SIDMAN R L
J Biophys Biochem Cytol. 1957 Jan 25;3(1):15-30. doi: 10.1083/jcb.3.1.15.
Fragments of freshly obtained retinas of several vertebrate species were studied by refractometry, with reference to the structure of the rods and cones. The findings allowed a reassessment of previous descriptions based mainly on fixed material. The refractometric method was used also to measure the refractice indices and to calculate the concentrations of solids and water in the various cell segments. The main quantitative data were confirmed by interference microscopy. When examined by the method of refractometry the outer segments of freshly prepared retinal rods appear homogeneous. Within a few minutes a single eccentric longitudinal fiber appears, and transverse striations may develop. These changes are attributed to imbibition of water and swelling in structures normally too small for detection by light microscopy. The central "core" of outer segments and the chromophobic disc between outer and inner segments appear to be artifacts resulting from shrinkage during dehydration. The fresh outer segments of cones, and the inner segments of rods and cones also are described and illustrated. The volumes, refractive indices, concentrations of solids, and wet and dry weights of various segments of the photoreceptor cells were tabulated. Rod outer segments of the different species vary more than 100-fold in volume and mass but all have concentrations of solids of 40 to 43 per cent. Cone outer segments contain only about 30 per cent solids. The myoids, paraboloids, and ellipsoids of the inner segments likewise have characteristic refractive indices and concentrations of solids. Some of the limitations and particular virtues of refractometry as a method for quantitative analysis of living cells are discussed in comparison with more conventional biochemical techniques. Also the shapes and refractive indices of the various segments of photoreceptor cells are considered in relation to the absorption and transmission of light. The Stiles-Crawford effect can be accounted for on the basis of the structure of cone cells.
通过折射测量法研究了几种脊椎动物新鲜获取的视网膜碎片,并参考了视杆细胞和视锥细胞的结构。这些发现使得能够重新评估之前主要基于固定材料的描述。折射测量法还用于测量折射率,并计算各个细胞段中固体和水的浓度。主要定量数据通过干涉显微镜得到了证实。用折射测量法检查时,新鲜制备的视网膜视杆细胞的外段看起来是均匀的。几分钟内会出现一条偏心纵向纤维,并且可能会形成横向条纹。这些变化归因于水的吸收以及结构膨胀,这些结构通常太小而无法通过光学显微镜检测到。外段的中央“核心”以及外段和内段之间的嗜色盘似乎是脱水过程中收缩产生的假象。还描述并说明了视锥细胞的新鲜外段以及视杆细胞和视锥细胞的内段。列出了光感受器细胞各个段的体积、折射率、固体浓度以及湿重和干重。不同物种的视杆细胞外段在体积和质量上变化超过100倍,但所有外段的固体浓度均为40%至43%。视锥细胞外段仅含有约30%的固体。内段的肌样体、抛物面和椭球体同样具有特征性的折射率和固体浓度。与更传统的生化技术相比,讨论了折射测量法作为活细胞定量分析方法的一些局限性和特殊优点。还根据光的吸收和透射考虑了光感受器细胞各个段的形状和折射率。基于视锥细胞的结构可以解释斯泰尔斯 - 克劳福德效应。