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视网膜切片的形态计量分析。

Morphometric analyses of retinal sections.

作者信息

Chan Tin Fung, Chiu Kin, Lok Carmen Ka Ming, Lau Ho Wing, So Kwok-Fai, Chang Raymond Chuen-Chung

机构信息

Laboratory of Neurodegenerative Diseases, Department of Anatomy, LKS Faculty of Medicine, The University of Hong Kong.

出版信息

J Vis Exp. 2012 Feb 19(60):3377. doi: 10.3791/3377.

Abstract

Morphometric analyses of retinal sections have been used in examining retinal diseases. For examples, neuronal cells were significantly lost in the retinal ganglion cell layer (RGCL) in rat models with N-methyl-D-aspartate (NMDA)-induced excitotoxicity(1), retinal ischemia-reperfusion injury(2) and glaucoma(3). Reduction of INL and inner plexiform layer (IPL) thicknesses were reversed with citicoline treatment in rats' eyes subjected to kainic acid-mediated glutamate excitotoxicity(4). Alteration of RGC density and soma sizes were observed with different drug treatments in eyes with elevated intraocular pressure(3,5,6). Therefore, having objective methods of analyzing the retinal morphometries may be of great significance in evaluating retinal pathologies and the effectiveness of therapeutic strategies. The retinal structure is multi-layers and several different kinds of neurons exist in the retina. The morphometric parameters of retina such as cell number, cell size and thickness of different layers are more complex than the cell culture system. Early on, these parameters can be detected using other commercial imaging software. The values are normally of relative value, and changing to the precise value may need further accurate calculation. Also, the tracing of the cell size and morphology may not be accurate and sensitive enough for statistic analysis, especially in the chronic glaucoma model. The measurements used in this protocol provided a more precise and easy way. And the absolute length of the line and size of the cell can be reported directly and easy to be copied to other files. For example, we traced the margin of the inner and outer most nuclei in the INL and formed a line then using the software to draw a 90 degree angle to measure the thickness. While without the help of the software, the line maybe oblique and the changing of retinal thickness may not be repeatable among individual observers. In addition, the number and density of RGCs can also be quantified. This protocol successfully decreases the variability in quantitating features of the retina, increases the sensitivity in detecting minimal changes. This video will demonstrate three types of morphometric analyses of the retinal sections. They include measuring the INL thickness, quantifying the number of RGCs and measuring the sizes of RGCs in absolute value. These three analyses are carried out with Stereo Investigator (MBF Bioscience - MicroBrightField, Inc.). The technique can offer a simple but scientific platform for morphometric analyses.

摘要

视网膜切片的形态计量分析已被用于研究视网膜疾病。例如,在N-甲基-D-天冬氨酸(NMDA)诱导的兴奋性毒性大鼠模型(1)、视网膜缺血再灌注损伤模型(2)和青光眼模型(3)中,视网膜神经节细胞层(RGCL)中的神经元细胞显著丢失。在 kainic 酸介导的谷氨酸兴奋性毒性作用下的大鼠眼中,用胞磷胆碱治疗可逆转内核层(INL)和内网状层(IPL)厚度的减少(4)。在眼压升高的眼中,不同药物治疗观察到视网膜神经节细胞(RGC)密度和胞体大小的改变(3,5,6)。因此,拥有客观分析视网膜形态计量的方法对于评估视网膜病变和治疗策略的有效性可能具有重要意义。视网膜结构是多层的,视网膜中存在几种不同类型的神经元。视网膜的形态计量参数,如细胞数量、细胞大小和不同层的厚度,比细胞培养系统更复杂。早期,可以使用其他商业成像软件检测这些参数。这些值通常是相对值,要得到精确值可能需要进一步精确计算。此外,细胞大小和形态的追踪对于统计分析可能不够准确和灵敏,尤其是在慢性青光眼模型中。本方案中使用的测量方法提供了一种更精确、简便的方法。并且可以直接报告线的绝对长度和细胞大小,并且易于复制到其他文件中。例如,我们追踪 INL 中最内层和最外层细胞核的边缘并形成一条线,然后使用软件绘制一个 90 度角来测量厚度。如果没有软件的帮助,这条线可能是倾斜的,并且不同观察者之间视网膜厚度的变化可能不可重复。此外,RGC 的数量和密度也可以进行量化。本方案成功降低了视网膜定量特征的变异性,提高了检测微小变化的灵敏度。本视频将展示视网膜切片的三种形态计量分析类型。它们包括测量 INL 厚度、量化 RGC 的数量以及以绝对值测量 RGC 的大小。这三种分析是使用 Stereo Investigator(MBF Bioscience - MicroBrightField, Inc.)进行的。该技术可为形态计量分析提供一个简单但科学的平台。

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