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制霉菌素刺激红细胞细胞膜乱序。

Stimulation of erythrocyte cell membrane scrambling by nystatin.

机构信息

Department of Physiology, University of Tuebingen, Tuebingen, Germany.

出版信息

Basic Clin Pharmacol Toxicol. 2015 Jan;116(1):47-52. doi: 10.1111/bcpt.12279. Epub 2014 Jul 4.

Abstract

The antifungal ionophore nystatin dissipates the Na(+) and K(+) gradients across the cell membrane, leading to cellular gain of Na(+) and cellular loss of K(+) . The increase of cellular Na(+) concentration may result in Ca(2+) accumulation in exchange for Na(+) . Increase of cytosolic Ca(2+) activity ([Ca(2+) ]i ) and loss of cellular K(+) foster apoptosis-like suicidal erythrocyte death or eryptosis, which is characterised by cell shrinkage and cell membrane scrambling leading to phosphatidylserine exposure at the erythrocyte surface. The present study explored whether nystatin stimulates eryptosis. Cell volume was estimated from forward scatter (FSC), phosphatidylserine exposure from annexin V binding and [Ca(2+) ]i from Fluo3-fluorescence in flow cytometry. A 48-hr exposure to nystatin (15 μg/ml) was followed by a significant increase of [Ca(2+) ]i , a significant increase of annexin V binding and a significant decrease of FSC. The annexin V binding after nystatin treatment was significantly blunted in the nominal absence of extracellular Ca(2+) . Partial replacement of extracellular Na(+) with extracellular K(+) blunted the nystatin-induced erythrocyte shrinkage but increased [Ca(2+) ]i and annexin V binding. Nystatin triggers cell membrane scrambling, an effect at least partially due to entry of extracellular Ca(2+) .

摘要

抗真菌离子载体制霉菌素会耗散跨细胞膜的 Na(+) 和 K(+) 梯度,导致细胞内 Na(+) 增加和 K(+) 丢失。细胞内 Na(+) 浓度的增加可能导致 Ca(2+) 以交换 Na(+) 的形式积累。细胞质 Ca(2+) 活性增加([Ca(2+) ]i)和细胞内 K(+) 的丢失促进类似凋亡的红细胞自杀性死亡或红细胞皱缩,其特征是细胞体积缩小和细胞膜无序排列,导致磷脂酰丝氨酸在红细胞表面暴露。本研究探讨了制霉菌素是否刺激红细胞皱缩。通过流式细胞术从前向散射(FSC)估计细胞体积,从 annexin V 结合估计磷脂酰丝氨酸暴露,从 Fluo3-荧光估计 [Ca(2+) ]i。制霉菌素(15 μg/ml)孵育 48 小时后,[Ca(2+) ]i 显著增加,annexin V 结合显著增加,FSC 显著降低。在不存在细胞外 Ca(2+)的情况下,制霉菌素处理后的 annexin V 结合显著减弱。用细胞外 K(+)部分替代细胞外 Na(+) 可减轻制霉菌素诱导的红细胞皱缩,但增加 [Ca(2+) ]i 和 annexin V 结合。制霉菌素触发细胞膜无序排列,这种作用至少部分是由于细胞外 Ca(2+) 的进入。

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