232 research outputs found

    Visual Pigments and Light Detection in the Eye

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    Most forms of animal vision begin with light absorption by visual pigments in the eye. A typical visual pigment consists of a G protein-coupled receptor protein – opsin – covalently conjugated to a chromophore. Sub-families of opsins show distinctive physicochemical properties and cellular expressions, often attuned to the specific visual functions that they serve. Here, we examined a number of molecular and functional features of three sub-families of opsins. We found that: (1) an active molecule of rhodopsin (a ciliary opsin expressed in rod photoreceptors for dim-light vision) amplifies the light signal by activating about 20-30 transducin molecules at the peak of the current response to single photon-absorption. (2) the thermal activation of native and some mutant rhodopsin and cone pigments (ciliary opsins in cone photoreceptors for color vision) in the dark is indeed an isomerization event, the rate of which can be quantitatively predicted by multi-vibrational-mode statistical mechanics. (3) melanopsin, a rhabdomeric opsin that underlies the intrinsic photosensitivity of a subgroup of retinal ganglion cells and is responsible for diverse non-image-forming visual functions in mammals, is also expressed in some thick, myelinated neuronal processes in the rat iris that possibly originate from the trigeminal ganglia. (4) neuropsin (OPN5), a previous orphan opsin, mediates the photoentrainment of the local circadian rhythm in the mammalian retina and cornea

    Implantation of neural stem cells embedded in hyaluronic acid and collagen composite conduit promotes regeneration in a rabbit facial nerve injury model

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    The implantation of neural stem cells (NSCs) in artificial scaffolds for peripheral nerve injuries draws much attention. NSCs were ex-vivo expanded in hyaluronic acid (HA)-collagen composite with neurotrophin-3, and BrdU-labeled NSCs conduit was implanted onto the ends of the transected facial nerve of rabbits. Electromyography demonstrated a progressive decrease of current threshold and increase of voltage amplitude in de-innervated rabbits after implantation for one, four, eight and 12 weeks compared to readouts derived from animals prior to nerve transection. The most remarkable improvement, observed using Electrophysiology, was of de-innervated rabbits implanted with NSCs conduit as opposed to de-innervated counterparts with and without the implantation of HA-collagen, NSCs and HA-collagen, and HA-collagen and neurotrophin-3. Histological examination displayed no nerve fiber in tissue sections of de-innervated rabbits. The arrangement and S-100 immunoreactivity of nerve fibers in the tissue sections of normal rabbits and injured rabbits after implantation of NSCs scaffold for 12 weeks were similar, whereas disorderly arranged minifascicles of various sizes were noted in the other three arms. BrdU+ cells were detected at 12 weeks post-implantation. Data suggested that NSCs embedded in HA-collagen biomaterial could facilitate re-innervations of damaged facial nerve and the artificial conduit of NSCs might offer a potential treatment modality to peripheral nerve injuries

    Ground movements due to deep excavations in Shanghai:Design charts

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