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Bhoi, J. D.

Publications and source records attributed to Bhoi, J. D..

3 recordsLinked to original sources

SEX-DEPENDENT MODULATION OF WHOLE BRAIN cFOS EXPRESSION BY LIGHT AND MELANOPSIN IN THE MOUSE

Light is a fundamental feature of the environment, signaling time of day, weather changes, approaching predators, and other survival cues. The extensive projections from the retina to the brain provide an anatomical substrate for light to adaptively tune circuit function based on changing environmental light. Yet we understand little about the scope and functional impact of light outside of visual and circadian circuits. To address this, we created a whole-brain atlas of light-induced cFos expression in the mouse brain. This approach yielded a strikingly broad pattern of light-driven cFos activation throughout the brain that extended beyond canonical visual circuits, with unexpectedly strong modulation of neuromodulatory centers. These patterns differed starkly in males and females, and were dependent primarily on melanopsin-expressing, intrinsically photosensitive retinal ganglion cells. These findings uncover surprising brainwide patterns of light modulation and are shared as an interactive resource so that they can inspire new, future studies.

neuroscience↗

Melanopsin contributes to circadian photic responses in mice in a sex-dependent manner

Proper entrainment of the bodys circadian rhythms to the environment is critical to human health. Light is one of the strongest cues driving circadian photoentrainment of the central circadian pacemaker, the suprachiasmatic nucleus (SCN), via projections from the melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs). Circadian research has historically centered males, and recent work has revealed multiple sex-differences in circadian circuitry and function, indicating that our understanding of this system in females is severely limited. Moreover, while recent studies have investigated the role of hormonal modulation of light responses, the additional possibility that ipRGC inputs may also be sex-dependent has not been directly tested. Here, we report that not only do ipRGCs in female mice show higher levels of melanopsin expression, but that melanopsin also plays a larger role in shaping circadian photic responses in females compared to males. Collectively, these results define a new retinal source for sex-dependent differences in circadian behavior.

neuroscience↗

Genetic tuning of intrinsically photosensitive retinal ganglion cell subtype identity to drive visual behavior

The melanopsin-expressing, intrinsically photosensitive retinal ganglion cells (ipRGCs) comprise a subset of the [~]40 retinal ganglion cell types in the mouse retina and drive a diverse array of light-evoked behaviors from circadian photoentrainment to pupil constriction to contrast sensitivity for visual perception. Central to the ability of ipRGCs to control this diverse array of behaviors is the distinct complement of morphophysiological features and gene expression patterns found in the M1-M6 ipRGC subtypes. However, the genetic regulatory programs that give rise to subtypes of ipRGCs are unknown. Here, we identify the transcription factor Brn3b (Pou4f2) as a key genetic regulator that shapes the unique functions of ipRGC subtypes and their diverse downstream visual behaviors.

neuroscience↗