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1
Complement receptor enhancement and chemotaxis of human neutrophils and eosinophils by leukotrienes and other lipoxygenase products.白三烯及其他脂氧合酶产物对人中性粒细胞和嗜酸性粒细胞补体受体的增强作用及趋化作用。
Clin Exp Immunol. 1982 Mar;47(3):541-7.
2
Mediation of leukocyte components of inflammatory reactions by lipoxygenase products of arachidonic acid.花生四烯酸的脂氧合酶产物对炎症反应中白细胞成分的介导作用。
Adv Prostaglandin Thromboxane Leukot Res. 1982;9:273-82.
3
Enhancement of neutrophil- and eosinophil-mediated complement-dependent killing of schistosomula of Schistosoma mansoni in vitro by leukotriene B4.白三烯B4在体外增强嗜中性粒细胞和嗜酸性粒细胞介导的曼氏血吸虫童虫补体依赖性杀伤作用。
Clin Exp Immunol. 1983 Jun;52(3):519-27.
4
Metabolism of arachidonic acid through the 5-lipoxygenase pathway in normal human peritoneal macrophages.正常人腹膜巨噬细胞中花生四烯酸通过5-脂氧合酶途径的代谢
J Immunol. 1988 Sep 15;141(6):2104-9.
5
Modulation of human neutrophil function by monohydroxy-eicosatetraenoic acids.单羟基二十碳四烯酸对人中性粒细胞功能的调节
Immunology. 1980 Apr;39(4):491-501.
6
Lipoxygenase pathways of macrophages.巨噬细胞的脂氧合酶途径
Fed Proc. 1985 Nov;44(14):2933-6.
7
Effects of exogenous arachidonic, eicosapentaenoic, and docosahexaenoic acids on the generation of 5-lipoxygenase pathway products by ionophore-activated human neutrophils.外源性花生四烯酸、二十碳五烯酸和二十二碳六烯酸对离子载体激活的人中性粒细胞生成5-脂氧合酶途径产物的影响。
J Clin Invest. 1984 Dec;74(6):1922-33. doi: 10.1172/JCI111612.
8
An analysis of the relationship between 5-lipoxygenase product generation and the secretion of preformed mediators from mouse bone marrow-derived mast cells.小鼠骨髓来源肥大细胞中5-脂氧合酶产物生成与预先形成的介质分泌之间关系的分析
J Immunol. 1984 Aug;133(2):938-45.
9
Stereospecificity of leukotriene B4 and structure-function relationships for chemotaxis of human neutrophils.白三烯B4的立体特异性与人中性粒细胞趋化性的结构-功能关系
J Immunol. 1984 Sep;133(3):1477-82.
10
Comparison of 5- and 15-lipoxygenase activities in blood and alveolar leukocyte preparations from normal subjects and patients with eosinophilia.正常受试者和嗜酸性粒细胞增多症患者血液及肺泡白细胞制剂中5-脂氧合酶和15-脂氧合酶活性的比较。
Prostaglandins Leukot Med. 1986 Aug;23(2-3):191-9. doi: 10.1016/0262-1746(86)90185-x.

