Suppr超能文献

一种平滑肌样细胞系中的pH调节转运系统。

pH regulatory transport systems in a smooth muscle-like cell line.

作者信息

Putnam R W

机构信息

Department of Physiology and Biophysics, Wright State University School of Medicine, Dayton, Ohio 45401.

出版信息

Am J Physiol. 1990 Mar;258(3 Pt 1):C470-9. doi: 10.1152/ajpcell.1990.258.3.C470.

Abstract

The membrane transport systems responsible for pH regulation in BC3H-1 cells were studied using the pH-sensitive fluorescent dye 2',7'-bis(2-carboxyethyl)-5,6-carboxyfluorescein (BCECF). In nominally CO2-free Na N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid buffer (NHB) recovery from acidification after an NH4Cl pulse was reversibly inhibited by 1 mM amiloride or by Na-free solutions. On exposure to 5% CO2-HCO3 (external pH constant at 7.4), BC3H-1 cells alkalinized by approximately 0.3-0.4 pH unit. This CO2-induced alkalinization was unaffected by 1 mM amiloride, markedly reduced by 0.5 mM 4-acetamido-4'-isothiocyanostilbene-2,2'-disulfonic acid (SITS), and inhibited by Na-free solutions. On readdition of Na, cells rapidly alkalinized, even in the presence of 1 mM amiloride. Exposure to Cl-free CO2-HCO3 solutions caused a rapid alkalinization of nearly 1 pH unit that was abolished by SITS, largely independent of Na, unaffected by amiloride, and unchanged by membrane depolarization in high external K solutions. CO2-induced alkalinization was slowed by approximately 75% after prolonged exposure of cells to Cl-free NHB, but a distinct recovery from acidification remained in these Cl-depleted cells. This recovery was Na-dependent, SITS-inhibitable, and unaffected by depolarization in high-K solutions. In the presence of CO2, the acidification seen in response to NH4Cl-induced alkalinization was reduced 50% by 0.5 mM SITS. These data suggest that the regulation of pH in BC3H-1 cells is mediated by at least three transport systems: 1) Na-H exchange; 2) Cl-HCO3 exchange; and 3) electroneutral (Na + HCO3)-Cl exchange.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用对pH敏感的荧光染料2',7'-双(2-羧乙基)-5,6-羧基荧光素(BCECF)研究了负责BC3H-1细胞pH调节的膜转运系统。在名义上无CO2的N-2-羟乙基哌嗪-N'-2-乙磺酸缓冲液(NHB)中,NH4Cl脉冲后酸化的恢复可被1 mM氨氯吡脒或无钠溶液可逆抑制。暴露于5% CO2-HCO3(外部pH恒定在7.4)时,BC3H-1细胞碱化约0.3-0.4个pH单位。这种CO2诱导的碱化不受1 mM氨氯吡脒的影响,被0.5 mM 4-乙酰氨基-4'-异硫氰酸基芪-2,2'-二磺酸(SITS)显著降低,并被无钠溶液抑制。重新添加钠后,即使存在1 mM氨氯吡脒,细胞也会迅速碱化。暴露于无氯的CO2-HCO3溶液会导致近1个pH单位的快速碱化,这被SITS消除,很大程度上与钠无关,不受氨氯吡脒影响,且在高外部钾溶液中膜去极化时不变。细胞长时间暴露于无氯的NHB后,CO2诱导的碱化减慢约75%,但这些氯耗竭细胞中仍有明显的酸化恢复。这种恢复依赖于钠,可被SITS抑制,且不受高钾溶液中去极化的影响。在有CO2存在的情况下,0.5 mM SITS可使NH4Cl诱导的碱化所导致的酸化降低50%。这些数据表明,BC3H-1细胞中pH的调节至少由三种转运系统介导:1)钠-氢交换;2)氯-碳酸氢根交换;3)电中性(钠+碳酸氢根)-氯交换。(摘要截断于250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验