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水蛭Haementeria ghilianii大唾液腺细胞的细胞内pH值:调节及其对分泌的影响。

Intracellular pH of giant salivary gland cells of the leech Haementeria ghilianii: regulation and effects on secretion.

作者信息

Wuttke W A, Munsch T, Berry M S

机构信息

Biomedical and Physiological Research Group, School of Biological Sciences, University College of Swansea, Singleton Park, Wales, UK.

出版信息

J Exp Biol. 1994 Apr;189:179-98. doi: 10.1242/jeb.189.1.179.

Abstract
  1. Intracellular pH (pHi) and membrane potential (Em) of giant salivary gland cells of the leech, Haementeria ghilianii, were measured with double-barrelled, neutral-carrier, pH-sensitive microelectrodes. 2. Em was -51 +/- 11.2 mV and pHi was 6.98 +/- 0.1 (mean +/- S.D., N = 41) in Hepes-buffered saline (nominally HCO3(-)-free; extracellular pH, pHe = 7.4). pHi was independent of Em. 3. Amiloride (2 mmol l-1) had no effect on resting pHi or on pHi recovery from an acid load (induced by the NH4+ pre-pulse technique). Removal of external Na+ produced a progressive acidification which was blocked by amiloride, and the drug also slowed the recovery of pHi on reintroduction of Na+. The results indicate the presence of an electroneutral Na+/H+ exchanger whose access to amiloride is competitively blocked by Na+. 4. In certain smaller cells of the gland, which probably form a separate population, removal of external Na+ did not affect pHi, and recovery from an acid load was blocked by amiloride. There may, therefore, be two types of Na+/H+ exchanger, differing in reversibility and sensitivity to amiloride. 5. Recovery of pHi from NH4(+)-induced acid loading was not affected by bicarbonate-buffered saline (2% CO2; 11 mmol l-1 HCO3-) or by addition of the anion-exchange blocker SITS (10(-4) mol l-1). This suggests that there is no significant contribution of a HCO3(-)-dependent transport mechanism to pHi regulation in the gland cells. 6. Removal of external Cl- slowly reduced pHi and there was a transient increase (overshoot) in pHi when Cl- was reintroduced. These effects of Cl- are probably explained by changes in the Na+ gradient. Intracellular Na+ and Cl- activities were measured with ion-selective microelectrodes. 7. Acidification with NH4+ was difficult, probably because of the cells' poor permeability to this ion. Attempts to introduce NH4+ via the Na+ pump or Na+/Cl- transporter were not successful. The H+/K+ ionophore nigericin (1 microgram ml-1), however, produced a rapid and reversible acidification. 8. N-methylmaleimide (0.5-1 mmol l-1), which blocks proton-pumping ATPase, produced a prolonged acidification of almost 1 pH unit, well beyond the level expected for simple equilibration with pHe. The results are consistent with the presence of a vesicular proton pump, acidifying the secretory vesicles which pack the cell body. 9. NH4+ (50 mmol l-1) or trimethylamine (50 mmol l-1) increased pHi and stimulated salivary secretion, while propionate (50 mmol l-1) decreased pHi and stopped secretion.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 用双管中性载体pH敏感微电极测量了水蛭(Haementeria ghilianii)大唾液腺细胞的细胞内pH(pHi)和膜电位(Em)。2. 在赫佩斯缓冲盐溶液(名义上无HCO3(-);细胞外pH,pHe = 7.4)中,Em为-51±11.2 mV,pHi为6.98±0.1(平均值±标准差,N = 41)。pHi与Em无关。3. 氨氯地平(2 mmol l-1)对静息pHi或酸负荷(由NH4+预脉冲技术诱导)后的pHi恢复没有影响。去除细胞外Na+会导致逐渐酸化,氨氯地平可阻断这种酸化,并且该药物在重新引入Na+时也会减缓pHi的恢复。结果表明存在一种电中性的Na+/H+交换体,其对氨氯地平的亲和力被Na+竞争性阻断。4. 在腺体的某些较小细胞中,这些细胞可能构成一个单独的群体,去除细胞外Na+不会影响pHi,酸负荷后的恢复被氨氯地平阻断。因此,可能存在两种类型的Na+/H+交换体,在可逆性和对氨氯地平的敏感性方面有所不同。5. 用碳酸氢盐缓冲盐溶液(2% CO2;11 mmol l-1 HCO3-)或添加阴离子交换阻滞剂SITS(10(-4) mol l-1)对NH4(+)诱导的酸负荷后的pHi恢复没有影响。这表明HCO3(-)依赖性转运机制对腺体细胞中pHi调节没有显著贡献。6. 去除细胞外Cl-会缓慢降低pHi,当重新引入Cl-时,pHi会有短暂升高(过冲)。Cl-的这些作用可能是由Na+梯度的变化解释的。用离子选择性微电极测量了细胞内Na+和Cl-活性。7. 用NH4+酸化很困难,可能是因为细胞对该离子的通透性较差。试图通过Na+泵或Na+/Cl-转运体引入NH4+未成功。然而,H+/K+离子载体尼日利亚菌素(1微克/毫升)会产生快速且可逆的酸化。8. 阻断质子泵ATP酶的N-甲基马来酰亚胺(0.5 - 1 mmol l-1)会产生近1个pH单位的长时间酸化,远远超过与pHe简单平衡预期的水平。结果与存在囊泡质子泵一致,该质子泵使填充细胞体的分泌囊泡酸化。9. NH4+(50 mmol l-1)或三甲胺(5 mmol l-1)会升高pHi并刺激唾液分泌,而丙酸盐(50 mmol l-1)会降低pHi并停止分泌。(摘要截断于400字)

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