Membrane potentials, electrolyte contents, cell pH, and some enzyme activities of fibroblasts.

In Vitro Pub Date : 1984-09-01 DOI:10.1007/BF02618872
Y C Yen-Chow, S Y Chow, W S Jee, D M Woodbury
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引用次数: 5

Abstract

The resting membrane potential of the cultured fibroblasts derived from rabbit subcutaneous tissues was -10.2 +/- 0.20 mV (n = 390). This potential was affected by the potassium concentration in the culture medium, but not by other chemical or hormonal preparations, such as dibutyryladenosine 3',5'-cyclic monophosphate (0.5 to 5.0 mmol/l), sodium fluoride (10(-5) to 10(-4) M), hydrocortisone (10(-7) to 10(-6) M), parathyroid extract (0.5 to 1.0 U/ml), or thyrotrophin (5 to 10 mU/ml). The Na+, K+, and Cl- concentrations of the cultured fibroblasts were 35.4, 85.7, and 22.6 mmol/l cell water, respectively. The water and protein contents of these cells were 82.1 and 9.18 g/100-g cells, respectively. The intracellular pH of fibroblasts as determined by [14C] dimethyloxazolidine-2, 4-dione, and 3H2O ranged between 6.9 and 7.1 when the pH of the culture medium was maintained at 7.4. The activities of Na+, K+-, HCO3(-)-, and Ca++, Mg++-ATPases in these cultured cells were 19.0 +/- 2.1, 13.6 +/- 2.1, and 6.6 +/- 1.2 nmol pi/mg protein per minute, respectively, and the carbonic anhydrase activity was 0.054 U/mg protein. Calculations based on the values for the membrane potential and the electrolyte concentrations observed in this study indicate that Na+, K+, Cl-, and H+ are not distributed according to their electrochemical gradients across the cell membrane. Na+, Cl-, and H+ are actively transported out of the cells and K+ into the cells.

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膜电位、电解质含量、细胞pH和成纤维细胞的一些酶活性。
兔皮下组织成纤维细胞静息膜电位为-10.2 +/- 0.20 mV (n = 390)。这种电位受培养基中钾浓度的影响,但不受其他化学制剂或激素制剂的影响,如3',5'-环单磷酸二丁基腺苷(0.5至5.0 mmol/l),氟化钠(10(-5)至10(-4)M),氢化可的松(10(-7)至10(-6)M),甲状旁腺提取物(0.5至1.0 U/ml)或促甲状腺激素(5至10 mU/ml)。Na+、K+和Cl-浓度分别为35.4、85.7和22.6 mmol/l细胞水。细胞含水量为82.1 g/100 g,蛋白质含量为9.18 g/100 g。当培养基pH保持在7.4时,用[14C]二甲基氯恶唑烷- 2,4 -二酮和3H2O测定成纤维细胞内pH值在6.9 ~ 7.1之间。Na+、K+-、HCO3(-)-和Ca++、Mg++- atp酶的活性分别为19.0 +/- 2.1、13.6 +/- 2.1和6.6 +/- 1.2 nmol pi/ Mg蛋白/ min,碳酸酐酶活性为0.054 U/ Mg蛋白/ min。根据本研究中观察到的膜电位值和电解质浓度的计算表明,Na+、K+、Cl-和H+并不是按照它们在细胞膜上的电化学梯度分布的。Na+、Cl-和H+被主动地运出细胞,K+被主动地运入细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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