Rózanowski Bartosz, Burke Janice M, Boulton Michael E, Sarna Tadeusz, Rózanowska Małgorzata
Department of Genetics and Cell Biology, Institute of Biology, Pedagogical Academy of Kraków, Kraków, Poland.
Invest Ophthalmol Vis Sci. 2008 Jul;49(7):2838-47. doi: 10.1167/iovs.08-1700. Epub 2008 Mar 7.
To determine the effects of human retinal pigment epithelial (RPE) cell pigment granules on photosensitized and iron ion-mediated oxidation and the effect of the photodegradation of melanosomes on their antioxidant properties.
RPE cells were isolated from human and bovine eyes; pigmented and nonpigmented bovine retinal pigment epithelia were isolated separately. Melanosomes, melanolipofuscin, and lipofuscin granules were isolated from human RPE donors older than 60. Melanosomes were photodegraded by exposure to blue light. Oxidation of RPE cells or of linoleate was induced by iron/ascorbate in the presence and absence of pigment granules. The photosensitized oxidation of histidine was induced by blue light irradiation of cationic porphyrin. The progress of oxidation was monitored by electron spin resonance oximetry.
Iron/ascorbate induced rapid oxidation in suspensions of nonpigmented bovine RPE cells. The rates of oxidation were diminished approximately four times in suspensions of pigmented bovine RPE cells. Adding bovine melanosomes or synthetic melanin to nonpigmented bovine RPE cells resulted in a concentration-dependent decrease in the rate of oxidation to levels similar to those of pigmented bovine retinal pigment epithelium. Human melanosomes exerted a concentration-dependent inhibitory effect on photosensitized and iron-mediated oxidation. Photodegradation of human melanosomes led to loss of the inhibitory effect on iron-mediated oxidation, whereas their ability to inhibit photosensitized oxidation was enhanced.
Human melanosomes act as effective antioxidants by preventing iron ion-induced oxidation. Photodegradation of melanosomes results in the loss of these antioxidant properties while it preserves their ability to deactivate cationic photosensitizers.
确定人视网膜色素上皮(RPE)细胞色素颗粒对光致敏和铁离子介导的氧化作用的影响,以及黑素小体光降解对其抗氧化特性的影响。
从人眼和牛眼中分离RPE细胞;分别分离有色素和无色素的牛视网膜色素上皮。从60岁以上的人RPE供体中分离黑素小体、黑素脂褐素和脂褐素颗粒。通过蓝光照射使黑素小体发生光降解。在有和没有色素颗粒存在的情况下,用铁/抗坏血酸诱导RPE细胞或亚油酸的氧化。通过阳离子卟啉的蓝光照射诱导组氨酸的光致敏氧化。通过电子自旋共振血氧测定法监测氧化进程。
铁/抗坏血酸在无色素牛RPE细胞悬液中诱导快速氧化。在有色素牛RPE细胞悬液中,氧化速率降低了约四倍。向无色素牛RPE细胞中添加牛黑素小体或合成黑色素导致氧化速率呈浓度依赖性降低,降至与有色素牛视网膜色素上皮相似的水平。人黑素小体对光致敏和铁介导的氧化具有浓度依赖性抑制作用。人黑素小体的光降解导致对铁介导氧化的抑制作用丧失,而其抑制光致敏氧化的能力增强。
人黑素小体通过防止铁离子诱导的氧化而起到有效的抗氧化剂作用。黑素小体的光降解导致这些抗氧化特性丧失,同时保留了其使阳离子光致敏剂失活的能力。