Aarstad H J, Kolset S O, Seljelid R
Institute of Medical Biology, University of Tromsø, Norway.
Scand J Immunol. 1991 Jun;33(6):673-81. doi: 10.1111/j.1365-3083.1991.tb02540.x.
Macrophages were harvested from home cage control (HCC) mice, and from mice which had been stressed by repeated brief exposures (3-8 min) to cold water at 10-15 degrees C twice daily for 8 or 14 days. Macrophages obtained from mice stressed 8 or 14 days compared to macrophages from HCC mice showed in vitro increased amounts of membrane-bound prothrombinase activity, whereas the thrombin degradation activity was unchanged. Furthermore, macrophages of mice stressed 8 days showed increased release of coagulation factor X/Xa to supernatant in vitro. These findings suggest an increased amount of prothrombinase complex enzymes on the surface of macrophages from mice stressed 8 days, and increased activity of the prothrombinase enzyme in macrophages from mice stressed 14 days. The synthesis of proteoglycans (PG) and glycosaminoglycans (GAG) was increased in macrophages from mice stressed 8 days compared to macrophages from HCC mice and mice stressed 14 days. When macrophages from mice stressed 8 days or HCC mice were stimulated in vitro with phorbol myristate acetate (PMA) and IL-1 or PMA and IL-2, a changed PG/GAG synthesis was observed only in macrophages from the HCC animals. Furthermore, both the tumour cytotoxicity and the released tumour necrosis factor (TNF) were decreased from macrophages from mice stressed 14 days compared to HCC mice. The results suggest that the macrophages of stressed mice have an altered mode of function more complex than a simple general suppression or activation.
巨噬细胞取自笼养对照(HCC)小鼠,以及每天两次在10 - 15摄氏度的冷水中反复短暂暴露(3 - 8分钟),持续8天或14天的应激小鼠。与HCC小鼠的巨噬细胞相比,取自应激8天或14天小鼠的巨噬细胞在体外显示膜结合凝血酶原酶活性增加,而凝血酶降解活性未改变。此外,应激8天小鼠的巨噬细胞在体外向上清液中释放的凝血因子X/Xa增加。这些发现表明,应激8天小鼠的巨噬细胞表面凝血酶原酶复合酶数量增加,应激14天小鼠的巨噬细胞中凝血酶原酶活性增加。与HCC小鼠和应激14天小鼠的巨噬细胞相比,应激8天小鼠的巨噬细胞中蛋白聚糖(PG)和糖胺聚糖(GAG)的合成增加。当用佛波酯肉豆蔻酸酯乙酸盐(PMA)和IL - 1或PMA和IL - 2体外刺激应激8天小鼠或HCC小鼠的巨噬细胞时,仅在HCC动物的巨噬细胞中观察到PG/GAG合成的变化。此外,与HCC小鼠相比,应激14天小鼠的巨噬细胞的肿瘤细胞毒性和释放的肿瘤坏死因子(TNF)均降低。结果表明,应激小鼠的巨噬细胞具有比简单的一般抑制或激活更复杂的功能改变模式。