Yang W C, Hollenberg M J, Wyse J P
Virchows Arch B Cell Pathol. 1978 Mar 2;27(1):7-21. doi: 10.1007/BF02888979.
Ultrastructural changes in the retinal pigment epithelium (RPE) and adjacent photoreceptor cells have been followed in the Wistar rat during the course of long-term vitamin A deficiency. Of particular interest has been the discovery of unusual concentric aggregates within the photoreceptor outer segments and the inner cytoplasm of the RPE. The aggregates were present throughout the course of the retinal degeneration induced by vitamin A deficiency and could be identified in the RPE either by themselves in the apical cytoplasm or within phagolysosomes. It is postulated that the concentric aggregates result initially from abnormal formation or condensation of outer segment membranes and are then slowly degraded by lysosomal action in the RPE cytoplasm. In addition, acid phosphatase activity and typical phagosomes (shed outer segment packets) have been demonstrated in the cytoplasm of the RPE of the vitamin A deficient rats. The latter findings indicate that, at least to some extent, the normal phagocytic and lytic processes of the RPE are retained in this nutritional disorder.
在长期维生素A缺乏的过程中,对Wistar大鼠视网膜色素上皮(RPE)和相邻光感受器细胞的超微结构变化进行了跟踪研究。特别令人感兴趣的是,在光感受器外段和RPE的内细胞质中发现了异常的同心聚集体。这些聚集体在维生素A缺乏引起的视网膜变性过程中一直存在,并且可以在RPE的顶端细胞质中单独识别,也可以在吞噬溶酶体中识别。据推测,同心聚集体最初是由外段膜的异常形成或凝聚产生的,然后在RPE细胞质中被溶酶体作用缓慢降解。此外,在维生素A缺乏大鼠的RPE细胞质中已证实存在酸性磷酸酶活性和典型的吞噬体(脱落的外段包)。后一发现表明,在这种营养紊乱中,RPE的正常吞噬和溶解过程至少在一定程度上得以保留。