Shibata Takahiro, Kondo Mitsuhiro, Osawa Toshihiko, Shibata Noriyuki, Kobayashi Makio, Uchida Koji
Laboratory of Food and Biodynamics, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, Japan.
J Biol Chem. 2002 Mar 22;277(12):10459-66. doi: 10.1074/jbc.M110314200. Epub 2002 Jan 10.
Prostaglandin D(2) (PGD(2)), a major cyclooxygenase product in a variety of tissues, readily undergoes dehydration to yield the cyclopentenone-type PGs of the J(2) series, such as 15-deoxy-Delta(12,14)-PGJ(2) (15d-PGJ(2)), which have been suggested to exert anti-inflammatory effects in vivo. Meanwhile, the mechanism of these effects is not well understood and the natural site and the extent of its production in vivo remain unclear. In the present study, we raised a monoclonal antibody specific to 15d-PGJ(2) and determined its production in inflammation-related events. The monoclonal antibody (mAb11G2) was raised against the 15d-PGJ(2)-keyhole limpet hemocyanin conjugate and was found to recognize free 15d-PGJ(2) specifically. The presence of 15d-PGJ(2) in vivo was immunohistochemically verified in the cytoplasm of most of the foamy macrophages in human atherosclerotic plaques. In addition, the immunostaining of lipopolysaccharide-stimulated RAW264.7 macrophages with mAb11G2 demonstrated an enhanced intracellular accumulation of 15d-PGJ(2), suggesting that the PGD(2) metabolic pathway, generating the anti-inflammatory PGs, is indeed utilized in the cells during inflammation. The activation of macrophages also resulted in the extracellular production of PGD(2), which was associated with a significant increase in the extracellular 15d-PGJ(2) levels, and the extracellular 15d-PGJ(2) production was reproduced by incubating PGD(2) in a cell-free medium and in phosphate-buffered saline. Moreover, using a chiral high performance liquid chromatography method for separation of PGD(2) metabolites, we established a novel metabolic pathway, in which PGD(2) is converted to 15d-PGJ(2) via an albumin-independent mechanism.
前列腺素D₂(PGD₂)是多种组织中主要的环氧化酶产物,很容易脱水生成J₂系列的环戊烯酮型前列腺素,如15-脱氧-Δ¹²,¹⁴-前列腺素J₂(15d-PGJ₂),有研究表明其在体内具有抗炎作用。同时,这些作用的机制尚未完全明确,其在体内的天然产生部位及产生程度仍不清楚。在本研究中,我们制备了一种针对15d-PGJ₂的单克隆抗体,并确定了其在炎症相关事件中的产生情况。该单克隆抗体(mAb11G2)是针对15d-PGJ₂-钥孔戚血蓝蛋白偶联物制备的,发现它能特异性识别游离的15d-PGJ₂。通过免疫组织化学方法在人动脉粥样硬化斑块中大多数泡沫巨噬细胞的细胞质中证实了15d-PGJ₂在体内的存在。此外,用mAb11G2对脂多糖刺激的RAW264.7巨噬细胞进行免疫染色,结果显示细胞内15d-PGJ₂的积累增加,这表明在炎症过程中细胞确实利用了产生抗炎性前列腺素的PGD₂代谢途径。巨噬细胞的激活还导致细胞外PGD₂的产生,这与细胞外15d-PGJ₂水平的显著增加有关,并且通过在无细胞培养基和磷酸盐缓冲盐溶液中孵育PGD₂可重现细胞外15d-PGJ₂的产生。此外,我们使用手性高效液相色谱法分离PGD₂代谢产物,建立了一种新的代谢途径,即PGD₂通过一种不依赖白蛋白的机制转化为15d-PGJ₂。