首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >ANNEXIN I CONCENTRATION, PHOSPHOLIPASE ACTIVITY AND THROMBOXANE SYNTHESIS IN IRRADIATED RAT LUNG
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ANNEXIN I CONCENTRATION, PHOSPHOLIPASE ACTIVITY AND THROMBOXANE SYNTHESIS IN IRRADIATED RAT LUNG

机译:辐照大鼠肺中Annexin I的浓度,磷脂酶活性和血栓烷的合成

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摘要

Annexin I, a member of a family of Ca2+-dependent phospholipid-binding proteins (PLBP), has been suggested as a regulator of prostaglandin metabolism as a result of its inhibitory effect on phospholipase A(2). 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 A(2) (TXA(2)) 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 TXA(2) by minced lung tissue was determined by radioimmunoassay of its stable metabolite TXB(2). Phospholipase activity was assayed by hydrolysis of [C-14]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 TXB(2)/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 A(2) 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. (C) 1995 by Radiation Research Society [References: 43]
机译:膜联蛋白I是Ca2 +依赖性磷脂结合蛋白(PLBP)家族的成员,由于其对磷脂酶A(2)的抑制作用,已被认为是前列腺素代谢的调节剂。在受辐照的组织中,前列腺素的合成增加,但尚未阐明引起这种增加的机理。可以想到,膜联蛋白I水平的降低导致磷脂酶活性的提高可能是前列腺素合成增强的原因。因此,我们测量了肺36 kDa PLBP的水平,它具有膜联蛋白I的特征,以及磷脂酶的活性和受辐射大鼠肺中血栓烷A(2)(TXA(2))的合成。用0、15或30 Gy的X射线照射大鼠的右肺,并在3个月后处死动物。通过将单层脂质体转移至多层脂质体的能力以及针对抗36 kDa兔PLBP抗血清的免疫印迹来分析磷脂结合蛋白。通过放射免疫法测定稳定的代谢产物TXB(2),确定了切碎的肺组织产生TXA(2)。通过水解[C-14]二油酰基磷脂酰胆碱测定磷脂酶活性。我们的结果表明,用30 Gy照射的肺的PLBP活性低于用0和15 Gy照射的肺的PLBP活性(8.82 +/- 0.47,而转移的9.73 +/- 0.49和9.95 +/- 0.78 nmol磷脂蛋白质)。蛋白质印迹表明,用30 Gy照射的肺中膜联蛋白I几乎完全耗尽。 30 Gy照射的肺中的磷脂酶活性也比0 Gy照射的肺中的磷脂酶活性低(0.23 +/- 0.01 vs 0.32 +/- 0.01 nmol释放的磷脂酰胆碱/ mg蛋白/ min,P <0.001)。不仅在肺匀浆的胞质或可溶性部分中观察到磷脂酶活性降低,而且在21,000g和100,000g离心后获得的沉淀物中均观察到磷脂酶活性降低。尽管磷脂酶活性有所下降,但用0和30辐照的肺部血栓烷的合成却增加了2.8倍(367 +/- 65,而1076 +/- 143 pg TXB(2)/ mg组织/ 10分钟相比) Gy)。这些结果与以下假设不一致:在受辐照的大鼠肺中血栓烷A(2)的合成增加是磷脂酶活性升高的直接结果。实际上,尽管假定的抑制剂Annexin I的浓度降低了,但受辐照的肺中磷脂酶的活性却降低了。 (C)1995年,由放射研究学会[参考:43]

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