Norrie D H, Wolstenholme J, Howcroft H, Stephen J
J Gen Virol. 1982 Sep;62 (Pt 1):127-36. doi: 10.1099/0022-1317-62-1-127.
A flame photometric technique is described for determining average values for intracellular [Na+] and [K+] in HeLa cells. Ion measurements were made on unwashed cells disrupted ultrasonically in the presence of residual medium; corrections for the latter were made by measurement of extracellular volume in cell plus medium preparations using 125I-labelled polyvinylpyrrolidone (PVP) as the marker in an isotopic dilution technique. Accurate measurement of the volume occupied by the cells was critical and required a concentration step. This was achieved by concentrating cell suspensions in a microhaematocrit centrifuge using calibrated capillary tubes. Most reliable values were obtained in our system using HeLa S3 (suspension) cells grown as monolayers, which were removed by EDTA and held in suspension for a minimum of 2 h. Uninfected HeLa cells had values of 20 to 30 and 110 to 120 mM for Na+ and K+ respectively. At 13 h after inoculation with vaccinia virus, a dramatic reversal in [Na+] and [K+] occurred, but throughout the infection cycle the total [Na+ + K+] varied little. The significance of these data is discussed in relation to theories of virus-induced modulation of protein synthesis in infected cells and in cell-free systems.
本文描述了一种火焰光度技术,用于测定HeLa细胞内[Na+]和[K+]的平均值。在残留培养基存在的情况下,对经超声破碎的未洗涤细胞进行离子测量;使用125I标记的聚乙烯吡咯烷酮(PVP)作为标记物,通过同位素稀释技术测量细胞加培养基制剂中的细胞外体积,对后者进行校正。准确测量细胞所占体积至关重要,且需要进行浓缩步骤。这是通过使用校准毛细管在微量血细胞比容离心机中浓缩细胞悬液来实现的。在我们的系统中,使用单层生长的HeLa S3(悬浮)细胞获得了最可靠的值,这些细胞用EDTA处理后悬浮至少2小时。未感染的HeLa细胞中Na+和K+的值分别为20至30 mM和110至120 mM。接种痘苗病毒后13小时,[Na+]和[K+]发生了显著逆转,但在整个感染周期中,[Na+ + K+]总量变化不大。结合病毒诱导感染细胞和无细胞系统中蛋白质合成调节的理论,对这些数据的意义进行了讨论。