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Development of Adaptive Immunity and Its Role in Lung Remodeling.适应性免疫的发展及其在肺重塑中的作用。
Adv Exp Med Biol. 2023;1426:287-351. doi: 10.1007/978-3-031-32259-4_14.
2
Leukotriene D induces chemotaxis in human eosinophilc cell line, EoL-1 cells via CysLT1 receptor activation.白三烯D通过激活半胱氨酰白三烯1受体,诱导人嗜酸性粒细胞系EoL-1细胞发生趋化作用。
Heliyon. 2017 Dec 1;3(11):e00464. doi: 10.1016/j.heliyon.2017.e00464. eCollection 2017 Nov.
3
[Not Available].[无可用内容]
Doc Ophthalmol. 1984 May;57(3):215-262. doi: 10.1007/BF00143085.
4
Cooperative role of endogenous leucotrienes and platelet-activating factor in ischaemia-reperfusion-mediated tissue injury.内源性白三烯和血小板激活因子在缺血再灌注介导的组织损伤中的协同作用。
J Cell Mol Med. 2013 Dec;17(12):1554-65. doi: 10.1111/jcmm.12118. Epub 2013 Nov 1.
5
Disruption of the 5-lipoxygenase pathway attenuates atherogenesis consequent to COX-2 deletion in mice.5-脂氧合酶途径的破坏可减轻 COX-2 缺失所致的小鼠动脉粥样硬化形成。
Proc Natl Acad Sci U S A. 2012 Apr 24;109(17):6727-32. doi: 10.1073/pnas.1115313109. Epub 2012 Apr 9.
6
Leukotrienes are involved in leukocyte recruitment induced by live Histoplasma capsulatum or by the beta-glucan present in their cell wall.白三烯参与由活荚膜组织胞浆菌或其细胞壁中存在的β-葡聚糖诱导的白细胞募集过程。
Br J Pharmacol. 1999 Dec;128(7):1529-37. doi: 10.1038/sj.bjp.0702912.
7
Electrospray mass spectrometric analysis of 5-hydroperoxy and 5-hydroxyeicosatetraenoic acids generated by lipid peroxidation of red blood cell ghost phospholipids.红细胞膜空壳磷脂脂质过氧化生成的5-氢过氧二十碳四烯酸和5-羟基二十碳四烯酸的电喷雾质谱分析
J Am Soc Mass Spectrom. 1998 May;9(5):527-32. doi: 10.1016/S1044-0305(98)00013-0.
8
Pharmacological inhibition of leukotriene actions.白三烯作用的药理学抑制
Pharm World Sci. 1998 Apr;20(2):60-5. doi: 10.1023/a:1008698027211.
9
Leukotriene B4 and asthma.白三烯B4与哮喘
Thorax. 1996 Dec;51(12):1171-3. doi: 10.1136/thx.51.12.1171.
10
Clinical management of asthma in the 1990s. Current therapy and new directions.20世纪90年代哮喘的临床管理。当前的治疗方法与新方向。
Drugs. 1996;52 Suppl 6:1-11. doi: 10.2165/00003495-199600526-00003.

本文引用的文献

1
The human PMN leukocyte chemotactic activity of complex hydroxy-eicosatetraenoic acids (HETEs).复合羟基二十碳四烯酸(HETEs)的人中性粒细胞趋化活性。
J Immunol. 1980 Oct;125(4):1789-91.
2
Preparation and characterization of hydroperoxy-eicosatetraenoic acids (HPETEs).氢过氧化二十碳四烯酸(HPETEs)的制备与表征
Prostaglandins. 1980 Jan;19(1):87-97. doi: 10.1016/0090-6980(80)90156-2.
3
Enhanced expression of human monocyte complement (C3b) receptors by chemoattractants.趋化因子对人单核细胞补体(C3b)受体表达的增强作用。
Clin Exp Immunol. 1980 Mar;39(3):768-75.
4
Lipoxygenbase-derived products of arachidonic acid mediate stimulation of hexose uptake in human polymorphonuclear leukocytes.花生四烯酸的脂氧合酶衍生产物介导人多形核白细胞中己糖摄取的刺激。
Biochem Biophys Res Commun. 1981 May 15;100(1):1-7. doi: 10.1016/s0006-291x(81)80054-x.
5
Novel structural determinants of the human neutrophil chemotactic activity of leukotriene B.白三烯B对人中性粒细胞趋化活性的新型结构决定因素
J Exp Med. 1981 Feb 1;153(2):482-7. doi: 10.1084/jem.153.2.482.
6
Mono- and dihydroxyeicosatetraenoic acids alter calcium homeostasis in rabbit neutrophils.单羟基和二羟基二十碳四烯酸改变兔中性粒细胞的钙稳态。
J Clin Invest. 1981 May;67(5):1584-7. doi: 10.1172/jci110191.
7
Leukotriene B, a potent chemokinetic and aggregating substance released from polymorphonuclear leukocytes.白三烯B,一种从多形核白细胞释放的强效化学趋化和聚集物质。
Nature. 1980 Jul 17;286(5770):264-5. doi: 10.1038/286264a0.
8
Slow reacting substances of anaphylaxis: identification of leukotrienes C-1 and D from human and rat sources.过敏反应迟缓反应物质:从人和大鼠来源中鉴定白三烯C-1和D
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3710-4. doi: 10.1073/pnas.77.6.3710.
9
Leukotriene D: a slow reacting substance from rat basophilic leukemia cells.白三烯D:一种来自大鼠嗜碱性白血病细胞的慢反应物质。
Proc Natl Acad Sci U S A. 1980 Apr;77(4):2014-7. doi: 10.1073/pnas.77.4.2014.
10
Studies on eosinophil leucocyte migration. II. Factors specifically chemotactic for eosinophils and neutrophils generated from guinea-pig serum by antigen-antibody complexes.嗜酸性白细胞迁移的研究。II. 抗原抗体复合物从豚鼠血清中产生的对嗜酸性粒细胞和中性粒细胞具有特异性趋化作用的因子。
Clin Exp Immunol. 1970 Nov;7(5):723-37.

