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糖皮质激素体外对淋巴肉瘤P1798皮质类固醇敏感和耐药细胞系细胞核结构完整性的影响。

Effect of glucocorticoid hormones in vitro on the structural integrity of nuclei in corticosteroid-sensitive and -resistant lines of lymphosarcoma P1798.

作者信息

Nicholson M L, Young D A

出版信息

Cancer Res. 1978 Nov;38(11 Pt 1):3673-80.

PMID:581273
Abstract

Exposure of rat thymus cells to glucocorticoids leads to a decreased ability of nuclei to survive the lysis of whole cells by hypotonic shock. In this study, a similar glucocorticoid-induced increase in "nuclear fragility" was found in both corticoid-sensitive and -resistant lines of P1798 mouse lymphosarcoma cells. In corticoid-sensitive cells a small increase in nuclear fragility is seen after a 2-hr exposure to cortisol (10(-6) M); by 3 hr it is 20 to 40% above control values. This effect appears to be a specific glucocorticoid response. Both cortisol and dexamethasone at 10(-7) M produce an effect, 10(-6) M testosterone is inactive, and cortexolone, which binds to glucocorticoid receptors, reduces the effect. Cycloheximide, at concentrations that inhibit protein synthesis, also blocks this effect. While the corticoid-resistant line also demonstrates an effect of similar magnitude, it requires a much longer exposure to the hormone (6 hr). Distinct differences in the "hardiness" of the two cell lines (nuclei of the corticoid-resistant line are less fragile) measurable in the absence of hormones appears to account for the differential susceptibility to steroids. On this basis a new theory of resistance is advanced where the emergence of resistance is related to structural differences in the cells.

摘要

将大鼠胸腺细胞暴露于糖皮质激素会导致细胞核在低渗休克使全细胞裂解后存活能力下降。在本研究中,在P1798小鼠淋巴肉瘤细胞的皮质激素敏感和抗性细胞系中均发现了类似的糖皮质激素诱导的“核脆性”增加。在皮质激素敏感细胞中,暴露于皮质醇(10⁻⁶ M)2小时后,核脆性略有增加;到3小时时,比对照值高出20%至40%。这种效应似乎是一种特异性糖皮质激素反应。10⁻⁷ M的皮质醇和地塞米松均产生效应,10⁻⁶ M的睾酮无活性,而与糖皮质激素受体结合的皮质酮可降低该效应。抑制蛋白质合成浓度的环己酰亚胺也会阻断这种效应。虽然皮质激素抗性细胞系也表现出类似程度的效应,但它需要更长时间暴露于激素(6小时)。在无激素情况下可测量的两种细胞系“抗性”的明显差异(皮质激素抗性细胞系的细胞核脆性较小)似乎解释了对类固醇的不同敏感性。在此基础上,提出了一种新的抗性理论,即抗性的出现与细胞结构差异有关。

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