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Hep G2细胞中的细胞内pH调节:表皮生长因子、转化生长因子-α和胰岛素样生长因子-II对Na+/H+交换活性的影响。

Intracellular pH regulation in Hep G2 cells: effects of epidermal growth factor, transforming growth factor-alpha, and insulinlike growth factor-II on Na+/H+ exchange activity.

作者信息

Strazzabosco M, Poci C, Spirlì C, Zsembery A, Granato A, Massimino M L, Crepaldi G

机构信息

Istituto di Medicina Interna, Università di Padova, Italy.

出版信息

Hepatology. 1995 Aug;22(2):588-97.

PMID:7635429
Abstract

Intracellular pH (pHi) plays an important role in the metabolic activation of quiescent cells after a proliferative stimulus, and Na+/H+ exchange activity is required for growth in some extrahepatic tumors. To investigate intracellular acid/base homeostasis in hepatoma cells and the effects of putative liver growth factors on Na+/h+ exchange activity, we have studied intracellular pH (pHi) regulation in Hep G2 cells, a well-differentiated hepatoma cell line, both in resting conditions and after administration of epidermal growth factor (EGF), transforming growth factor-alpha (TGF alpha), and insulinlike growth factor-II (IGF-II). The effects of fetal calf serum, TGF alpha, and amiloride on 3H-Thymidine incorporation were also studied. Amiloride (1 mmol/L) and external Na+ removal decreased baseline pHi in both HEPES and KRB. In HEPES, cells recovered from an acid load (20 mmol/L NH4Cl) by an amiloride inhibitable Na+/H+ exchange. In KRB, an additional, DIDS-inhibitable, Na(+)- and HCO3- dependent, but Cl(-)-independent acid extruder (Na:HCO3 cotransport) was activated. No evidence was found for a Cl/HCO3 exchange acting as acid loader. Administration of EGF and TGF alpha, but not of IGF-II, induced a dose-dependent, amiloride-inhibitable increase in baseline pHi, together with an increase in Na+/H+ exchange activity, shifting to the right the JH/pHi curve. Finally, 3H-thymidine incorporation in Hep G2 cells, in the presence of FCS or TGF alpha, was strongly inhibited by amiloride. In conclusion, in Hep G2 cells, pHi is mainly regulated by Na+/H+ exchange, which activity can be stimulated by EGF and TGF alpha, but not by IGF-II. Administration of TGF alpha stimulates DNA synthesis, an effect that is blocked by amiloride, an inhibitor of Na+/H+ exchanger. These data suggest that Na+/H+ exchange activation may play a critical role in the growth of some hepatic tumors.

摘要

细胞内pH值(pHi)在增殖刺激后静止细胞的代谢激活中起重要作用,并且在一些肝外肿瘤的生长过程中,钠氢交换活性是必需的。为了研究肝癌细胞内的酸碱平衡以及假定的肝脏生长因子对钠氢交换活性的影响,我们研究了Hep G2细胞(一种分化良好的肝癌细胞系)在静息状态下以及给予表皮生长因子(EGF)、转化生长因子-α(TGFα)和胰岛素样生长因子-II(IGF-II)后的细胞内pH值(pHi)调节情况。还研究了胎牛血清、TGFα和氨氯吡咪对3H-胸腺嘧啶核苷掺入的影响。氨氯吡咪(1 mmol/L)和去除细胞外钠会降低HEPES和KRB中的基础pHi。在HEPES中,细胞通过氨氯吡咪可抑制的钠氢交换从酸负荷(20 mmol/L NH4Cl)中恢复。在KRB中,一种额外的、DIDS可抑制的、依赖钠和碳酸氢根但不依赖氯离子的酸排出器(钠:碳酸氢根共转运体)被激活。未发现有作为酸加载器的氯/碳酸氢根交换的证据。给予EGF和TGFα,但不给予IGF-II,会导致基础pHi呈剂量依赖性、氨氯吡咪可抑制的升高,同时钠氢交换活性增加,使JH/pHi曲线向右移动。最后,在存在胎牛血清或TGFα的情况下,氨氯吡咪强烈抑制Hep G2细胞中3H-胸腺嘧啶核苷的掺入。总之,在Hep G2细胞中,pHi主要由钠氢交换调节,其活性可被EGF和TGFα刺激,但不能被IGF-II刺激。给予TGFα可刺激DNA合成,这种作用被钠氢交换抑制剂氨氯吡咪阻断。这些数据表明钠氢交换激活可能在某些肝癌的生长中起关键作用。

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