Ts'ao C, Tsao F H, Taylor J M, Ward W F, Molteni A
Department of Pathology, Northwestern University Medical School, Chicago, Illinois 60611.
Radiat Res. 1995 Apr;142(1):85-90.
Annexin I, a member of a family of Ca(2+)-dependent phospholipid-binding proteins (PLBP), has been suggested as a regulator of prostaglandin metabolism as a result of its inhibitory effect on phospholipase A2. Synthesis of prostaglandin is increased in irradiated tissue, but the mechanism underlying this increase has not been delineated. It is conceivable that a decrease in the level of annexin I resulting in increased phospholipase activity may be responsible for the enhanced synthesis of prostaglandin. Accordingly, we measured the level of a lung 36 kDa PLBP, which possesses characteristics of annexin I, as well as the activity of phospholipase and the synthesis of thromboxane A2 (TXA2) in irradiated rat lung. The right lung of rats was irradiated with 0, 15 or 30 Gy of X rays and the animals were sacrificed after 3 months. Phospholipid binding protein was assayed by its ability to transfer unilamellar liposomes to multilamellar liposomes and by immunoblotting against anti-36 kDa rabbit PLBP antisera. Production of TXA2 by minced lung tissue was determined by radioimmunoassay of its stable metabolite TXB2. Phospholipase activity was assayed by hydrolysis of [14C]dioleoylphosphatidylcholine. Our results showed that PLBP activity in the lungs irradiated with 30 Gy was lower than that in the lungs irradiated with 0 and 15 Gy (8.82 +/- 0.47 compared to 9.73 +/- 0.49 and 9.95 +/- 0.78 nmol phospholipid transferred/mg protein, respectively). Western blotting demonstrated a near total depletion of annexin I in the lungs irradiated with 30 Gy. Phospholipase activity was also lower in the lungs irradiated with 30 Gy compared to that in the lungs irradiated with 0 Gy (0.23 +/- 0.01 vs 0.32 +/- 0.01 nmol phosphatidylcholine liberated/mg protein/min, P < 0.001). Reduced phospholipase activity was observed not only in the cytosolic or soluble fraction of lung homogenate, but also in precipitates obtained after 21,000g and 100,000g centrifugation. Despite this decline in phospholipase activity, there was a 2.8-fold increase in the synthesis of thromboxane (367 +/- 65 compared to 1076 +/- 143 pg TXB2/mg tissue/10 min for lungs irradiated with 0 and 30 Gy, respectively). These results are not consistent with the hypothesis that increased synthesis of thromboxane A2 in irradiated rat lung is a direct result of elevated phospholipase activity. In fact, phospholipase activity is decreased in the irradiated lung, despite a decline in the concentration of annexin I, its putative inhibitor.
膜联蛋白I是一种依赖钙离子的磷脂结合蛋白(PLBP)家族成员,由于其对磷脂酶A2具有抑制作用,已被认为是前列腺素代谢的调节剂。辐射组织中前列腺素的合成增加,但其增加的潜在机制尚未阐明。可以想象,膜联蛋白I水平的降低导致磷脂酶活性增加,可能是前列腺素合成增强的原因。因此,我们测量了一种具有膜联蛋白I特征的肺36 kDa PLBP的水平,以及辐射大鼠肺中磷脂酶的活性和血栓素A2(TXA2)的合成。给大鼠的右肺照射0、15或30 Gy的X射线,3个月后处死动物。通过其将单层脂质体转移到多层脂质体的能力以及针对抗36 kDa兔PLBP抗血清的免疫印迹法来检测磷脂结合蛋白。通过对其稳定代谢物TXB2的放射免疫测定来确定切碎的肺组织中TXA2的产生。通过[14C]二油酰磷脂酰胆碱的水解来检测磷脂酶活性。我们的结果表明,照射30 Gy的肺中的PLBP活性低于照射0和15 Gy的肺(分别为8.82±0.47,而照射0和15 Gy的肺分别为9.73±0.49和9.95±0.78 nmol磷脂转移/mg蛋白质)。蛋白质印迹法显示,照射30 Gy的肺中膜联蛋白I几乎完全耗尽。与照射0 Gy的肺相比,照射30 Gy的肺中磷脂酶活性也较低(0.23±0.01对0.32±0.01 nmol磷脂酰胆碱释放/mg蛋白质/分钟,P<0.001)。不仅在肺匀浆的胞质或可溶部分观察到磷脂酶活性降低,在21,000g和100,000g离心后获得的沉淀物中也观察到降低。尽管磷脂酶活性下降,但血栓素的合成增加了2.8倍(照射0和30 Gy的肺分别为1076±143与367±65 pg TXB2/mg组织/10分钟)。这些结果与辐射大鼠肺中血栓素A2合成增加是磷脂酶活性升高的直接结果这一假设不一致。事实上,尽管其假定的抑制剂膜联蛋白I的浓度下降,但照射肺中的磷脂酶活性仍降低。