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一种测定小鼠晶状体未受干扰上皮细胞数量的方法。

A method for determining cell number in the undisturbed epithelium of the mouse lens.

作者信息

Bassnett Steven, Shi Yanrong

机构信息

Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO 63117, USA.

出版信息

Mol Vis. 2010 Nov 4;16:2294-300.

Abstract

The anterior face of the mouse lens is covered by a layer of epithelial cells. The epithelial cells serve a barrier function at the lens surface and as a progenitor population from which lens fiber cells, the predominant cell type of the lens, are derived. Decreased epithelial cell density is commonly observed during aging and cataract formation in humans and animal models and may contribute directly to tissue opacification. However, the loss of cells from the epithelium is often not easy to quantify, in part because the cells are arrayed across a near-spherical surface and, as a consequence, are difficult to image and count. Here, we describe a technique for determining epithelial cell number in the undisturbed lens of the mouse, a popular cataract model. The method utilizes orthographic projections of confocal images collected from the anterior and equatorial regions of the lens. The overlapping projections are brought into register using the unique distribution of proliferating cells as fiduciary points. Cell counts are performed using a computer-assisted method. This approach offers several advantages over flat-mount methods employed previously.

摘要

小鼠晶状体的前表面覆盖着一层上皮细胞。上皮细胞在晶状体表面起屏障作用,并作为祖细胞群体,晶状体的主要细胞类型——晶状体纤维细胞由此衍生而来。在人类和动物模型的衰老及白内障形成过程中,上皮细胞密度通常会降低,这可能直接导致组织混浊。然而,上皮细胞的丢失往往不易量化,部分原因是这些细胞排列在近乎球形的表面上,因此难以成像和计数。在此,我们描述了一种用于确定小鼠(一种常用的白内障模型)未受干扰的晶状体中上皮细胞数量的技术。该方法利用从晶状体前区和赤道区收集的共聚焦图像的正射投影。利用增殖细胞的独特分布作为基准点,使重叠投影对齐。使用计算机辅助方法进行细胞计数。与先前采用的平铺法相比,这种方法具有几个优点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea4b/2997765/6a8102d0bf1f/mv-v16-2294-f1.jpg

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