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人淋巴细胞中钠钙交换介导的钙内流

Na+/Ca2+ exchange-mediated calcium entry in human lymphocytes.

作者信息

Balasubramanyam M, Rohowsky-Kochan C, Reeves J P, Gardner J P

机构信息

Hypertension Research Center, University of Medicine and Dentistry-New Jersey Medical School, Newark 07103.

出版信息

J Clin Invest. 1994 Nov;94(5):2002-8. doi: 10.1172/JCI117553.

Abstract

Regulation of cytosolic Ca2+ and cytosolic Na+ is critical for lymphocyte cation homeostasis and function. To examine the influence of cytosolic Na+ on Ca2+ regulation in human peripheral blood lymphocytes, Ca2+ entry and cytosolic Ca2+ (measured with fura-2) were monitored in cells in which cytosolic Na+ was increased and/or the Na+ gradient was decreased by reduction of external Na+ concentration. Ouabain-treated cells (0.1 mM for 30 min at 37 degrees C), suspended in Na(+)-free medium, showed a 30-65% increase in Ca2+ uptake compared to cells in 140 mM Na+ medium. Enhanced Ca2+ influx was entirely dependent on ouabain pretreatment and reversal of the Na+ gradient. Na pump inhibition or Na ionophore addition and subsequent exposure to Na(+)-free medium resulted in a sustained elevation of cytosolic Ca2+. As preincubation of cells in Ca(2+)-free medium further enhanced the ouabain-dependent increase in cytosolic Ca2+, the effects of the microsomal Ca(2+)-ATPase inhibitor thapsigargin on Ca2+ influx and cytosolic Ca2+ were studied. Thapsigargin stimulated Ca2+ entry following ouabain pretreatment and reversal of the Na+ gradient; the effects of thapsigargin were retained in the presence of LaCl3, a potent inhibitor of store-dependent calcium influx pathways. These results show lymphocytes demonstrate Na+/Ca2+ exchange activity and suggest the Na+/Ca2+ exchanger modulates cytosolic Ca2+ following intracellular Ca2+ store depletion.

摘要

胞质Ca2+和胞质Na+的调节对于淋巴细胞阳离子稳态和功能至关重要。为了研究胞质Na+对人外周血淋巴细胞中Ca2+调节的影响,在通过降低细胞外Na+浓度使胞质Na+增加和/或Na+梯度降低的细胞中监测Ca2+内流和胞质Ca2+(用fura-2测量)。哇巴因处理的细胞(在37℃下用0.1 mM处理30分钟),悬浮于无Na+培养基中,与在140 mM Na+培养基中的细胞相比,Ca2+摄取增加了30%-65%。增强的Ca2+内流完全依赖于哇巴因预处理和Na+梯度的逆转。钠泵抑制或添加钠离子载体并随后暴露于无Na+培养基导致胞质Ca2+持续升高。由于在无Ca2+培养基中预孵育细胞进一步增强了哇巴因依赖的胞质Ca2+增加,因此研究了微粒体Ca2+-ATP酶抑制剂毒胡萝卜素对Ca2+内流和胞质Ca2+的影响。毒胡萝卜素在哇巴因预处理和Na+梯度逆转后刺激Ca2+内流;在LaCl3(一种有效的储存依赖性钙内流途径抑制剂)存在的情况下,毒胡萝卜素的作用仍然存在。这些结果表明淋巴细胞表现出Na+/Ca2+交换活性,并提示Na+/Ca2+交换器在细胞内Ca2+储存耗竭后调节胞质Ca2+。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca7/294628/0ff1afc5c26d/jcinvest00036-0302-a.jpg

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