BMP Signaling Interferes with Optic Chiasm Formation and Retinal Ganglion Cell Pathfinding in Zebrafish
Decussation of axonal tracts is an important hallmark of vertebrate neuroanatomy resulting in one brain hemisphere controlling the contralateral side of the body and also computing the sensory information originating from that respective side. Here, we show that BMP interferes with optic chiasm form...
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doaj-064ed7e5f0ff4e418c2c88493d1441c22021-04-27T23:02:02ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-04-01224560456010.3390/ijms22094560BMP Signaling Interferes with Optic Chiasm Formation and Retinal Ganglion Cell Pathfinding in ZebrafishMax D. Knickmeyer0Juan L. Mateo1Stephan Heermann2Department of Molecular Embryology, Institute of Anatomy and Cell Biology, Faculty of Medicine, University Freiburg, 79104 Freiburg, GermanyDepartamento de Informática, Universidad de Oviedo, Jesús Arias de Velasco, 33005 Oviedo, SpainDepartment of Molecular Embryology, Institute of Anatomy and Cell Biology, Faculty of Medicine, University Freiburg, 79104 Freiburg, GermanyDecussation of axonal tracts is an important hallmark of vertebrate neuroanatomy resulting in one brain hemisphere controlling the contralateral side of the body and also computing the sensory information originating from that respective side. Here, we show that BMP interferes with optic chiasm formation and RGC pathfinding in zebrafish. Experimental induction of BMP4 at 15 hpf results in a complete ipsilateral projection of RGC axons and failure of commissural connections of the forebrain, in part as the result of an interaction with shh signaling, transcriptional regulation of midline guidance cues and an affected optic stalk morphogenesis. Experimental induction of BMP4 at 24 hpf, resulting in only a mild repression of forebrain shh ligand expression but in a broad expression of pax2a in the diencephalon, does not per se prevent RGC axons from crossing the midline. It nevertheless shows severe pathologies of RGC projections e.g., the fasciculation of RGC axons with the ipsilateral optic tract resulting in the innervation of one tectum by two eyes or the projection of RGC axons in the direction of the contralateral eye.https://www.mdpi.com/1422-0067/22/9/4560chiasmRGC axonsmidlineBMPshhzebrafish |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Max D. Knickmeyer Juan L. Mateo Stephan Heermann |
spellingShingle |
Max D. Knickmeyer Juan L. Mateo Stephan Heermann BMP Signaling Interferes with Optic Chiasm Formation and Retinal Ganglion Cell Pathfinding in Zebrafish International Journal of Molecular Sciences chiasm RGC axons midline BMP shh zebrafish |
author_facet |
Max D. Knickmeyer Juan L. Mateo Stephan Heermann |
author_sort |
Max D. Knickmeyer |
title |
BMP Signaling Interferes with Optic Chiasm Formation and Retinal Ganglion Cell Pathfinding in Zebrafish |
title_short |
BMP Signaling Interferes with Optic Chiasm Formation and Retinal Ganglion Cell Pathfinding in Zebrafish |
title_full |
BMP Signaling Interferes with Optic Chiasm Formation and Retinal Ganglion Cell Pathfinding in Zebrafish |
title_fullStr |
BMP Signaling Interferes with Optic Chiasm Formation and Retinal Ganglion Cell Pathfinding in Zebrafish |
title_full_unstemmed |
BMP Signaling Interferes with Optic Chiasm Formation and Retinal Ganglion Cell Pathfinding in Zebrafish |
title_sort |
bmp signaling interferes with optic chiasm formation and retinal ganglion cell pathfinding in zebrafish |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1661-6596 1422-0067 |
publishDate |
2021-04-01 |
description |
Decussation of axonal tracts is an important hallmark of vertebrate neuroanatomy resulting in one brain hemisphere controlling the contralateral side of the body and also computing the sensory information originating from that respective side. Here, we show that BMP interferes with optic chiasm formation and RGC pathfinding in zebrafish. Experimental induction of BMP4 at 15 hpf results in a complete ipsilateral projection of RGC axons and failure of commissural connections of the forebrain, in part as the result of an interaction with shh signaling, transcriptional regulation of midline guidance cues and an affected optic stalk morphogenesis. Experimental induction of BMP4 at 24 hpf, resulting in only a mild repression of forebrain shh ligand expression but in a broad expression of pax2a in the diencephalon, does not per se prevent RGC axons from crossing the midline. It nevertheless shows severe pathologies of RGC projections e.g., the fasciculation of RGC axons with the ipsilateral optic tract resulting in the innervation of one tectum by two eyes or the projection of RGC axons in the direction of the contralateral eye. |
topic |
chiasm RGC axons midline BMP shh zebrafish |
url |
https://www.mdpi.com/1422-0067/22/9/4560 |
work_keys_str_mv |
AT maxdknickmeyer bmpsignalinginterfereswithopticchiasmformationandretinalganglioncellpathfindinginzebrafish AT juanlmateo bmpsignalinginterfereswithopticchiasmformationandretinalganglioncellpathfindinginzebrafish AT stephanheermann bmpsignalinginterfereswithopticchiasmformationandretinalganglioncellpathfindinginzebrafish |
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1721505386233593856 |