Wang Ye, Zang Xinjie, Wang Yao, Chen Peng
State Key Laboratory Cultivation Base, Shandong Eye Institute, Shandong Academy of medical Sciences, Qingdao, China.
Mol Vis. 2012;18:803-15. Epub 2012 Apr 3.
Determine cyclin-dependent kinase inhibitor 2A (p16(Ink4a)) and polycomb ring finger oncogene (Bmi1) expression in corneal endothelium samples from different age groups and test whether the expression of p16(INK4a) and Bmi1 are associated with endothelial cellular senescence in human cornea.
Samples were selected from an eyebank of healthy human corneal endothelial cells (HCECs). Donor human corneas were divided into three age-groups: age ≤30 years, 30-50 years and ≥50 years. The expression of p16(INK4a) and Bmil were analyzed by real-time PCR, immunohistochemistry, and immunofluorescence.
Through real-time PCR, we detected less than threefold decreases in Bmi1 expression and greater than fivefold increases in p16(INK4a) expression associated with aging. Bmi1 expression was significantly down-regulated with increasing donor age. The number of p16(INK4a)-positive cells was significantly higher and the number of Bmi1-positive cells was significantly lower in older donors compared to the younger age groups. Our immunohistochemistry experiments showed that the expression of p16(INK4a) in older donors was stronger than that in younger donors and the expression of Bmi1 in older donors was weaker than that in younger donors. Results from both the immunohistochemistry and real-time PCR experiments confirmed increased expression of p16(INK4a) and decreased expression of Bmi1 with age in HCECs. Additionally, the results of immunofluorescence double-staining for p16(INK4a) and Bmi1 further validated the immunocytochemistry and real-time PCR results.
Our data are the first to demonstrate that high expression of p16(INK4a) and low expression of Bmi1 are associated with endothelial cellular senescence in human cornea. Our findings are not just for cornea transplantation but also for a better understanding of the cornea senescence and the process of aging in this specific human organ.
测定不同年龄组角膜内皮样本中细胞周期蛋白依赖性激酶抑制剂2A(p16(Ink4a))和多梳环指癌基因(Bmi1)的表达,并检测p16(INK4a)和Bmi1的表达是否与人角膜内皮细胞衰老相关。
从健康人角膜内皮细胞(HCECs)眼库中选取样本。供体人角膜分为三个年龄组:年龄≤30岁、30 - 50岁和≥50岁。通过实时PCR、免疫组织化学和免疫荧光分析p16(INK4a)和Bmil的表达。
通过实时PCR,我们检测到与衰老相关的Bmi1表达下降不到三倍,p16(INK4a)表达增加超过五倍。Bmi1表达随供体年龄增加而显著下调。与年轻年龄组相比,老年供体中p16(INK4a)阳性细胞数量显著更高,Bmi1阳性细胞数量显著更低。我们的免疫组织化学实验表明,老年供体中p16(INK4a)的表达强于年轻供体,老年供体中Bmi1的表达弱于年轻供体。免疫组织化学和实时PCR实验结果均证实,HCECs中p16(INK4a)表达随年龄增加而增加,Bmi1表达随年龄增加而降低。此外,p16(INK4a)和Bmi1免疫荧光双染结果进一步验证了免疫细胞化学和实时PCR结果。
我们的数据首次证明,p16(INK4a)的高表达和Bmi1的低表达与人角膜内皮细胞衰老相关。我们的发现不仅适用于角膜移植,还有助于更好地理解角膜衰老以及这个特定人体器官的衰老过程。