Boonstra J, Nelemans S A, Feijen A, Bierman A, Van Zoelen E J, Van der Saag P T, De Laat S W
Biochim Biophys Acta. 1982 Nov 22;692(3):321-9. doi: 10.1016/0005-2736(82)90380-7.
In this study the effects of experimental modifications of plasma membrane lipid lateral mobility on the electrical membrane properties and cation transport of mouse neuroblastoma cells, clone Neuro-2A, have been studied. Short-term supplementation of a chemically defined growth medium with oleic acid or linoleic acid resulted in an increase in the lateral mobility of lipids as inferred from fluorescence recovery after photobleaching of the lipid probe 3,3'-dioctadecylindocarbocyanide iodide. These changes were accompanied by a marked depolarization of the membrane potential from -51 mV to -36 mV, 1.5 h after addition, followed by a slow repolarization. Tracer flux studies, using 86Rb+ as a radioactive tracer for K+, demonstrated that the depolarization was not caused by changes in (Na+ + K+)-ATPase-mediated K+ influx or in the transmembrane K+ gradient. The permeability ratio (PNa/PK), determined from electrophysiological measurements, however, increased from 0.10 to 0.27 upon supplementation with oleic acid or linoleic acid. This transient rise of PNa/PK was shown by 24Na+ and 86Rb+ flux measurements to be due to both an increase of the Na+ permeability and a decrease of the K+ permeability. None of these effects occurred upon supplementation of the growth medium with stearic acid.
在本研究中,已对小鼠神经母细胞瘤细胞系Neuro - 2A的质膜脂质侧向流动性的实验性改变对其膜电特性和阳离子转运的影响进行了研究。用油酸或亚油酸对化学成分明确的生长培养基进行短期补充后,根据脂质探针3,3'-二辛基吲哚羰花青碘化物光漂白后的荧光恢复情况推断,脂质的侧向流动性增加。添加后1.5小时,这些变化伴随着膜电位从 -51 mV显著去极化至 -36 mV,随后缓慢复极化。使用⁸⁶Rb⁺作为K⁺的放射性示踪剂进行的示踪通量研究表明,去极化不是由(Na⁺ + K⁺)-ATP酶介导的K⁺内流或跨膜K⁺梯度的变化引起的。然而,根据电生理测量确定的通透率(PNa/PK)在添加油酸或亚油酸后从0.10增加到0.27。通过²⁴Na⁺和⁸⁶Rb⁺通量测量表明,PNa/PK的这种短暂升高是由于Na⁺通透性增加和K⁺通透性降低所致。在用硬脂酸补充生长培养基时,未出现这些效应中的任何一种。