Hossler F E
Am J Physiol. 1980 Mar;238(3):R160-4. doi: 10.1152/ajpregu.1980.238.3.R160.
The rate of response of gill filament epithelium to salinity changes was determined by scanning electron microscopy and biochemical techniques. An increase in Na-K-ATPase content, as measured by [3H]ouabain binding, was detected at 3 h and continued to about 24 h after mullet were transferred from a salinity of 1-4.5%. In contrast, filaments from mullet transferred to freshwater exhibited a decrease in ouabain-binding sites. Similarly, scanning electron microscopy revealed that ultrastructural modifications occurred in epithelial pores of the filament surface in response to salinity changes. These modifications, which included changes in pore diameter and depth and in the number of cellular extensions in the pore's interior, were evident as early as 6 h and were mostly completed by 24 h after the salinity change. Because epithelial pores likely represent apical pits of chloride cells and because the Na-K-ATPase is localized within chloride cells, the present observations likely represent different manifestations of the very rapid response of chloride cells to osmotic stress, and indicate the close association of structure with function.
通过扫描电子显微镜和生化技术测定了鳃丝上皮对盐度变化的反应速率。用[3H]哇巴因结合法测定,鲻鱼从盐度1-4.5%转移后3小时,钠钾ATP酶含量增加,并持续至约24小时。相反,转移到淡水中的鲻鱼的鳃丝显示哇巴因结合位点减少。同样,扫描电子显微镜显示,鳃丝表面上皮孔的超微结构因盐度变化而发生改变。这些改变包括孔径和深度以及孔内细胞延伸数量的变化,早在盐度变化后6小时就很明显,大多在24小时内完成。由于上皮孔可能代表氯细胞的顶端小窝,且钠钾ATP酶定位于氯细胞内,目前的观察结果可能代表氯细胞对渗透应激的非常快速反应的不同表现,并表明结构与功能密切相关。