Kanda Hidenobu, Newton Rebecca, Klein Russell, Morita Yuka, Gunn Michael D, Rosen Steven D
Department of Anatomy, Program in Immunology, Cardiovascular Research Institute, University of California San Francisco, San Francisco, California 94143, USA.
Nat Immunol. 2008 Apr;9(4):415-23. doi: 10.1038/ni1573. Epub 2008 Mar 9.
The extracellular lysophospholipase D autotaxin (ATX) and its product, lysophosphatidic acid, have diverse functions in development and cancer, but little is known about their functions in the immune system. Here we found that ATX had high expression in the high endothelial venules of lymphoid organs and was secreted. Chemokine-activated lymphocytes expressed receptors with enhanced affinity for ATX, which provides a mechanism for targeting the secreted ATX to lymphocytes undergoing recruitment. Lysophosphatidic acid induced chemokinesis in T cells. Intravenous injection of enzymatically inactive ATX attenuated the homing of T cells to lymphoid tissues, probably through competition with endogenous ATX and exertion of a dominant negative effect. Our results support the idea of a new and general step in the homing cascade in which the ectoenzyme ATX facilitates the entry of lymphocytes into lymphoid organs.
细胞外溶血磷脂酶D自分泌运动因子(ATX)及其产物溶血磷脂酸在发育和癌症中具有多种功能,但它们在免疫系统中的功能却鲜为人知。在这里,我们发现ATX在淋巴器官的高内皮微静脉中高表达并分泌。趋化因子激活的淋巴细胞表达对ATX具有增强亲和力的受体,这为将分泌的ATX靶向正在招募的淋巴细胞提供了一种机制。溶血磷脂酸诱导T细胞趋化运动。静脉注射无酶活性的ATX可减弱T细胞向淋巴组织的归巢,这可能是通过与内源性ATX竞争并发挥显性负效应实现的。我们的结果支持了归巢级联反应中一个新的普遍步骤的观点,即胞外酶ATX促进淋巴细胞进入淋巴器官。