Bautz F, Denzlinger C, Kanz L, Möhle R
Department of Medicine II, University of Tübingen, 72076 Tübingen, Germany.
Blood. 2001 Jun 1;97(11):3433-40. doi: 10.1182/blood.v97.11.3433.
Recent studies suggest that bone marrow (BM)-derived chemotactic mediators such as chemokines play key roles in hematopoietic stem cell trafficking. Lipid mediators, particularly leukotrienes, are involved in leukocyte chemotaxis during inflammation but have also been detected in the normal BM. Therefore, the effects of leukotrienes on hematopoietic progenitor cells were analyzed. Cysteinyl leukotrienes, particularly leukotriene D4 (LTD4), induced strong intracellular calcium fluxes and actin polymerization in mobilized and BM CD34(+) progenitors. Chemotaxis and in vitro transendothelial migration of CD34(+) and more primitive CD34(+)/CD38(-) cells were 2-fold increased by LTD4 at an optimum concentration of 25 to 50 nM. Accordingly, CD34(+) cells expressed the 7-transmembrane LTD4 receptor CysLT1 by reverse transcriptase-polymerase chain reaction and Western blot. Effects of LTD4 were suppressed by the CysLT1 receptor antagonist MK-571 and reduced by pertussis toxin. In contrast, LTB4 induced strong responses only in mature granulocytes. LTD4-induced calcium fluxes were also observed in granulocytes but were not reduced by MK-571, suggesting that these effects were mediated by other receptors (eg, CysLT2) rather than by CysLT1. In addition, expression of 5-lipoxygenase, the key enzyme of leukotriene biosynthesis, was detected in both hematopoietic progenitor cells and mature leukocytes. The study concludes that the functionally active LTD4 receptor CysLT1 is preferentially expressed in immature hematopoietic progenitor cells. LTD4 released in the BM might regulate progenitor cell trafficking and could also act as an autocrine mediator of hematopoiesis. This would be a first physiologic effect of cysteinyl leukotrienes apart from the many known pathophysiologic actions related to allergy and inflammation. (Blood. 2001;97:3433-3440)
近期研究表明,骨髓(BM)来源的趋化介质如趋化因子在造血干细胞归巢中起关键作用。脂质介质,尤其是白三烯,在炎症过程中参与白细胞趋化,但在正常骨髓中也有检测到。因此,分析了白三烯对造血祖细胞的影响。半胱氨酰白三烯,尤其是白三烯D4(LTD4),在动员的和骨髓CD34(+)祖细胞中诱导强烈的细胞内钙流和肌动蛋白聚合。在最佳浓度25至50 nM时,LTD4使CD34(+)和更原始的CD34(+)/CD38(-)细胞的趋化性和体外跨内皮迁移增加了2倍。相应地,通过逆转录酶-聚合酶链反应和蛋白质印迹法,CD34(+)细胞表达了7跨膜LTD4受体CysLT1。LTD4的作用被CysLT1受体拮抗剂MK-571抑制,并被百日咳毒素减弱。相反,LTB4仅在成熟粒细胞中诱导强烈反应。在粒细胞中也观察到LTD4诱导的钙流,但未被MK-571减弱,这表明这些作用是由其他受体(如CysLT2)而非CysLT1介导的。此外,在造血祖细胞和成熟白细胞中均检测到白三烯生物合成的关键酶5-脂氧合酶的表达。该研究得出结论,功能活跃的LTD4受体CysLT1优先在未成熟造血祖细胞中表达。骨髓中释放的LTD4可能调节祖细胞归巢,也可能作为造血的自分泌介质。这将是半胱氨酰白三烯除了与过敏和炎症相关许多已知病理生理作用之外的首个生理效应。(《血液》。2001年;97:3433 - 3440)