Owusu-Ansah Kofi, Pham Dylan L, Strong Brower C, Liberoni Lora, Hein Travis W, Kuo Lih, Ko Michael Lee, Ko Gladys Yi-Ping
Department of Veterinary Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas, United States.
Texas A&M Institute for Neuroscience, Texas A&M University, College Station, Texas, United States.
Invest Ophthalmol Vis Sci. 2025 May 1;66(5):37. doi: 10.1167/iovs.66.5.37.
Peptide Lv (PLv) is a small endogenous secretory peptide expressed in various organs, including the retina and brain. It augments the protein expression and current densities of the L-type voltage-gated calcium channels in photoreceptors, hence the name peptide "Lv." However, its physiological function in the neural retina remains unknown. This study aims to determine the role of PLv in the retina using PLv null (PLv-/-) mice.
Both male and female PLv-/- and age-matched control (PLv+/+) littermates were assessed longitudinally. The retinal light responses were examined using dark-adapted electroretinography (ERG). The thicknesses for whole retinas and various retinal layers were evaluated through spectral-domain optical coherence tomography (SD-OCT) and hematoxylin and eosin staining of retinal sections.
Dark-adapted ERG a-wave, b-wave, and oscillatory potentials were compromised in PLv-/- mice, which were more severe in females at younger ages. The whole retina and outer nuclear layer in PLv-/- mice were progressively thinner than the controls, as observed in SD-OCT imaging, which was corroborated by the histologic analyses of retinal sections. The progression of age-related retinal thinning was significantly slower in females than in males in both PLv-/- and PLv+/+ mice.
Peptide Lv contributes to the maintenance of the structural and functional integrity of adult retinas, and its deficiency accelerates retinal degeneration. These findings highlight a potential neuroprotective role of peptide Lv in the retina.
肽Lv(PLv)是一种在包括视网膜和大脑在内的多种器官中表达的内源性小分泌肽。它增强了光感受器中L型电压门控钙通道的蛋白表达和电流密度,因此得名肽“Lv”。然而,其在神经视网膜中的生理功能尚不清楚。本研究旨在利用PLv基因敲除(PLv-/-)小鼠确定PLv在视网膜中的作用。
对雄性和雌性PLv-/-小鼠以及年龄匹配的对照(PLv+/+)同窝小鼠进行纵向评估。使用暗适应视网膜电图(ERG)检测视网膜光反应。通过光谱域光学相干断层扫描(SD-OCT)和视网膜切片的苏木精和伊红染色评估整个视网膜和各个视网膜层的厚度。
PLv-/-小鼠的暗适应ERG a波、b波和振荡电位受损,在年龄较小的雌性小鼠中更为严重。如SD-OCT成像所示,PLv-/-小鼠的整个视网膜和外核层逐渐比对照组薄,视网膜切片的组织学分析证实了这一点。在PLv-/-和PLv+/+小鼠中,雌性与年龄相关的视网膜变薄进展明显比雄性慢。
肽Lv有助于维持成年视网膜的结构和功能完整性,其缺乏会加速视网膜变性。这些发现突出了肽Lv在视网膜中的潜在神经保护作用。