[Phospholipid-deacylating activities of the mouse peritoneal macrophages during phagocytosis].

G Matsuki, Y Kashiwabara, H Nakagawa
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引用次数: 1

Abstract

In the macrophages (M phi) obtained from mouse peritoneal exudates, five kinds of phospholipid-deacylating activities were detected using phosphatidylethanolamine (PE) and phosphatidylcholine (PC) labeled with [1-14C]oleic acid either in 1- or 2- position and 1- [1-14C]oleoyl-lysoPE, as substrates. Two types of phospholipipase A1 with pH optima of 4 to 6 and 8, respectively, and two types of phospholipase A2 activities with pH optima of 4 to 5 and 8, respectively, were identified. A detected lysophospholipase activity exhibited a broad pH optimum between 4 and 8. Both types of the phospholipase A1 and A2 of M phi hydrolyzed PE more than PC. Exogenously added Ca2+ did not increase the enzymatic activities. A comparison was made of three kinds of the M phi-phospholipid deacylating activities at pH8, after challenging the M phi with Mycobacterium lepraemurium, Escherichia coli, zymosan, or latex beads for 17 hours at 37 degrees C. The bacteria used to the phagocytosis were autoclaved. When the M phi were challenged with M. lepraemurium, the phospholipase A1, A2 and lysophospholipase activities were stimulated by about 160%, 150% and 140%, respectively. However, when challenged with E. coli, the phospholipase A1 activity remarkably decreased by about a third, although the phospholipase A2 activity was stimulated by about 150% that is similar to the challenge with M. lepraemurium. An inflammatory substance, zymosan seemed an effective inducer of the phospholipase A2, the enzymatic activity was remarkably stimulated by 260%, when challenged with 200 micrograms of zymosan. The increase in phospholipase A2 activity of the M phi pretreated with the bacteria or zymosan seems to result in an increase in the hydrolysis of arachidonic acid from the M phi-phospholipids to synthesize its inflammatory oxygenated metabolites. The lysophospholipase activity was not stimulated by the substances used to challenge the M phi, except for M. lepraemurium. No significant increase in three kinds of phospholipid-deacylating activities was observed after challenging the M phi with latex beads. It was considered from the above results that the M phi-phospholipid-deacylating activities at pH8 might be affected by sort of the ingested substances.

[小鼠腹腔巨噬细胞吞噬过程中磷脂-去乙酰化活性]。
以[1- 14c]油酸标记的1位或2位磷脂酰乙醇胺(PE)和磷脂酰胆碱(PC)和1- [1- 14c]油酰溶血酶为底物,对小鼠腹膜渗出液中巨噬细胞(M phi)的5种磷脂去酰活性进行了检测。鉴定出pH最优值分别为4 ~ 6和8的两种磷脂酶A1和pH最优值分别为4 ~ 5和8的两种磷脂酶A2。检测到的溶血磷脂酶活性在pH值4和8之间表现出广泛的最佳。两种类型的磷脂酶A1和A2都比PC更能水解PE。外源添加Ca2+不增加酶活性。用麻风分枝杆菌、大肠杆菌、酶酵素或乳胶珠在37℃下激噬M φ 17小时后,比较3种M φ在pH8下的磷脂去酰化活性。麻风分枝杆菌攻毒后,其磷脂酶A1、A2和溶血磷脂酶活性分别被刺激约160%、150%和140%。然而,当受到大肠杆菌的刺激时,磷脂酶A1的活性显著下降了约三分之一,尽管磷脂酶A2的活性被刺激了约150%,这与麻风分枝杆菌的刺激相似。酶多糖是一种炎性物质,似乎是一种有效的磷脂酶A2诱诱剂,当200微克酶多糖激发时,酶活性显著提高260%。经细菌或酵素预处理的m.phi磷脂酶A2活性的增加似乎导致m.phi磷脂水解花生四烯酸以合成其炎症氧合代谢物的增加。除麻风芽孢杆菌外,其他物质对溶血磷脂酶活性没有刺激作用。用乳胶珠刺激M φ后,3种磷脂去酰化活性均无显著升高。从上述结果可以看出,在pH8下,磷脂的脱羧活性可能受到摄入物质种类的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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