Sundaresan Yogapriya, Veerappan Muthukkaruppan, Ramasamy Krishnadas Subbiah, Chidambaranathan Gowri Priya
1Department of Immunology and Stem Cell Biology, Aravind Medical Research Foundation, Madurai, Tamil Nadu India.
2Glaucoma Clinic, Aravind Eye Hospital and Post Graduate Institute of Ophthalmology, Madurai, Tamil Nadu India.
Eye Vis (Lond). 2019 Oct 17;6:31. doi: 10.1186/s40662-019-0156-z. eCollection 2019.
Loss of cells in the human trabecular meshwork (TM) has been reported with ageing and in glaucoma. This study aims to identify, quantify and determine the age-related changes of human TM stem cells (TMSCs).
Isolation of TM cells/ paraffin sectioning was carried out using human corneoscleral rings and whole globes. The TM cells/ sections were immunostained for the stem cell markers ATP-binding cassette protein G2 (ABCG2), nerve growth factor receptor p75 and AnkyrinG (AnkG). Images were acquired using Leica SP8 confocal microscope. The isolated cells were analyzed for two parameters- ABCG2 expression and nucleus to cytoplasmic ratio (N/C ratio). The total number of TM cells and those positive for ABCG2 and p75 in each section were quantified. Spearman rank order correlation was used to determine the association between age and the cell counts.
The TMSCs were identified based on two parameters- high ABCG2 expression and high N/C ratio > 0.7. These stem cells were also positive for p75 and AnkG. The TMSC content based on the two parameters was 21.0 ± 1.4% in < 30 years age group, 12.6 ± 6.6% in 30-60 years and 4.0 ± 3.5% in > 60 years. The stem cells with high ABCG2 and p75 expression were restricted to the Schwalbe's line region of the TM. A significant correlation was observed between the reduction in TMSC content and TM cell count during ageing.
The human TMSCs were identified and quantified based on two parameter analysis. This study established a significant association between age-related reduction in TMSC content and TM cell loss.
据报道,人类小梁网(TM)中的细胞会随着年龄增长以及在青光眼患者中出现丢失。本研究旨在识别、量化并确定人类TM干细胞(TMSCs)与年龄相关的变化。
使用人类角膜巩膜环和全眼球进行TM细胞分离/石蜡切片。对TM细胞/切片进行免疫染色,以检测干细胞标志物ATP结合盒蛋白G2(ABCG2)、神经生长因子受体p75和锚蛋白G(AnkG)。使用徕卡SP8共聚焦显微镜采集图像。对分离出的细胞分析两个参数——ABCG2表达和核质比(N/C比)。对每个切片中TM细胞的总数以及ABCG2和p75阳性的细胞数进行量化。采用Spearman等级相关分析来确定年龄与细胞计数之间的关联。
基于两个参数——高ABCG2表达和高N/C比>0.7来识别TMSCs。这些干细胞对p75和AnkG也呈阳性。基于这两个参数的TMSC含量在<30岁年龄组中为21.0±1.4%,在30 - 60岁组中为12.6±6.6%,在>60岁组中为4.0±3.5%。高ABCG2和p75表达的干细胞局限于TM的施瓦贝线区域。在衰老过程中,观察到TMSC含量的减少与TM细胞计数之间存在显著相关性。
基于双参数分析对人类TMSCs进行了识别和量化。本研究确立了TMSC含量与年龄相关的减少和TM细胞丢失之间的显著关联。