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氯化钠和尿素的组合可提高内髓集合管(IMCD)细胞在高渗环境下的存活率。

A combination of NaCl and urea enhances survival of IMCD cells to hyperosmolality.

作者信息

Santos B C, Chevaile A, Hébert M J, Zagajeski J, Gullans S R

机构信息

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.

出版信息

Am J Physiol. 1998 Jun;274(6):F1167-73. doi: 10.1152/ajprenal.1998.274.6.F1167.

Abstract

Physiological adaptation to the hyperosmolar milieu of the renal medulla involves a complex series of signaling and gene expression events in which NaCl and urea activate different cellular processes. In the present study, we evaluated the effects of NaCl and urea, individually and in combination, on the viability of murine inner medullary collecting duct (mIMCD3) cells. Exposure to hyperosmolar NaCl or urea caused comparable dose- and time-dependent decreases in cell viability, such that 700 mosmol/kgH2O killed >90% of the cells within 24 h. In both cases, cell death was an apoptotic event. For NaCl, loss of viability at 24 h paralleled decreases in RNA and protein synthesis at 4h, whereas lethal doses of urea had little or no effect on these biosynthetic processes. Cell cycle analysis showed both solutes caused a slowing of the G2/M phase. Surprisingly, cells exposed to a combination of NaCl + urea were significantly more osmotolerant such that 40% survived 900 mosmol/kgH2O. Madin-Darby canine kidney cells but not human umbilical vein endothelial cells also exhibited a similar osmotolerance response. Enhanced survival was not associated with a restoration of normal biosynthetic rates or cell cycle progression. However, the combination of NaCl + urea resulted in a shift in Hsp70 expression that appeared to correlate with survival. In conclusion, hyperosmolar NaCl and urea activate independent and complementary cellular programs that confer enhanced osmotolerance to renal medullary epithelial cells.

摘要

对肾髓质高渗环境的生理适应涉及一系列复杂的信号传导和基因表达事件,其中氯化钠和尿素激活不同的细胞过程。在本研究中,我们评估了氯化钠和尿素单独及联合作用对小鼠髓质内集合管(mIMCD3)细胞活力的影响。暴露于高渗氯化钠或尿素会导致细胞活力出现类似的剂量和时间依赖性下降,以至于700毫渗摩尔/千克H₂O在24小时内杀死了>90%的细胞。在这两种情况下,细胞死亡都是凋亡事件。对于氯化钠,24小时时活力的丧失与4小时时RNA和蛋白质合成的下降平行,而致死剂量的尿素对这些生物合成过程几乎没有影响。细胞周期分析表明,两种溶质都会导致G2/M期的减缓。令人惊讶的是,暴露于氯化钠+尿素组合的细胞对渗透压的耐受性明显更高,以至于40%的细胞在900毫渗摩尔/千克H₂O下存活。Madin-Darby犬肾细胞而非人脐静脉内皮细胞也表现出类似的渗透压耐受性反应。存活率的提高与正常生物合成速率或细胞周期进程的恢复无关。然而,氯化钠+尿素的组合导致热休克蛋白70(Hsp70)表达发生变化,这似乎与存活率相关。总之,高渗氯化钠和尿素激活了独立且互补的细胞程序,从而赋予肾髓质上皮细胞更高的渗透压耐受性。

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