Uchida Koji, Shibata Takahiro
Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, Japan.
Chem Res Toxicol. 2008 Jan;21(1):138-44. doi: 10.1021/tx700177j. Epub 2007 Dec 4.
Electrophilic molecules are endogenously generated and are causally involved in many pathophysiological effects. Prostaglandin D (20 (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)). 15d-PGJ (2) is an electrophile, which can covalently react via the Michael addition reaction with nucleophiles, such as the free sulfhydryls of glutathione and cysteine residues in cellular proteins that play an important role in the control of the redox cell-signaling pathways. Covalent binding of 15d-PGJ (2) to cellular proteins may be one of the mechanisms by which 15d-PGJ (2) induces a cellular response involved in most of the pathophysiological effects associated with inflammation. In the present perspective, we provide a comprehensive summary of 15d-PGJ (2) as an electrophilic mediator of cellular responses.
亲电分子是内源性产生的,并在许多病理生理效应中起因果作用。前列腺素D(20)(PGD(2))是多种组织中的主要环氧化酶产物,很容易脱水生成J(2)系列的环戊烯酮型前列腺素,如15-脱氧-Δ(12,14)-PGJ(2)(15d-PGJ(2))。15d-PGJ(2)是一种亲电试剂,它可以通过迈克尔加成反应与亲核试剂发生共价反应,例如谷胱甘肽的游离巯基和细胞蛋白中的半胱氨酸残基,这些在氧化还原细胞信号通路的控制中起重要作用。15d-PGJ(2)与细胞蛋白的共价结合可能是15d-PGJ(2)诱导参与大多数与炎症相关病理生理效应的细胞反应的机制之一。在本综述中,我们全面总结了15d-PGJ(2)作为细胞反应的亲电介质的情况。