336042020-02-28 Eph/ephrin Function Contributes to the Patterning of Spinocerebellar Mossy Fibers Into Parasagittal Zones Lackey, Elizabeth P. Sillitoe, Roy V. Front Syst Neurosci Neuroscience Purkinje cell microcircuits perform diverse functions using widespread inputs from the brain and spinal cord. The formation of these functional circuits depends on developmental programs and molecular pathways that organize mossy fiber afferents from different sources into a complex and precisely patterned map within the granular layer of the cerebellum. During development, Purkinje cell zonal patterns are thought to guide mossy fiber terminals into zones. However, the molecular mechanisms that mediate this process remain unclear. Here, we used knockout mice to test whether Eph/ephrin signaling controls Purkinje cell-mossy fiber interactions during cerebellar circuit formation. Loss of ephrin-A2 and ephrin-A5 disrupted the patterning of spinocerebellar terminals into discrete zones. Zone territories in the granular layer that normally have limited spinocerebellar input contained ectopic terminals in ephrin-A2(−/−);ephrin-A5(−/−) double knockout mice. However, the overall morphology of the cerebellum, lobule position, and Purkinje cell zonal patterns developed normally in the ephrin-A2(−/−);ephrin-A5(−/−) mutant mice. This work suggests that communication between Purkinje cell zones and mossy fibers during postnatal development allows contact-dependent molecular cues to sharpen the innervation of sensory afferents into functional zones. Frontiers Media S.A. 2020-02-13 /pmc/articles/PMC7033604/ /pubmed/32116578 http://dx.doi.org/10.3389/fnsys.2020.00007 Text en Copyright © 2020 Lackey and Sillitoe. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Lackey, Elizabeth P.
Sillitoe, Roy V.
Eph/ephrin Function Contributes to the Patterning of Spinocerebellar Mossy Fibers Into Parasagittal Zones
title Eph/ephrin Function Contributes to the Patterning of Spinocerebellar Mossy Fibers Into Parasagittal Zones
title_full Eph/ephrin Function Contributes to the Patterning of Spinocerebellar Mossy Fibers Into Parasagittal Zones
title_fullStr Eph/ephrin Function Contributes to the Patterning of Spinocerebellar Mossy Fibers Into Parasagittal Zones
title_full_unstemmed Eph/ephrin Function Contributes to the Patterning of Spinocerebellar Mossy Fibers Into Parasagittal Zones
title_short Eph/ephrin Function Contributes to the Patterning of Spinocerebellar Mossy Fibers Into Parasagittal Zones
title_sort eph/ephrin function contributes to the patterning of spinocerebellar mossy fibers into parasagittal zones
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033604/
https://www.ncbi.nlm.nih.gov/pubmed/32116578
http://dx.doi.org/10.3389/fnsys.2020.00007
work_keys_str_mv AT lackeyelizabethp ephephrinfunctioncontributestothepatterningofspinocerebellarmossyfibersintoparasagittalzones
AT sillitoeroyv ephephrinfunctioncontributestothepatterningofspinocerebellarmossyfibersintoparasagittalzones