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Regulation of Immune Cell Migration by Sphingosine-1-Phosphate

机译:鞘氨醇-1-磷酸对免疫细胞迁移的调节

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摘要

Sphingosine-1-phosphate [S1P] is a potent bioactive sphingolipid molecule. In response to a stimulus, S1P is produced intracellularly by the action of two sphingosine kinases, and then it is exported to the extracellular environment or acts as an intracellular second messenger. S1P binds to its cognate G-protein coupled receptors, which are known as S1P receptors. There are five S1P receptors that have been identified in vertebrates. By activating S1P receptors, S1P controls a variety of physiological and pathological processes including cell migration, angiogenesis, vascular maturation, inflammation, and invasion, metastasis, and chemoresistance in cancer. S1P has emerged as a critical regulator of leukocyte migration and plays a central role in lymphocyte egress from the thymus and secondary lymphoid organs. In the current review article, we summarize the current understanding of the emigration of lymphocytes and other leukocytes from bone marrow, thymus and secondary lymphoid organs to the circulation, as well as the clinical implications of modulating the activity of the major S1P receptor, S1PR1.
机译:1-磷酸鞘氨醇[S1P]是一种有效的生物活性鞘脂分子。响应刺激,S1P在两个鞘氨醇激酶的作用下在细胞内产生,然后被输出到细胞外环境或充当细胞内第二信使。 S1P与其关联的G蛋白偶联受体结合,后者被称为S1P受体。在脊椎动物中已经鉴定出五种S1P受体。通过激活S1P受体,S1P可控制多种生理和病理过程,包括癌症中的细胞迁移,血管生成,血管成熟,炎症,侵袭,转移和化学耐药性。 S1P已成为白细胞迁移的关键调节剂,并在胸腺和继发性淋巴器官的淋巴细胞流出中发挥重要作用。在当前的综述文章中,我们总结了目前对淋巴细胞和其他白细胞从骨髓,胸腺和次要淋巴器官向循环系统迁移的了解,以及调节主要S1P受体S1PR1的活性的临床意义。

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