Huang W W, Garcia-Zepeda E A, Sauty A, Oettgen H C, Rothenberg M E, Luster A D
Infectious Disease Unit, AIDS Research Center, Department of Medicine, Massachusetts General Hospital, Charlestown 02129, USA.
J Exp Med. 1998 Sep 21;188(6):1063-74. doi: 10.1084/jem.188.6.1063.
The movement of leukocytes into tissues is regulated by the local production of chemical mediators collectively referred to as chemoattractants. Although chemoattractants constitute a diverse array of molecules, including proteins, peptides, and lipids, they all appear to signal leukocytes through a related family of seven transmembrane-spanning G protein-coupled receptors. The eosinophil is a potent proinflammatory cell that is attracted into tissues during allergic inflammation, parasitic infection, and certain malignancies. Since the molecular mechanisms controlling eosinophil recruitment are incompletely understood, we performed a degenerate polymerase chain reaction on cDNA isolated from murine eosinophils to identify novel chemoattractant receptors. We report the isolation of a cDNA that encodes a 351-amino acid glycoprotein that is 78% identical to a human gene that has been reported to be a purinoceptor (P2Y7) and a leukotriene B4 (LTB4) receptor (BLTR). Chinese hamster ovary (CHO) cells transfected with this cDNA specifically bound [3H]LTB4 with a dissociation constant of 0.6 +/- 0.1 nM. Furthermore, LTB4 induced a dose-dependent intracellular calcium flux in transfected CHO cells. In contrast, [35S]dATP did not specifically bind to these transfectants. This mRNA was expressed at high levels in interleukin 5-exposed eosinophils, elicited peritoneal macrophages and neutrophils, and to a lesser extent interferon gamma stimulated macrophages. Low levels of expression were detected in the lung, lymph node, and spleen of unchallenged mice. Western blot analysis detected the mBLTR protein in murine eosinophils and alveolar macrophages as well as human eosinophils. In addition, elevated levels of mBLTR mRNA were found in the lungs of mice in a murine model of allergic pulmonary inflammation in a time course consistent with the influx of eosinophils. Our findings indicate that this murine receptor is an LTB4 receptor that is highly expressed on activated leukocytes, including eosinophils, and may play an important role in mediating eosinophil recruitment into inflammatory foci.
白细胞向组织中的迁移受统称为趋化因子的化学介质局部产生的调节。尽管趋化因子构成了各种各样的分子,包括蛋白质、肽和脂质,但它们似乎都通过一个相关的七跨膜G蛋白偶联受体家族向白细胞发出信号。嗜酸性粒细胞是一种强效的促炎细胞,在过敏性炎症、寄生虫感染和某些恶性肿瘤期间被吸引到组织中。由于控制嗜酸性粒细胞募集的分子机制尚未完全了解,我们对从小鼠嗜酸性粒细胞中分离的cDNA进行了简并聚合酶链反应,以鉴定新的趋化因子受体。我们报告分离出一种cDNA,它编码一种351个氨基酸的糖蛋白,与一个已报道的人基因有78%的同一性,该人基因被认为是嘌呤受体(P2Y7)和白三烯B4(LTB4)受体(BLTR)。用该cDNA转染的中国仓鼠卵巢(CHO)细胞以0.6±0.1 nM的解离常数特异性结合[3H]LTB4。此外,LTB4在转染的CHO细胞中诱导剂量依赖性的细胞内钙流。相比之下,[35S]dATP并不特异性结合这些转染细胞。这种mRNA在白细胞介素5刺激的嗜酸性粒细胞、诱发的腹腔巨噬细胞和中性粒细胞中高水平表达,在较小程度上在干扰素γ刺激的巨噬细胞中表达。在未受刺激的小鼠的肺、淋巴结和脾脏中检测到低水平的表达。蛋白质印迹分析在小鼠嗜酸性粒细胞、肺泡巨噬细胞以及人嗜酸性粒细胞中检测到mBLTR蛋白。此外,在过敏性肺炎小鼠模型的肺中发现mBLTR mRNA水平升高,其时间进程与嗜酸性粒细胞的流入一致。我们的研究结果表明,这种小鼠受体是一种LTB4受体,在包括嗜酸性粒细胞在内的活化白细胞上高度表达,可能在介导嗜酸性粒细胞募集到炎症灶中起重要作用。