Kaplan M W
R. S. Dow Neurological Sciences Institute, Portland, OR 97209-1595, USA.
Curr Eye Res. 1998 Jan;17(1):73-8. doi: 10.1076/ceyr.17.1.73.5248.
Mechanisms that maintain the close coupling between the formation of photoreceptor disk membranes and the displacement of disk membranes toward the pigment epithelium are poorly understood. This study was designed to determine whether the axial displacement of disk membranes requires the assembly and insertion of new disk lamellae.
Retinal detachment and treatment with cytochalasin D were employed to interrupt the normal formation of disk membranes in cultured Xenopus laevis retinas. The effect of disrupting disk initiation and assembly upon disk displacement was documented and quantified.
Isolating retinas from the retinal pigment epithelium prevented the normal morphogenesis of disks, but previously formed disks moved distally at a rate that is greater than or equal to the rate in attached retinas or in vivo. Treatment of attached retinas in eyecups with cytochalasin D blocked initiation of new disks and resulted in the formation of ectopic, disk-like membranes, but it did not stop axial displacement of previously formed disks. Rod cells in retinas that were cultured while slightly elevated from the retinal pigment epithelium sometimes formed disks of a smaller diameter than normal, even though the rate of initiation and displacement of disks was the same as in vivo.
Observations on detached retinas and or retinas treated with cytochalasin D suggest that disk displacement does not depend upon normal disk formation and that the motive mechanism does not involve filamentous actin. The formation of small diameter disks in elevated retinas suggests that disk initiation and displacement is independent of the completion of normal diameter disks.
维持光感受器盘膜形成与盘膜向色素上皮移位之间紧密偶联的机制尚不清楚。本研究旨在确定盘膜的轴向移位是否需要新盘片层的组装和插入。
采用视网膜脱离和细胞松弛素D处理,以中断培养的非洲爪蟾视网膜中盘膜的正常形成。记录并量化破坏盘起始和组装对盘移位的影响。
将视网膜与视网膜色素上皮分离会阻止盘的正常形态发生,但先前形成的盘以大于或等于附着视网膜或体内的速率向远端移动。用细胞松弛素D处理眼杯中的附着视网膜会阻止新盘的起始,并导致异位盘状膜的形成,但它不会阻止先前形成的盘的轴向移位。在从视网膜色素上皮略微抬高的情况下培养的视网膜中的视杆细胞有时会形成直径小于正常的盘,尽管盘的起始和移位速率与体内相同。
对脱离视网膜和/或用细胞松弛素D处理的视网膜的观察表明,盘移位不依赖于正常的盘形成,并且驱动机制不涉及丝状肌动蛋白。抬高的视网膜中形成小直径盘表明盘的起始和移位与正常直径盘的完成无关。