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Housset, M.

Publications and source records attributed to Housset, M..

2 recordsLinked to original sources

A Müller glia-retinal pigment epithelium apical network surrounding cone outer segments in fish and mouse

Homeostasis of the vertebrate retina is supported by two non-neuronal cell types, Muller glia and the retinal pigment epithelium (RPE). Their apical domains delineate the subretinal space, where photoreceptor outer segments reside. While the individual interactions between the supporting cells and photoreceptors are well studied, Muller glia and RPE are presumed to remain physically separate in a healthy retina. Here, we describe a revised model of the subretinal space architecture based on detailed FIB-SEM and confocal microscopy imaging of the zebrafish and mouse outer retina. Long apical processes extend from both Muller glia and the RPE, interacting with one another while also encircling cone outer segments. These contact regions, at the interface of the three cell types are highly elaborated in fish and, although sparser, are still present in mouse. The growth and overlap of Muller glial and RPE apical processes occurs subsequent to the emergence of the outer segment in both species, and coincides with the onset of visual function in mouse. Although enriched at cone sites, this specialized interaction does not appear to depend solely on cone localization in either species, pointing to a general hallmark of the vertebrate subretinal space. Together, our work provides major insights into the architecture of the subretinal space and the interactions between Muller glia, RPE and photoreceptors, while demonstrating conservation across species.

cell biology↗

Light-mediated planar polarization of cone photoreceptorcilia contributes to visual acuity in mammals

The coordinated spatial arrangement of organelles within a tissue plane, generally referred to as Planar Cell Polarity (PCP), is critical for various processes ranging from organogenesis to sensory detection. Mechanistically, planar cell polarity is typically set-up by gradients of morphogens and their receptors, but whether non-molecular cues, akin to phototropism in plants, might play a part in setting up PCP in animals remains unknown. Here we report that the basal body of newborn photoreceptor cells in the mouse retina is centrally positioned, but then moves laterally around the first post-natal week, thereby generating cell-intrinsic asymmetry. During the second postnatal week, when eyes open, the basal bodies of cone photoreceptor cilia, but not rods, become coordinated across the tissue plane to face the center of the retina. Mechanistically, we show that light is required during a critical window in development, triggering a non-canonical cascade whereby cone transducin interacts with the G- protein signaling modulator protein 2 (GPSM2), which is in turn necessary for cone PCP. This work uncovers a non-canonical PCP pathway initiated by light.

cell biology↗