Schneider C, Keeney D S, Boeglin W E, Brash A R
Department of Pharmacology, Vanderbilt University Medical School, Nashville, Tennessee 37232, USA.
Arch Biochem Biophys. 2001 Feb 15;386(2):268-74. doi: 10.1006/abbi.2000.2217.
Formation of the 12R-lipoxygenase product, 12R-hydroperoxyeicosatetraenoic acid (12R-HPETE), has been detected previously only in human skin (Boeglin et al. (1998) Proc. Natl. Acad. Sci. USA 95, 6744). The unexpected appearance of an EST sequence (AA649213) for human 12R-lipoxygenase from germinal center B lymphocytes purified from human tonsils prompted our search for the existence of the enzyme in this novel source. Incubation of [1-14C]arachidonic acid with homogenates of human tonsillar tissue yielded mixtures of radiolabeled 12-HETE and 15-HETE. Stereochemical analysis showed varying ratios of 12S- and 12R-HETE, while 15-HETE was exclusively of the S-configuration. Using stereospecifically labeled [10S-3H]- and [10R-3H]arachidonic acid substrates we detected pro-R hydrogen abstraction at carbon 10 associated with formation of 12R-HETE. This mechanistic evidence implicates a 12R-lipoxygenase in the biosynthesis of 12R-HETE. The mRNA for the enzyme was identified in tonsils by RT-PCR and Northern analysis. The cellular distribution was established by in situ hybridization. Unexpectedly, hybridization was not observed in the lymphocytes of the germinal centers. Specific reaction was restricted to squamous epithelial cells, including the epithelium lining the tonsillar crypts. In this location the 12R-lipoxygenase might help regulate differentiation of the epithelium or participate in lymphocyte- epithelial cell interactions.
此前仅在人体皮肤中检测到12R-脂氧合酶产物12R-氢过氧化二十碳四烯酸(12R-HPETE)(Boeglin等人,《美国国家科学院院刊》,1998年,第95卷,第6744页)。从人扁桃体中纯化的生发中心B淋巴细胞中意外出现了人12R-脂氧合酶的一个EST序列(AA649213),这促使我们探寻该酶在这一新来源中的存在情况。用[1-14C]花生四烯酸与人扁桃体组织匀浆一起孵育,产生了放射性标记的12-HETE和15-HETE混合物。立体化学分析显示12S-HETE和12R-HETE的比例各不相同,而15-HETE完全是S-构型。使用立体特异性标记的[10S-3H]-和[10R-3H]花生四烯酸底物,我们检测到与12R-HETE形成相关的碳10位上的前-R氢提取。这一机制证据表明12R-脂氧合酶参与了12R-HETE的生物合成。通过RT-PCR和Northern分析在扁桃体中鉴定出了该酶的mRNA。通过原位杂交确定了细胞分布。出乎意料的是,在生发中心的淋巴细胞中未观察到杂交。特异性反应仅限于鳞状上皮细胞,包括扁桃体隐窝内衬的上皮。在这个位置,12R-脂氧合酶可能有助于调节上皮细胞的分化或参与淋巴细胞与上皮细胞的相互作用。