Suppr超能文献

激动剂诱导的前列腺素E1与前列腺素E2生成的调控:一项质谱分析

Regulation of agonist-induced prostaglandin E1 versus prostaglandin E2 production. A mass analysis.

作者信息

Rubin D, Laposata M

机构信息

Department of Pathology, Massachusetts General Hospital, Boston.

出版信息

J Biol Chem. 1991 Dec 15;266(35):23618-23.

PMID:1748640
Abstract

Prostaglandin E1 (PGE1) and prostaglandin E2 (PGE2), derived by enzymatic oxidation of cellular dihomogammalinolenic acid (DHLA) and arachidonic acid (AA), respectively, have diverse and, at times, distinct biological actions. It has been suggested that PGE1 specifically inhibits a variety of inflammatory processes, and, in light of the potential therapeutic benefit of PGE1 and its fatty acid precursor in inflammatory disorders, there is growing interest in the biochemical mechanisms which determine the balance between PGE1 and PGE2 synthesis. Metabolic studies in this area have been hampered by the difficulties in measuring the extremely small masses of these prostaglandins which are generated in cell culture systems. We studied the regulation of PGE1 versus PGE2 synthesis using an essential fatty acid-deficient, PGE-producing, mouse fibrosarcoma cell line, EFD-1. Because EFD-1 cells contain no endogenous AA or DHLA, we were able to replete the cells with AA and DHLA of known specific activities; thus, the mass of both cellular AA and DHLA, and synthesized PGE1 and PGE2, could be accurately determined. The major finding of this study is that production of PGE2 was highly favored over production of PGE1 due to preferential incorporation of AA versus DHLA into, and release from, the total cellular phospholipid pool. Further, we correlated the selective release of AA versus DHLA from total cellular phospholipids with the selective incorporation of AA versus DHLA into specific phospholipid pools. In addition, we showed that conversion of DHLA to AA by delta 5 desaturase was enhanced by increasing the cellular mass of n-6 fatty acids and by increasing the cell proliferative activity. Together, these results indicate that the relative abundance of PGE2 versus PGE1 in vivo is not merely a function of the relative abundance of AA versus DHLA in tissues, but also relates to markedly different cellular metabolism of these two fatty acids.

摘要

前列腺素E1(PGE1)和前列腺素E2(PGE2)分别由细胞双高γ-亚麻酸(DHLA)和花生四烯酸(AA)经酶促氧化产生,它们具有多种、有时甚至是截然不同的生物学作用。有人提出PGE1能特异性抑制多种炎症过程,鉴于PGE1及其脂肪酸前体在炎症性疾病中的潜在治疗益处,人们对决定PGE1和PGE2合成平衡的生化机制越来越感兴趣。该领域的代谢研究因难以测量细胞培养系统中产生的极少量这些前列腺素而受阻。我们使用一种必需脂肪酸缺乏、产生PGE的小鼠纤维肉瘤细胞系EFD-1研究了PGE1与PGE2合成的调节。由于EFD-1细胞不含内源性AA或DHLA,我们能够用已知比活性的AA和DHLA使细胞重新充满;因此,可以准确测定细胞内AA和DHLA以及合成的PGE1和PGE2的量。本研究的主要发现是,由于AA与DHLA优先掺入总细胞磷脂池并从其中释放,PGE2的产生比PGE1的产生更受青睐。此外,我们将AA与DHLA从总细胞磷脂中的选择性释放与AA与DHLA选择性掺入特定磷脂池相关联。另外,我们表明,通过增加n-6脂肪酸的细胞量和增加细胞增殖活性,δ5去饱和酶将DHLA转化为AA的过程得到增强。总之,这些结果表明,体内PGE2与PGE1的相对丰度不仅是组织中AA与DHLA相对丰度的函数,还与这两种脂肪酸明显不同的细胞代谢有关。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验