An opsin 5-dopamine pathway mediates light-dependent vascular development in the eye

. 2019 Apr ; 21 (4) : 420-429. [epub] 20190401

Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid30936473

Grantová podpora
P30 EY006360 NEI NIH HHS - United States
R01 EY022917 NEI NIH HHS - United States
R01 EY032029 NEI NIH HHS - United States
T32 GM063483 NIGMS NIH HHS - United States
P30 EY001730 NEI NIH HHS - United States
R01 EY027711 NEI NIH HHS - United States
R01 EY014648 NEI NIH HHS - United States
R01 EY004864 NEI NIH HHS - United States
R01 EY026921 NEI NIH HHS - United States
R01 EY027077 NEI NIH HHS - United States
R01 GM124246 NIGMS NIH HHS - United States

Odkazy

PubMed 30936473
PubMed Central PMC6573021
DOI 10.1038/s41556-019-0301-x
PII: 10.1038/s41556-019-0301-x
Knihovny.cz E-zdroje

During mouse postnatal eye development, the embryonic hyaloid vascular network regresses from the vitreous as an adaption for high-acuity vision. This process occurs with precisely controlled timing. Here, we show that opsin 5 (OPN5; also known as neuropsin)-dependent retinal light responses regulate vascular development in the postnatal eye. In Opn5-null mice, hyaloid vessels regress precociously. We demonstrate that 380-nm light stimulation via OPN5 and VGAT (the vesicular GABA/glycine transporter) in retinal ganglion cells enhances the activity of inner retinal DAT (also known as SLC6A3; a dopamine reuptake transporter) and thus suppresses vitreal dopamine. In turn, dopamine acts directly on hyaloid vascular endothelial cells to suppress the activity of vascular endothelial growth factor receptor 2 (VEGFR2) and promote hyaloid vessel regression. With OPN5 loss of function, the vitreous dopamine level is elevated and results in premature hyaloid regression. These investigations identify violet light as a developmental timing cue that, via an OPN5-dopamine pathway, regulates optic axis clearance in preparation for visual function.

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