Corasanti J G, Gleeson D, Boyer J L
Department of Medicine and Liver Center, Yale University School of Medicine, New Haven, Connecticut 06510.
Am J Physiol. 1990 Feb;258(2 Pt 1):G290-8. doi: 10.1152/ajpgi.1990.258.2.G290.
Isolated hepatocyte suspensions were exposed to hypotonic and hypertonic stresses and serial cell volume measurements were made with an electronic particle size analyzer. With the exposure to hypotonic (160 mosM) buffer, hepatocytes swelled within 30-60 s as osomometers [relative volume (RV) = 1.44 +/- 0.08] and subsequently underwent regulatory volume decrease (RVD) back toward the resting (isotonic) level (1.16 +/- 0.05). This volume recovery was blocked by 65 mM extracellular K+ concentration and inhibited by barium (1 mM) and quinine (0.5 mM) but not by bumetanide (0.1 mM). Chloride depletion inhibited RVD by approximately 40% while 0.5 mM 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid (DIDS) blocked the recovery by almost 90%. Calcium deprivation had no effect on RVD, nor did ouabain, amiloride, or sodium replacement. When exposed to buffer made hypertonic by addition of 200 mM sucrose, cells shrunk as osmometers (RV = 0.74 +/- 0.02) but did not exhibit regulatory volume increase (RVI). However, when cells that had first undergone RVD were reexposed to isotonic medium (relative hypertonic stress) RVI could be demonstrated from RV 0.77 +/- 0.17 to 0.91 +/- 0.20. This response was dependent on sodium, partially dependent on bicarbonate and chloride, and inhibited by the Na(+)-H+ exchange inhibitor amiloride (1 mM) but not by DIDS. Our findings suggest that RVD in rat hepatocytes is mediated by quinine- and barium-sensitive K+ conductance and DIDS-sensitive anion conductance, which is partly accounted for by Cl-; RVI is mediated by activation of Na(+)-H+ exchange coupled with a bicarbonate- and chloride-dependent but DIDS-insensitive process.
将分离的肝细胞悬液暴露于低渗和高渗应激环境中,并用电子粒度分析仪进行连续的细胞体积测量。当暴露于低渗(160 mosM)缓冲液时,肝细胞在30 - 60秒内膨胀,如同渗透计一样(相对体积(RV)= 1.44 ± 0.08),随后经历调节性体积减小(RVD),恢复到静息(等渗)水平(1.16 ± 0.05)。细胞外钾离子浓度为65 mM时可阻断这种体积恢复,钡(1 mM)和奎宁(0.5 mM)可抑制该过程,但布美他尼(0.1 mM)无此作用。氯离子缺失可使RVD抑制约40%,而0.5 mM 4,4'-二异硫氰基芪-2,2'-二磺酸(DIDS)可使恢复过程几乎完全阻断达90%。钙缺失对RVD无影响,哇巴因、氨氯吡咪或钠替代也无影响。当暴露于添加200 mM蔗糖而变为高渗的缓冲液中时,细胞如同渗透计一样收缩(RV = 0.74 ± 0.02),但未表现出调节性体积增加(RVI)。然而,当首先经历RVD的细胞重新暴露于等渗培养基(相对高渗应激)时,RVI可表现为从RV 0.77 ± 0.17增加到0.91 ± 0.20。这种反应依赖于钠,部分依赖于碳酸氢根和氯离子,并被钠氢交换抑制剂氨氯吡咪(1 mM)抑制,但不受DIDS抑制。我们的研究结果表明,大鼠肝细胞中的RVD由奎宁和钡敏感的钾离子电导以及DIDS敏感的阴离子电导介导,部分由氯离子介导;RVI由钠氢交换激活介导,同时伴有一个依赖于碳酸氢根和氯离子但对DIDS不敏感的过程。