BLT1和BLT2:白三烯B4受体

Andrew M. Tager , Andrew D. Luster
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引用次数: 0

摘要

白三烯B4 (LTB4)的两个受体已被分子鉴定:BLT1和BLT2。这两种受体都是G蛋白偶联的7跨膜结构域受体,其基因在人和小鼠基因组中的位置非常接近。这两种受体对LTB4的亲和力和特异性不同:BLT1是LTB4特异性的高亲和力受体,而BLT2是一种低亲和力受体,也能结合其他二十烷类蛋白。这两种受体的表达模式也不同,BLT1主要在白细胞中表达,而BLT2则更普遍地表达。通过介导LTB4的活性,这些受体参与宿主免疫反应和炎症性疾病的发病机制。LTB4受体拮抗剂和BLT1靶向缺失小鼠在动物炎症模型中观察到的疾病严重程度降低,揭示了LTB4及其受体在调节病理性炎症中的重要作用。
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BLT1 and BLT2: the leukotriene B4 receptors
Two receptors for leukotriene B4 (LTB4) have been molecularly identified: BLT1 and BLT2. Both receptors are G protein-coupled seven transmembrane domain receptors, whose genes are located in very close proximity to each other in the human and mouse genomes. The two receptors differ in their affinity and specificity for LTB4: BLT1 is a high-affinity receptor specific for LTB4, whereas BLT2 is a low-affinity receptor that also binds other eicosanoids. The two receptors also differ in their pattern of expression with BLT1 being expressed primarily in leukocytes, whereas BLT2 is expressed more ubiquitously. By mediating the activities of LTB4, these receptors participate both in host immune responses and in the pathogenesis of inflammatory diseases. Reduced disease severity in animal inflammatory models seen with LTB4 receptor antagonists and in mice with targeted deletion of BLT1 have revealed important roles for LTB4 and its receptors in regulating pathologic inflammation.
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来源期刊
Prostaglandins, leukotrienes, and essential fatty acids
Prostaglandins, leukotrienes, and essential fatty acids Clinical Biochemistry, Endocrinology, Diabetes and Metabolism
CiteScore
5.30
自引率
0.00%
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0
审稿时长
64 days
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