Bell C L, Quinton P M
Division of Biomedical Sciences, University of California, Riverside 92521.
In Vitro Cell Dev Biol. 1991 Jan;27(1):47-54. doi: 10.1007/BF02630894.
Primary cultures of human reabsorptive sweat duct cells were grown in MCDB 170 medium buffered with either HEPES, bicarbonate, or a mixture of HEPES and bicarbonate buffers. Cultures grown in MCDB media containing bicarbonate seemed to differentiate into a multilayered, keratinized epithelium and began senescing after 1 wk in culture. In contrast, cultures grown in media containing HEPES as the only buffer seemed to undergo a selection process, resulting in the outgrowth of cells that did not multilayer or keratinize extensively for up to 3 or 4 wk in culture. Despite marked differences in growth, cells grown in both bicarbonate and HEPES-buffered media retained electrophysiologic characteristics appropriate to the progenitor. Mean resting potentials were -21.8 +/- 0.8 mV (n = 82), -23.3 +/- 1.3 mV (n = 70) and -18.2 +/- 0.8 mV (n = 82) for duct cells grown in HEPES, bicarbonate, and HEPES-bicarbonate media, respectively. Substitution of Cl- with the impermeant anion gluconate in the bathing medium caused membrane potential depolarization in all media, revealing the presence of a Cl- conductance. Administration of the Na+ conductance inhibitor amiloride hyperpolarized the mean resting potential of cells grown in HEPES medium (-6.8 +/- 0.6 mV, n = 68), bicarbonate medium (-6.9 +/- 0.5 mV, n = 60), and HEPES-bicarbonate medium (-5.9 +/- 0.6 mV, n = 69), demonstrating expression of a Na+ conductance. We observed some but minimal variation with age in any of these conditions.
人重吸收性汗腺导管细胞的原代培养物在含有HEPES、碳酸氢盐或HEPES与碳酸氢盐缓冲液混合物缓冲的MCDB 170培养基中生长。在含有碳酸氢盐的MCDB培养基中生长的培养物似乎分化为多层角质化上皮,并在培养1周后开始衰老。相比之下,在仅含有HEPES作为缓冲液的培养基中生长的培养物似乎经历了一个选择过程,导致在培养长达3或4周时,未广泛形成多层或角质化的细胞生长。尽管生长存在显著差异,但在碳酸氢盐和HEPES缓冲培养基中生长的细胞都保留了适合祖细胞的电生理特性。对于在HEPES、碳酸氢盐和HEPES - 碳酸氢盐培养基中生长的导管细胞,平均静息电位分别为-21.8±0.8 mV(n = 82)、-23.3±1.3 mV(n = 70)和-18.2±0.8 mV(n = 82)。在浴液培养基中用不透性阴离子葡萄糖酸盐替代Cl-会导致所有培养基中的膜电位去极化,表明存在Cl-电导。给予Na+电导抑制剂氨氯吡咪会使在HEPES培养基(-6.8±0.6 mV,n = 68)、碳酸氢盐培养基(-6.9±0.5 mV,n = 60)和HEPES - 碳酸氢盐培养基(-5.9±0.6 mV,n = 69)中生长的细胞的平均静息电位超极化,证明表达了Na+电导。在任何这些条件下,我们观察到随着年龄的增长有一些但极小的变化。