Photoreceptors, as polarized sensory neurons, are essential for light sensation and phototransduction, which are highly dependent on the photoreceptor cilium. Disruption of photoreceptor cilia has been implicated in a variety of retinal diseases, collectively called retinociliopathies, such as Leber congenital amaurosis and retinopathy of prematurity.
Recently, teams led by Prof. Jun Zhou and Assoc Prof. Jie Ran from Shandong Normal University revealed that ciliary disassembly in photoreceptors is a significant event in the pathogenesis of RD.
Their work demonstrated a significant reduction in retinal electrophysiological a-wave and b-wave responses and a marked decrease in the thickness of the outer nuclear layer (ONL) in RD mice, indicating severe damage to photoreceptors. Transmission electron microscopy and immunofluorescence microscopy analyses revealed varying degrees of damage to photoreceptor membrane discs and ciliary axonemes. These results indicate that photoreceptor ciliary disassembly is a key event triggering photoreceptor dysfunction and retinal damage in the pathological process of RD (Figure 1).
In general, their study elucidates the significant role of photoreceptor cilia in RD and provides novel targets for clinical intervention in RD. Graduate students Guizhi Guo and Runa Wang from Shandong Normal University are the first authors of this work, with Assoc Prof. Jie Ran as the corresponding author. This research was supported by grants from the National Natural Science Foundation of China (32170687, 32241014).
