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首页> 外文期刊>Ophthalmology >Distribution of precursors in human corneal stromal cells and endothelial cells.
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Distribution of precursors in human corneal stromal cells and endothelial cells.

机译:前体在人角膜基质细胞和内皮细胞中的分布。

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摘要

PURPOSE: We identified original tissue-committed precursors with limited self-renewal capacity from human corneal stromal (HCS) cells and human corneal endothelial (HCE) cells, then tried to determine the distribution and proliferative capacity of the precursors. DESIGN: Experimental study. PARTICIPANTS: Eighteen human corneas from donors 56 to 68 years old. METHODS: Human corneal stromal cells were divided into groups based on distance from the center of the cornea: <6 mm (central), 6 to 8 mm (paracentral), and 8 to 10 mm (peripheral). Human corneal endothelial cells were separated into 2 groups: <7.5 mm (central) and 7.5 to 10 mm (peripheral) from the center. Each group was subjected to the sphere-forming assay using serum-free medium containing growth factors in floating culture. Sphere numbers and the proliferative capacity of spheres in adherent culture were compared among the groups. MAIN OUTCOME MEASURES: Density and proliferative capacity of precursors from each area of HCS and HCE cells. RESULTS: Primary spheres were isolated from all groups of HCS and HCE cells. The rate of primary sphere formation from peripheral HCS cells was higher than those of the other 2 groups, being 1.5-fold greater than in the paracentral cornea and 4-fold greater than in the central cornea. The rate of primary sphere formation by peripheral HCE cells was significantly higher than that by central HCE cells, being 4-fold greater than in the central cornea. There were no differences in the proliferative capacity of HCS and HCE cell spheres from the different areas after adherent culture. CONCLUSIONS: All HCS and HCE cells contain a significant number of precursors, but the peripheral cells have a density of precursors higher than that of the central cells. Precursors from each area do not show differences of proliferative capacity. Our findings may in part explain changes after excimer laser treatment and may have implications for corneal transplantation procedures.
机译:目的:我们从人角膜基质(HCS)细胞和人角膜内皮(HCE)细胞中鉴定出具有自我更新能力有限的原始组织定型前体,然后尝试确定前体的分布和增殖能力。设计:实验研究。参与者:年龄在56至68岁之间的18个人类角膜。方法:根据距角膜中心的距离,将人类角膜基质细胞分为以下几组:<6 mm(中心),6至8 mm(中心旁)和8至10 mm(外围)。将人角膜内皮细胞分为两组:距中心<7.5 mm(中心)和7.5至10 mm(外围)。使用漂浮培养中含有生长因子的无血清培养基对每组进行球形成测定。比较各组在贴壁培养中的球数和球的增殖能力。主要观察指标:HCS和HCE细胞各个区域的前体的密度和增殖能力。结果:从所有HCS和HCE细胞组中分离出原球。来自周围HCS细胞的初级球形成速率高于其他两组,比中央旁角膜高1.5倍,比中央角膜高4倍。外周HCE细胞形成初级球的速率显着高于中央HCE细胞,是中央角膜的4倍。贴壁培养后,来自不同区域的HCS和HCE细胞球的增殖能力没有差异。结论:所有HCS和HCE细胞均含有大量前体,但外周细胞的前体密度高于中央细胞。每个区域的前体均未显示出增殖能力的差异。我们的发现可能部分解释了准分子激光治疗后的变化,可能对角膜移植手术有影响。

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