Shimmura S, Ishioka M, Hanada K, Shimazaki J, Tsubota K
Department of Ophthalmology, Tokyo Dental College, Chiba, Japan.
Invest Ophthalmol Vis Sci. 2000 May;41(6):1364-9.
To investigate tolomerase activity and p53 expression in pterygial tissue.
Pterygia tissue was obtained during excisional surgery fr om 35 eyes of 35 patients, and superior bulbar conjunctival tissue from the same eye was also sampled as control when possible. Fluorescence telomeric repeat amplification protocol was used to measure telomerase activity in whole pterygium samples from 9 cases and in the epithelium and stroma of pterygium from another 10 cases. p53 protein content was measured by enzyme-linked immunosorbent assay (ELISA) in tissues obtained from 7 eyes, as well as in epithelial cell suspensions collected by brush cytology in 8 eyes. Six samples were also analyzed for UV-specific mutations in the p53 gene by the single-strand conformation polymorphism technique and DNA sequencing. A conjunctival epithelial cell line was irradiated with sublethal levels of UV-B to investigate whether telomerase activity can be induced in vitro.
In all, 63% of pterygia samples demonstrated telomerase activity, whereas all 10 paired conjunctival control samples were negative (P = 0.05, chi-square test). Of the 10 samples in which telomerase activity was measured separately in the epithelium and stroma of pterygia, 5 samples were positive in the epithelium, only 1 of which had activity in the stroma. Average telomerase activity in positive samples was 18.44 +/- 8.77 U/microg protein, compared with telomerase activity measured in a carcinoma in situ patient (33.73 U/microg), and in an immortalized conjunctival epithelial cell line (50.72 +/- 15.55 U/microg). Telomerase activity was not upregulated in this cell line by UV-B exposure. All 6 pterygia samples tested for p53 mutations did not reveal the UV-specific mutations in exons 5, 6, 7, or 8. No statistical significance was observed in the pterygium or conjunctiva p53 protein levels in epithelial cells collected by brush cytology, while p53 protein level was lower in pterygia when measured in whole tissue samples.
Telomerase activity was detected in some pterygia, mostly in the epithelium. Pterygia was not associated with an increase in epithelial p53 protein content measured by ELISA.
研究翼状胬肉组织中的端粒酶活性及p53表达。
从35例患者的35只眼中获取翼状胬肉组织,尽可能同时采集同一只眼的上方球结膜组织作为对照。采用荧光端粒重复序列扩增法检测9例翼状胬肉全组织样本以及另外10例翼状胬肉上皮和基质中的端粒酶活性。通过酶联免疫吸附测定(ELISA)法检测7只眼组织中的p53蛋白含量,以及通过刷片细胞学收集的8只眼上皮细胞悬液中的p53蛋白含量。还采用单链构象多态性技术和DNA测序对6个样本的p53基因紫外线特异性突变进行分析。用亚致死剂量的UV-B照射结膜上皮细胞系,以研究体外能否诱导端粒酶活性。
总体而言,63%的翼状胬肉样本显示端粒酶活性,而所有10对结膜对照样本均为阴性(P = 0.05,卡方检验)。在10个分别检测翼状胬肉上皮和基质端粒酶活性的样本中,5个上皮样本呈阳性,其中只有1个基质样本有活性。阳性样本的平均端粒酶活性为18.44±8.77 U/μg蛋白,与原位癌患者(33.73 U/μg)和永生化结膜上皮细胞系(50.72±15.55 U/μg)中测得的端粒酶活性相比。UV-B照射未使该细胞系中的端粒酶活性上调。所有6个检测p53突变的翼状胬肉样本均未发现外显子5、6、7或外显子8中的紫外线特异性突变。通过刷片细胞学收集的上皮细胞中,翼状胬肉或结膜的p53蛋白水平无统计学意义,而在全组织样本中测量时,翼状胬肉中的p53蛋白水平较低。
在部分翼状胬肉中检测到端粒酶活性,主要在上皮中。ELISA法检测显示翼状胬肉与上皮p53蛋白含量增加无关。