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首页> 外文期刊>British Journal of Cancer >Mode of cell death induced in human lymphoid cells by high and low doses of glucocorticoid
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Mode of cell death induced in human lymphoid cells by high and low doses of glucocorticoid

机译:高和低剂量糖皮质激素诱导人淋巴样细胞死亡的模式

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摘要

The kinetics, specificity and morphology of cytolethal responses have been studied in human glucocorticoid-sensitive and -insensitive lymphoid cell lines (HLCL) and fibroblasts following treatment with high (10(-3)M) and low (10(-6)M) doses of steroid. The high dose cytolethal response appears non-specific occurring in all cell lines with every steroid tested. By contrast, the low dose (pharmacological) cytolethal response requires an active glucocorticoid and a sensitive HLCL. However, both high and low concentrations of steroid induce virtually identical morphological changes in dying cells and similar changes can be induced in cells killed by deliberate feed exhaustion. Although the morphological features in each case resemble apoptosis, the "programmed" physiological form of cell death, the intracellular events leading to cytolysis seem likely to differ. The earliest morphological changes presaging cell death comprise rounding up of cells and condensation of nuclear chromatin. Nuclear changes progress rapidly thereafter and appear to result from detachment of chromatin from the nuclear matrix. The low dose cytolethal response requires the continuous presence of glucocorticoid for periods in excess of 24h, prior to which cell growth appears unaffected. The constancy of this latent interval suggests glucocorticoids may influence some replication control mechanism unrelated initially to macromolecular biosynthesis.
机译:在高(10(-3)M)和低(10(-6)M)处理后,已在人糖皮质激素敏感性和非敏感性淋巴样细胞系(HLCL)和成纤维细胞中研究了细胞致死反应的动力学,特异性和形态。剂量的类固醇。高剂量的细胞致死反应似乎在所有测试类固醇的所有细胞系中均非特异性发生。相反,低剂量(药理)细胞致死反应需要活性糖皮质激素和敏感的HLCL。但是,高浓度和低浓度的类固醇都会在垂死的细胞中诱导出几乎相同的形态变化,而在故意饲料耗尽而杀死的细胞中也可以诱导出相似的变化。尽管每种情况下的形态特征都类似于细胞凋亡,细胞死亡的“程序化”生理形式,但导致细胞溶解的细胞内事件似乎可能有所不同。促使细胞死亡的最早形态变化包括细胞聚集和核染色质浓缩。此后,核变化迅速发展,似乎是由于染色质从核基质上脱离所致。低剂量的细胞致死反应要求糖皮质激素持续存在超过24小时,然后细胞生长似乎不受影响。该潜伏期的恒定性表明糖皮质激素可能影响某些与大分子生物合成无关的复制控制机制。

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