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多形核白细胞对人血小板中花生四烯酸代谢的影响。

Influence of polymorphonuclear leukocytes on the metabolism of arachidonate in human platelets.

作者信息

Oudinet J P, Sraer J, Bens M, Ardaillou R

机构信息

I.N.S.E.R.M. Research Unit 64, Hôpital Tenon, Paris, France.

出版信息

Thromb Haemost. 1988 Aug 30;60(1):59-62.

PMID:3142092
Abstract

The effect of the association of purified polymorphonuclear leukocytes (PMNL) with platelets on arachidonic acid (AA) metabolism was studied in the presence of various concentrations of this fatty acid. Both thromboxane B2 (TXB2) and 12-hydroxy-eicosatetraenoic acid (12-HETE) were measured. In the presence of tracer doses of AA, addition of increasing amounts of PMNL to platelets inhibited in a concentration-dependent manner their 12-HETE and TXB2 production. This inhibition was not due to diversion of AA metabolism towards other pathways since, apart a negligible amount of 12,20-diHETE, no other product could be detected. Inhibition of platelet-TXB2 synthesis by PMNL persisted at increasing concentrations of AA below 16 microM. Above this concentration, TXB2 production by platelets incubated alone diminished progressively. Addition of PMNL blunted in part this inhibitory effect and even resulted, above 16 microM AA, in an increased production of TXB2. In contrast with what was observed for TXB2 formation, the inhibition of 12-HETE synthesis persisted when PMNL and platelets were coincubated in the presence of high doses of AA (163 microM). At this concentration, 15-HETE generation became apparent for each cell type incubated separately and was markedly enhanced in the coincubation studies. The present investigation demonstrates that the presence of PMNL modifies the metabolism of arachidonate by human platelets. Moreover, this cell-cell interaction markedly depends on the concentration of substrate. PMNL in excess may attenuate synthesis by platelets of their toxic products.

摘要

在不同浓度的花生四烯酸(AA)存在的情况下,研究了纯化的多形核白细胞(PMNL)与血小板结合对花生四烯酸代谢的影响。同时检测了血栓素B2(TXB2)和12-羟基-二十碳四烯酸(12-HETE)。在存在示踪剂量AA的情况下,向血小板中添加越来越多的PMNL会以浓度依赖的方式抑制它们的12-HETE和TXB2生成。这种抑制不是由于AA代谢转向其他途径,因为除了可忽略量的12,20-二HETE外,未检测到其他产物。在AA浓度低于16μM时,PMNL对血小板TXB2合成的抑制作用持续存在。高于此浓度时,单独孵育的血小板的TXB2生成逐渐减少。添加PMNL部分减弱了这种抑制作用,甚至在AA浓度高于16μM时导致TXB2生成增加。与TXB2形成的情况相反,当在高剂量AA(163μM)存在下将PMNL和血小板共同孵育时,对12-HETE合成的抑制作用持续存在。在此浓度下,单独孵育的每种细胞类型都明显产生15-HETE,并且在共同孵育研究中显著增强。本研究表明,PMNL的存在会改变人血小板中花生四烯酸的代谢。此外,这种细胞间相互作用明显取决于底物浓度。过量的PMNL可能会减弱血小板对其毒性产物的合成。

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