低温制备法定量硬骨鱼角膜原纤维直径

Alan S. Craig , Dav1d A.D. Parry
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引用次数: 5

摘要

采用低温脱水和包埋技术保存了9种硬骨鱼角膜胶原原纤维的横向结构。测量的直径都接近于25.5纳米的值,与“常规”制备的对照物测量的更小(更多样化)的直径形成对比。这一结果与我们早期对哺乳动物、两栖动物、鸟类、爬行动物、软骨和硬骨鱼的角膜的研究结果一致,即硬骨鱼的胶原纤维明显小于其他脊椎动物的胶原纤维。因此,基于低温制备技术保存胶原原纤维结构的增强能力,硬骨鱼的“体内”角膜胶原原纤维直径从17 nm修改为25.5 nm(本研究),所有其他脊椎动物的“体内”角膜胶原原纤维直径从25 nm修改为36 nm(我们之前的研究)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitation of corneal fibril diameters from bony fish using low temperature preparative methods

Low-temperature dehydration and embedding techniques have been used to preserve the transverse structure of corneal collagen fibrils from nine bony fish. The diameters measured all lie close to a value of 25.5 nm, in contrast to the smaller (and more diverse) diameters measured from “conventionally” prepared controls. The results are consistent with our earlier studies on the corneas from mammals, amphibians, birds, reptiles, and cartilaginous and bony fish which showed that the collagen fibrils from the bony fish were significantly smaller than those from animals of the other vertebrate classes. Thus, on the basis of the enhanced ability of the low-temperature preparative techniques to preserve collagen fibril structure the “in vivo” corneal collagen fibril diameters have been revised from 17 to 25.5 nm for bony fish (this work) and from 25 to 36 nm for all other classes of vertebrates (our previous work).

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