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A systematic assessment of goblet cell sampling of the bulbar conjunctiva by impression cytology

机译:通过印模细胞学进行泡杆结膜的脚卵细胞采样的系统评估

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The purpose of this study was to assess the apparent goblet cell density (GCD) from conjunctival impression cytology (CIC) samples in relation to the number of conjunctival cells collected onto the filters. CIC specimens were collected from the superior-temporal bulbar conjunctiva of 16 pigmented rabbits onto Biopore (Millicell-CM) membranes, fixed with buffered glutaraldehyde and stained with Giemsa. Different numbers of microscope fields of view in each of the specimens were imaged by light microscopy using a 20x magnification objective lens (200x final magnification), and the goblet cells marked and counted. The GCD values/sq. mm were calculated. The same conjunctival region of 3 other rabbits was also prepared for transmission electron microscopy (TEM) by fixation, in situ, with the same buffered glutaraldehyde. Mean values for GCD estimates were found to vary from 399 to 1576 cells/sq. mm, depending on the image sampling and analysis strategy chosen, with the lowest inter-sample variance of around 10% being found if a maximum goblet cell count was taken on substantially multilayered regions of the CIC specimens. Counts of the number of goblet cells per 1000 visible conjunctival epithelial cells yielded a value of close to 90 (range 36-151), with modest inter-sample variability of around 30%. A three or ten 200x microscope field and random sampling strategy yielded mean GCD values between 542 and 670 cells/sq. mm, but with very high intra-and inter-sample variance of at least 60% and sometimes higher than 100%. TEM confirmed the multilayered organization of the conjunctiva and the deeper lying goblet cells. The general use of a goblet cell count as an objective marker for conjunctival normality or health is likely to be highly variable unless a more specific strategy is adopted. Beyond providing details of exactly the counting strategy used, it would be very useful to provide full details of the actual microscope field size used as well as information on the intra-sample variability in goblet cell counts. (C) 2015 Elsevier Ltd. All rights reserved.
机译:本研究的目的是评估来自结膜印象细胞学(CIC)样品的表观脚卵细胞密度(GCD)与收集在过滤器上的结膜细胞的数量。将CIC标本从16种着色的兔的上颞块结膜收集到生物植物(毫钙-CM)膜上,用缓冲的戊二醛固定并用Giemsa染色。使用20倍放大镜物镜(200倍最终放大倍数),通过光学显微镜对每个标本中的每个样本中的不同数量的显微镜视图进行成像,并且标记和计数的脚螺旋细胞。 GCD值/ SQ。计算mm。通过用相同的缓冲谷氨酸的固定,还为透射电子显微镜(TEM)制备相同的3个其他兔子的结膜区域。发现GCD估计的平均值从399到1576个细胞/平方米不同。根据所选择的图像采样和分析策略,如果在CIC样本的基本多层区域上拍摄最大高脚卵细胞计数,则发现最低样本差异约为10%的最低样本方差。每1000个可见结膜上皮细胞的脚卵细胞数的计数产生接近90(范围36-151)的值,其适度的样品间变异约为30%。三十00x显微镜场和随机采样策略产生542和670个单元格/平方之间的平均GCD值。 mm,但具有至少60%的非常高的内部内和样本方差至少为60%,有时高于100%。 TEM证实了结膜的多层组织和更深的躺脚脚脚脚细胞。除非采用了更具体的策略,否则将roblet细胞计数作为结膜正常性或健康的目标标志物的客观标记可能是高度可变的。除了提供所使用的计数策略的详细信息,提供所使用的实际显微镜场大小的完整细节是非常有用的,以及有关高脚卷细胞计数中的样本内变异性的信息。 (c)2015 Elsevier Ltd.保留所有权利。

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