Shen Jianzhong, DiCorleto Paul E
Department of Cell Biology, Lerner Research Institute, Cleveland Clinic Lerner College of Medicine, Cleveland Clinic Foundation, 9500 Euclid Ave, Cleveland, OH 44195, USA.
Circ Res. 2008 Feb 29;102(4):448-56. doi: 10.1161/CIRCRESAHA.107.165795. Epub 2008 Jan 3.
Extensive research on the role of ADP in platelet activation led to the design of new anti-thrombotic drugs, such as clopidogrel (Plavix; sanofi-aventis); however, very little is known about the ADP-preferring nucleotide receptors (P2Y1, P2Y12, and P2Y13) in endothelium. Here, we show that ADP stimulates migration of cultured human umbilical vein endothelial cells (HUVECs) in both Boyden chamber and in vitro wound repair assays. This promigratory effect was mimicked by 2-MeSADP, but not by AMP, and was inhibited by MRS2179 (P2Y1 receptor antagonist) but not by AR-C69931MX (P2Y12/13 receptor antagonist). RT-PCR revealed abundant P2Y1, barely detectable P2Y12, and absent P2Y13 receptor message in these cells. In addition, both ADP and 2-MeSADP, but not AMP, activated the mitogen-activated protein kinase pathways as evidenced by increased phosphorylation of extracellular signal-regulated kinase (ERK)1/2, c-Jun N-terminal kinase (JNK), and p38 kinase. ADP also stimulated phosphorylation of p90RSK, a downstream substrate of phosphorylated ERK1/2, and induced phosphorylation of such transcription factors downstream of the JNK and p38 pathways as c-Jun and activating transcription factor-2. These signaling events were inhibited by MRS2179 but not by AR-C69931MX. Furthermore, blockade of the ERK or JNK pathways by U0126 and SP600125, respectively, abolished ADP- and 2-MeSADP-stimulated HUVEC migration. However, inhibition of the p38 pathway by SB203580 partially suppressed ADP- and 2-MeSADP-induced HUVEC migration. We conclude that ADP promotes human endothelial cell migration by activating P2Y1 receptor-mediated MAPK pathways, possibly contributing to reendothelialization and angiogenesis after vascular injury.
对二磷酸腺苷(ADP)在血小板激活中作用的广泛研究促使了新型抗血栓药物的设计,如氯吡格雷(波立维;赛诺菲 - 安万特公司);然而,关于内皮细胞中偏好ADP的核苷酸受体(P2Y1、P2Y12和P2Y13)却知之甚少。在此,我们表明,在博伊登小室实验和体外伤口修复实验中,ADP均可刺激培养的人脐静脉内皮细胞(HUVECs)迁移。2 - 甲基硫代二磷酸腺苷(2 - MeSADP)可模拟这种促迁移作用,但单磷酸腺苷(AMP)则不能,且该作用被MRS2179(P2Y1受体拮抗剂)抑制,但不被AR - C69931MX(P2Y12/13受体拮抗剂)抑制。逆转录 - 聚合酶链反应(RT - PCR)显示这些细胞中P2Y1受体信息丰富,P2Y12受体信息几乎检测不到,且不存在P2Y13受体信息。此外,ADP和2 - MeSADP均可激活丝裂原活化蛋白激酶途径,细胞外信号调节激酶(ERK)1/2、c - Jun氨基末端激酶(JNK)和p38激酶磷酸化增加即为证据,而AMP则不能。ADP还刺激了磷酸化ERK1/2的下游底物p90核糖体S6激酶(p90RSK)的磷酸化,并诱导了JNK和p38途径下游的转录因子如c - Jun和活化转录因子 - 2的磷酸化。这些信号转导事件被MRS2179抑制,但不被AR - C69931MX抑制。此外,分别用U0126和SP600125阻断ERK或JNK途径,可消除ADP和2 - MeSADP刺激的HUVEC迁移。然而,用SB203580抑制p38途径可部分抑制ADP和2 - MeSADP诱导的HUVEC迁移。我们得出结论,ADP通过激活P2Y1受体介导的丝裂原活化蛋白激酶途径促进人内皮细胞迁移,这可能有助于血管损伤后的再内皮化和血管生成。