Jarrin Miguel, Mansergh Fiona C, Boulton Michael E, Gunhaga Lena, Wride Michael A
Visual Neuroscience and Molecular Biology Research Group, School of Optometry and Vision Sciences, Cardiff, University, Cardiff, Wales, UK.
Mol Vis. 2012;18:2758-69. Epub 2012 Nov 22.
Survivin (Birc5) is the smallest member of the inhibitor of apoptosis (IAP) protein family, which regulates the cell cycle/apoptosis balance. The purpose of this study was to examine Survivin expression in the embryonic chick lens, in chick lens epithelial cell cultures, and in the postnatal mouse lens.
Survivin expression was examined using a combination of quantitative real-time polymerase chain reaction, western blotting, and immunocytochemistry. To correlate Survivin expression with the timing of proliferation, we determined the profile of cell proliferation in the developing lens using the cell cycle marker proliferating cell nuclear antigen (PCNA) in quantitative western blotting and immunocytochemistry studies. We also examined the expression of PCNA and the extent of denucleation using terminal deoxynucleotidyl transferase (TdT)-mediated biotin-dUTP nick-end labeling (TUNEL) of lentoids (lens fiber-like cells) during chick lens epithelial cell differentiation in vitro.
At embryonic day (ED) 4, Survivin immunostaining was present in two pools in lens epithelial cells and fiber cells: cytoplasmic and nuclear. The nuclear staining became more pronounced as the lens epithelial cells differentiated into lens fiber cells. At ED12, Survivin staining was observed in lens fiber cell nuclei containing marginalized chromatin, indicative of early denucleation events. Using western blotting, Survivin expression peaked at ED6, diminishing thereafter. This profile of expression correlated with the events in chick lens epithelial cell cultures: i) increased Survivin expression was associated with an increase in PCNA staining up to day 6 of culture and ii) downregulation of Survivin expression at day 8 of culture was coincident with a dramatic decrease in PCNA staining and an increase in TdT-mediated biotin-dUTP nick-end labeling in lentoids. In early postnatal mouse lenses, Survivin and PCNA were highly expressed and decreased thereafter during postnatal lens maturation.
Survivin is expressed during chick and mouse lens development and in chick lens epithelial cell cultures. High levels of Survivin expression correlated with high rates of proliferation of lens epithelial cells at early stages of development. Downregulation of Survivin expression with development and its progressive localization to the nuclei of lens fiber cells was coincident with a decrease in cell proliferation and increased denucleation in differentiating lens fiber cells. These studies suggest an important role for Survivin as a dual regulator of lens epithelial cell proliferation and lens fiber cell differentiation.
生存素(Birc5)是凋亡抑制蛋白(IAP)家族中最小的成员,可调节细胞周期/凋亡平衡。本研究旨在检测生存素在胚胎期鸡晶状体、鸡晶状体上皮细胞培养物及出生后小鼠晶状体中的表达情况。
采用定量实时聚合酶链反应、蛋白质印迹法和免疫细胞化学相结合的方法检测生存素的表达。为了将生存素表达与增殖时间相关联,我们在定量蛋白质印迹法和免疫细胞化学研究中,使用细胞周期标记物增殖细胞核抗原(PCNA)来确定发育中晶状体的细胞增殖情况。我们还在体外鸡晶状体上皮细胞分化过程中,利用末端脱氧核苷酸转移酶(TdT)介导的生物素-dUTP缺口末端标记(TUNEL)检测了类晶状体(晶状体纤维样细胞)中PCNA的表达及去核程度。
在胚胎第4天(ED4),生存素免疫染色在晶状体上皮细胞和纤维细胞中有两个分布区域:细胞质和细胞核。随着晶状体上皮细胞分化为晶状体纤维细胞,细胞核染色变得更加明显。在ED12时,在含有边缘化染色质的晶状体纤维细胞核中观察到生存素染色,这表明早期去核事件。通过蛋白质印迹法检测,生存素表达在ED6时达到峰值,此后逐渐下降。这种表达模式与鸡晶状体上皮细胞培养中的情况相关:i)在培养至第6天前,生存素表达增加与PCNA染色增加相关;ii)在培养第8天时,生存素表达下调与PCNA染色显著减少以及类晶状体中TdT介导的生物素-dUTP缺口末端标记增加同时出现。在出生后早期小鼠晶状体中,生存素和PCNA高度表达,随后在出生后晶状体成熟过程中下降。
生存素在鸡和小鼠晶状体发育过程以及鸡晶状体上皮细胞培养中均有表达。高水平的生存素表达与发育早期晶状体上皮细胞高增殖率相关。随着发育,生存素表达下调及其逐渐定位于晶状体纤维细胞核,这与分化中的晶状体纤维细胞增殖减少和去核增加同时发生。这些研究表明生存素作为晶状体上皮细胞增殖和晶状体纤维细胞分化的双重调节因子具有重要作用。