Avery S V, Lloyd D, Harwood J L
School of Molecular and Medical Biosciences, School of Pure and Applied Biology, University of Wales College of Cardiff, U.K.
Biochem J. 1995 Dec 15;312 ( Pt 3)(Pt 3):811-6. doi: 10.1042/bj3120811.
The relationship between temperature-dependent changes in phagocytotic activity of Acanthamoeba castellanii and the fatty acid composition and physical properties of plasma membrane-enriched fractions were determined in cultures acclimated to 30 degrees C and 15 degrees C. Chilling (from 30 degrees C to 15 degrees C) had a very pronounced short-term inhibitory effect on phagocytosis only in stationary-phase cultures, which displayed a low degree of fatty acid unsaturation. A subsequent increase in phagocytosis by these cells was correlated with a low-temperature-induced increase in fatty acid unsaturation (shown previously [Jones, Lloyd and Harwood (1993) Biochem. J. 296, 183-188] to be due to n-6 desaturase induction). Plasma membrane-enriched fractions from 15 degrees C-acclimated cells also showed a marked increase in the relative proportion of polyunsaturated fatty acids. Steady-state fluorescence depolarization studies, using the membrane probe diphenylhexatriene, revealed increases in plasma membrane order with decreasing assay temperature. Over the upper assay-temperature range (25-40 degrees C), fluorescence anisotropy values were higher in membranes from 30 degrees C-acclimated cells; a 3.3 degrees C relative displacement of plots indicated that temperature-induced changes in membrane lipid composition compensated for approx. 22% of the ordering effect of low temperature. Changes in the temperature-dependence of fluorescence anisotropy, possibly corresponding to lateral phase separations or alterations in other bulk physical properties of membranes, occurred between 20 and 25 degrees C in membranes from 30 degrees C-acclimated cells and between 15 and 20 degrees C in membranes from 15 degrees C-acclimated cells. Fluorescence anisotropy plots were superimposed at assay temperatures between 5 and 15 degrees C. Short-term phagocytotic rates in whole cells decreased with assay temperature. Arrhenius discontinuities in rates of phagocytosis occurred at approx. 25.0 degrees C and 17.5 degrees C in 30 degrees C- and 15 degrees C-acclimated cells respectively, and in each case were thus within the temperature ranges of slope-change in the corresponding fluorescence anisotropy plots. The results show a direct correlation between plasma membrane fatty acid unsaturation, membrane physical properties and phagocytotic activity in A. castellanii. Therefore, a specific integrated physiological process has been correlated with fatty acid desaturase induction for the first time.
在适应30℃和15℃的培养物中,测定了卡氏棘阿米巴吞噬活性的温度依赖性变化与富含质膜组分的脂肪酸组成和物理性质之间的关系。低温处理(从30℃降至15℃)仅在脂肪酸不饱和度较低的稳定期培养物中对吞噬作用有非常明显的短期抑制作用。这些细胞随后吞噬作用的增加与低温诱导的脂肪酸不饱和度增加相关(先前已表明[琼斯、劳埃德和哈伍德(1993年)《生物化学杂志》296卷,183 - 188页]这是由于n - 6去饱和酶的诱导)。来自适应15℃细胞的富含质膜组分中多不饱和脂肪酸的相对比例也显著增加。使用膜探针二苯基己三烯进行的稳态荧光去极化研究表明,随着测定温度降低,质膜有序性增加。在较高的测定温度范围(25 - 40℃)内,来自适应30℃细胞的膜的荧光各向异性值更高;曲线相对位移3.3℃表明温度诱导的膜脂质组成变化补偿了约22%的低温有序化效应。来自适应30℃细胞的膜在20至25℃之间、来自适应15℃细胞的膜在15至20℃之间发生了荧光各向异性温度依赖性的变化,这可能对应于侧向相分离或膜其他整体物理性质的改变。在5至15℃的测定温度下,荧光各向异性曲线相互叠加。全细胞的短期吞噬速率随测定温度降低。在适应30℃和15℃的细胞中,吞噬作用速率的阿累尼乌斯不连续性分别出现在约25.0℃和17.5℃,并且在每种情况下都处于相应荧光各向异性曲线斜率变化的温度范围内。结果表明卡氏棘阿米巴的质膜脂肪酸不饱和度、膜物理性质和吞噬活性之间存在直接相关性。因此,首次将一个特定的综合生理过程与脂肪酸去饱和酶的诱导联系起来。