Rossmann H, Bachmann O, Vieillard-Baron D, Gregor M, Seidler U
First Department of Medicine, Eberhard-Karls Universität, Tübingen, Germany.
Gastroenterology. 1999 Jun;116(6):1389-98. doi: 10.1016/s0016-5085(99)70503-2.
BACKGROUND & AIMS: The gastric epithelium protects itself against luminal acid by secreting HCO3--rich fluid into the mucous layer and by HCO3--dependent intracellular pH regulation, but the basolateral HCO3- uptake mechanisms are incompletely characterized. This study examined the expression and functional significance of the Na+/HCO3- cotransporters NBC1 and NBC2 in rabbit gastric epithelial cells.
Rabbit NBC1 and NBC2 complementary DNA fragments were cloned and sequenced, and cellular expression levels were assessed by semiquantitative polymerase chain reaction. Na+/HCO3- cotransport activity was measured fluorometrically in cultured rabbit parietal and mucous cells.
NBC1 expression was 4.5-fold lower in the stomach than kidney cortex and 5.5-fold higher in mucous than parietal cells. NBC2 expression in the stomach was much lower than in the eye, approximately 4-fold lower than NBC1 expression in the stomach, and 2.5-fold higher in mucous than parietal cells. The Na+- and HCO3--dependent, dimethylamiloride-insensitive (which at 500 micromol/L completely inhibits all Na+/H+ exchanger isoforms) base influx rates were 4.6 +/- 0.02 and 16.2 +/- 0.04 mmol/L/min in acidified parietal and mucous cells, respectively, and were not significantly different in the absence of Cl-.
This study shows that NBC1 and NBC2 are expressed in rabbit stomach, with high levels in mucous cells where Na+/HCO3- cotransport is the major base-importing mechanism in the presence of CO2/HCO3-.
胃上皮细胞通过向黏液层分泌富含HCO3-的液体以及依赖HCO3-的细胞内pH调节来保护自身免受管腔酸的侵害,但基底外侧HCO3-摄取机制尚未完全明确。本研究检测了兔胃上皮细胞中Na+/HCO3-共转运体NBC1和NBC2的表达及其功能意义。
克隆并测序兔NBC1和NBC2互补DNA片段,通过半定量聚合酶链反应评估细胞表达水平。用荧光法测量培养的兔壁细胞和黏液细胞中的Na+/HCO3-共转运活性。
胃中NBC1的表达比肾皮质低4.5倍,在黏液细胞中比壁细胞高5.5倍。胃中NBC2的表达远低于眼中的表达,比胃中NBC1的表达低约4倍,在黏液细胞中比壁细胞高2.5倍。在酸化的壁细胞和黏液细胞中,Na+和HCO3-依赖性、对二甲基amiloride不敏感(500 μmol/L时可完全抑制所有Na+/H+交换异构体)的碱流入速率分别为4.6±0.02和16.2±0.04 mmol/L/分钟,在无Cl-时无显著差异。
本研究表明,NBC1和NBC2在兔胃中表达,在黏液细胞中水平较高,在有CO2/HCO3-存在时,Na+/HCO3-共转运是主要的碱导入机制。