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钙离子载体A23187诱导的晶状体上皮细胞凋亡促成白内障形成。

Calcimycin-induced lens epithelial cell apoptosis contributes to cataract formation.

作者信息

Li W C, Kuszak J R, Wang G M, Wu Z Q, Spector A

机构信息

Department of Ophthalmology, College of Physicians and Surgeons of Columbia University, New York, NY 10032, USA.

出版信息

Exp Eye Res. 1995 Jul;61(1):91-8. doi: 10.1016/s0014-4835(95)80062-x.

Abstract

Previous studies have shown that calcimycin induces cataract in organ culture. To investigate the mechanism of this induction, the viability of lens epithelial cells in calcimycin (calcium ionophore, A23187)-treated rat lenses were examined. During incubation of lenses with 5 microM calcimycin, apoptotic epithelial cells were found after a 2-hr treatment as determined by terminal deoxynucleotidyl transferase (TdT) labeling. The percentage of apoptotic cells quickly rose as the incubation time increased. After a 12-hr incubation, more than 60% of the lens epithelial cells underwent apoptosis. Prolonged c-fos expression, previously shown to be an indicator of programmed cell death, was also observed during this treatment. DNA fragmentation assays further confirmed that the TdT labeled cells were indeed apoptotic. Under the same incubation conditions, the cultured lenses gradually lost transparency and became completely opaque in about 30 hr. Since the vertebrate lens contains only a single layer of epithelial cells, apoptotic death of these cells activated by calcimycin quickly destroys the lens epithelium, impairs homeostasis of the underlying fiber cells and initiates development of lens opacification.

摘要

先前的研究表明,钙离子载体A23187在器官培养中可诱发白内障。为了探究这种诱发机制,我们检测了经钙离子载体A23187处理的大鼠晶状体中晶状体上皮细胞的活力。在用5微摩尔/升钙离子载体A23187孵育晶状体的过程中,通过末端脱氧核苷酸转移酶(TdT)标记发现,处理2小时后出现了凋亡的上皮细胞。随着孵育时间的延长,凋亡细胞的百分比迅速上升。孵育12小时后,超过60%的晶状体上皮细胞发生凋亡。在此处理过程中还观察到了先前被证明是程序性细胞死亡指标的c-fos表达延长。DNA片段化分析进一步证实,TdT标记的细胞确实发生了凋亡。在相同的孵育条件下,培养的晶状体逐渐失去透明度,并在约30小时内完全变得不透明。由于脊椎动物的晶状体仅含有单层上皮细胞,由钙离子载体A23187激活的这些细胞的凋亡性死亡会迅速破坏晶状体上皮,损害其下方纤维细胞的内环境稳定,并引发晶状体混浊的发展。

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