铁超载和螯合调节视网膜中的双维甲酸水平

Jin Zhao, H. J. Kim, Diego Montenegro, Josh L. Dunaief, Janet R. Sparrow
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引用次数: 0

摘要

铁失调与其他疾病过程结合可能会加剧视网膜变性。我们利用铁过载和铁螯合模型来探索铁催化的氧化作用与光活性双视色素脂褐质之间的相互作用。小鼠从出生到2个月大期间,经玻璃体内注射枸橼酸铁铵(FAC)或使用铁螯合剂去铁酮(DFP)进行治疗。研究人员采集了短波长眼底自动荧光(SW-AF)和光谱域光学相干断层扫描(SD-OCT)扫描图像。使用超高效液相色谱法(UPLC)对双维甲酸水平进行量化,并通过定量眼底自动荧光(qAF)对体内双维甲酸水平进行量化。在组织学切片中,通过测量核外层(ONL)的厚度来评估感光细胞的存活率。在注射了 FAC 的 C57BL/6J 小鼠眼中,双视色素、全反式视网膜二聚体和 A2PE 的含量显著增加。注射 FAC 七天后,在眼底自动荧光(488 nm)图像中可见高自荧光灶,在 SD-OCT 扫描中,外层视网膜出现异常高反射,并观察到 ONL 变薄。在注射了 FAC 的 Abca4-/- 小鼠中,RPE 双脂质脂褐素蓄积明显,高自荧光点比野生型小鼠更多,ONL 变薄的程度也更大。相反,在 Mertk-/- 小鼠体内注射 FAC 2 天后,A2PE 的增加幅度较小。与铁蓄积的影响相反,用 DFP 螯合会导致 A2E、A2-GPE 和 qAF 水平显著增加,原因是减少了铁催化的双维甲酸氧化。与 DFP 处理的小鼠相比,Mertk-/- 小鼠的 A2E 水平明显降低,ONL 面积变小。铁的积累与光感受器细胞的渐进性损伤有关,而这种损伤与光感受器外节中作为 A2E 前体的一种已知的双类视黄醇的形成增加有关。此外,当向双视色素形成倾向更强的 Abca4-/- 小鼠输送铁时,疾病特征(如眼底 AF 图像中出现高荧光点、SD-OCT 扫描的外层视网膜出现高反射和 ONL 变薄)更加明显。较高的双视黄醇水平和增强的qAF表明氧化导致的双视黄醇损失较少。
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Iron overload and chelation modulates bisretinoid levels in the retina
Iron dysregulation in conjunction with other disease processes may exacerbate retinal degeneration. We employed models of iron overload and iron chelation to explore the interactions between iron-catalyzed oxidation and photoreactive bisretinoid lipofuscin.The mice were injected intravitreally with ferric ammonium citrate (FAC) or were treated using the iron chelator deferiprone (DFP) from birth to 2 months of age. Short-wavelength fundus autofluorescence (SW-AF) and spectral-domain optical coherence tomography (SD-OCT) scans were acquired. The bisretinoid levels were quantified using ultra performance liquid chromatography (UPLC) and in vivo through quantitative fundus autofluorescence (qAF). In histologic sections, the photoreceptor cell viability was assessed by measuring the thickness of the outer nuclear layer (ONL).The levels of bisretinoids, all-trans-retinal dimers, and A2PE were significantly increased in the FAC-injected eyes of C57BL/6J mice. Seven days after FAC injection, hyperautofluorescent foci were visible in fundus autofluorescence (488 nm) images, and in SD-OCT scans, aberrant hyperreflectivity was present in the outer retina and ONL thinning was observed. In FAC-injected Abca4–/– mice with pronounced RPE bisretinoid lipofuscin accumulation, the hyperautofluorescent puncta were more abundant than in the wild-type mice, and the extent of ONL thinning was greater. Conversely, the intravitreal injection of FAC in Mertk–/– mice led to a more modest increase in A2PE after 2 days. In contrast to the effect of iron accumulation, chelation with DFP resulted in significantly increased levels of A2E and A2-GPE and qAF due to the reduced iron-catalyzed oxidation of bisretinoids. In Mertk–/– mice, the A2E level was significantly lower and the ONL area was smaller than in DFP-treated mice. DFP chelation did not impair the visual cycle in BALB/cJ mice.Iron accumulation was associated with progressive impairment in photoreceptor cells that was associated with the increased formation of a bisretinoid species known to form in photoreceptor outer segments as a precursor to A2E. Additionally, disease features such as the development of hyperautofluorescence puncta in fundus AF images, hyperreflectivity in the outer retina of SD-OCT scans, and ONL thinning were more pronounced when iron was delivered to Abca4–/– mice with a greater propensity for bisretinoid formation. Higher bisretinoid levels and enhanced qAF are indicative of lesser bisretinoid loss due to oxidation.
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