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Neuropsin (OPN5)-mediated photoentrainment of local circadian oscillators in mammalian retina and cornea. | LitMetric

AI Article Synopsis

  • Molecular circadian clocks in the mammalian retina can sync with environmental light cycles without relying on the brain's suprachiasmatic nuclei (SCN) or traditional photoreceptors like rods and cones.
  • The study found that short-wavelength light is crucial for this process, but does not depend on the previously known photopigments like S-pigment or encephalopsin.
  • Neuropsin (OPN5) is essential for photoentrainment in the retina and cornea, highlighting its previously underappreciated role as a light-sensing opsin.

Article Abstract

The molecular circadian clocks in the mammalian retina are locally synchronized by environmental light cycles independent of the suprachiasmatic nuclei (SCN) in the brain. Unexpectedly, this entrainment does not require rods, cones, or melanopsin (OPN4), possibly suggesting the involvement of another retinal photopigment. Here, we show that the ex vivo mouse retinal rhythm is most sensitive to short-wavelength light but that this photoentrainment requires neither the short-wavelength-sensitive cone pigment [S-pigment or cone opsin (OPN1SW)] nor encephalopsin (OPN3). However, retinas lacking neuropsin (OPN5) fail to photoentrain, even though other visual functions appear largely normal. Initial evidence suggests that OPN5 is expressed in select retinal ganglion cells. Remarkably, the mouse corneal circadian rhythm is also photoentrainable ex vivo, and this photoentrainment likewise requires OPN5. Our findings reveal a light-sensing function for mammalian OPN5, until now an orphan opsin.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620855PMC
http://dx.doi.org/10.1073/pnas.1516259112DOI Listing

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