Madreperla S A, Edidin M, Adler R
Wilmer Institute, School of Medicine, Baltimore, Maryland.
J Cell Biol. 1989 Oct;109(4 Pt 1):1483-93. doi: 10.1083/jcb.109.4.1483.
We have used isolated embryonic photoreceptor cells as a model system with which to examine the mechanisms responsible for the development and maintenance of asymmetric Na+,K+-ATPase (ATPase) distribution. Photoreceptor precursors, which appear round and process free at culture onset, develop structural and molecular properties similar to those of photoreceptor cells in vivo. ATPase, recognized by an anti-ATPase antibody, is distributed over the entire surface of round photoreceptor precursors. As the cells develop, ATPase becomes progressively concentrated in the inner segment (where it is found in cells of the intact retina). This phenomenon occurs in cells developing in the absence of intercellular contacts. The development of ATPase polarity correlates with a decrease in the fraction of ATPase molecules that are mobile in the membrane (as determined by fluorescence photobleaching recovery), as well as with an increase in the fraction of ATPase that remains associated with the cells after detergent extraction. The magnitudes of the mobile ATPase fractions agree well with those of the detergent-extractable fractions in both the immature and developed photoreceptors. The distribution of alpha spectrin and ATPase-immunoreactive materials appeared qualitatively similar, and quantitative image analysis showed similar gradients of spectrin and Na+,K+-ATPase immunofluorescence along the long axis of elongated photoreceptors. Moreover, detergent extractability of alpha spectrin and the ATPase showed similar modifications in response to changes in pH or KCl concentration. ATPase detergent-extractable and mobile fractions were not changed in cultures treated with cytoskeletal inhibitors such as nocodazole. These data are consistent with a role for an asymmetrically distributed, spectrin-containing subcortical cytoskeleton in the preferential accumulation of Na+,K+-ATPase in the photoreceptor inner segment.
我们使用分离的胚胎光感受器细胞作为模型系统,以研究负责不对称钠钾ATP酶(ATP酶)分布的发育和维持机制。光感受器前体细胞在培养开始时呈圆形且无突起,其发育出的结构和分子特性与体内光感受器细胞相似。抗ATP酶抗体识别的ATP酶分布在圆形光感受器前体细胞的整个表面。随着细胞发育,ATP酶逐渐集中在内段(在完整视网膜的细胞中也能发现)。这种现象发生在没有细胞间接触的发育细胞中。ATP酶极性的发育与膜中可移动的ATP酶分子比例的降低(通过荧光光漂白恢复测定)以及去污剂提取后与细胞保持结合的ATP酶比例的增加相关。在未成熟和发育成熟的光感受器中,可移动ATP酶部分的大小与去污剂可提取部分的大小非常吻合。α-血影蛋白和ATP酶免疫反应性物质的分布在质量上相似,定量图像分析显示,沿着伸长的光感受器的长轴,血影蛋白和钠钾ATP酶免疫荧光具有相似的梯度。此外,α-血影蛋白和ATP酶的去污剂可提取性在响应pH或氯化钾浓度变化时表现出相似的变化。在用细胞骨架抑制剂如诺考达唑处理的培养物中,ATP酶的去污剂可提取部分和可移动部分没有变化。这些数据与不对称分布的、含血影蛋白的皮质下细胞骨架在光感受器内段优先积累钠钾ATP酶中的作用一致。