白三烯及其他脂氧合酶产物对人中性粒细胞和嗜酸性粒细胞补体受体的增强作用及趋化作用。

Complement receptor enhancement and chemotaxis of human neutrophils and eosinophils by leukotrienes and other lipoxygenase products.

作者信息

Nagy L, Lee T H, Goetzl E J, Pickett W C, Kay A B

出版信息

Clin Exp Immunol. 1982 Mar;47(3):541-7.

PMID:6282507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1536414/
Abstract

The lipoxygenase products of arachidonic acid, 5-HPETE, 5-HETE, LTB4, LTC4 and LTD4, were examined for their capacity to enhance the expression of complement (C3b) receptors and to evoke chemotaxis of human neutrophils and eosinophils. With the exception of LTD4 all gave enhancement of C3b receptors. LTB4 and LTC4 enhanced over the concentration range 10(-7) to 10(-11) moles/l, and 5-HETE and 5-HPETE from 5 X 10(-6) to 5 X 10(-10) moles/l. The rank order of activity, as assessed by the magnitude of enhancement, was LTB4 (concentration for maximal effect = 10(-7) moles/l) greater than 5-HETE (5 X 10(-7)) greater than 5-HPETE (5 X 10(-6)) greater than LTC4 (10(-9)). High dose inhibition was observed with LTC4 and 5-HETE. Chemotaxis experiments performed in parallel over the same concentration ranges indicated that neither neutrophils nor eosinophils migrated towards LTC4 or LTD4. However, LTB4 evoked chemotaxis with a linear dose response from 10(-9) to 10(-7) moles/l and 5-HPETE and 5-HETE from 5 X 10(-8) to 5 X 10(-6) moles/l. At 10(-7) moles/l LTB4 was approximately 6 and 8 X more potent in chemotaxis than 5-HPETE and 5-HETE respectively. In general, complement receptor enhancement and chemotaxis of eosinophils were similar to that observed with neutrophils and did not vary with the patient source.

摘要

对花生四烯酸的脂氧合酶产物5 - HPETE、5 - HETE、LTB4、LTC4和LTD4进行了检测,以考察它们增强补体(C3b)受体表达以及引起人中性粒细胞和嗜酸性粒细胞趋化性的能力。除LTD4外,其他产物均能增强C3b受体表达。LTB4和LTC4在10^(-7)至10^(-11)摩尔/升的浓度范围内增强受体表达,5 - HETE和5 - HPETE在5×10^(-6)至5×10^(-10)摩尔/升的浓度范围内增强受体表达。根据增强程度评估的活性顺序为:LTB4(最大效应浓度 = 10^(-7)摩尔/升)>5 - HETE(5×10^(-7))>5 - HPETE(5×10^(-6))>LTC4(10^(-9))。观察到LTC4和5 - HETE存在高剂量抑制作用。在相同浓度范围内并行进行的趋化性实验表明,中性粒细胞和嗜酸性粒细胞均未向LTC4或LTD4迁移。然而,LTB4在10^(-9)至10^(-7)摩尔/升的浓度范围内引起趋化性,呈线性剂量反应,5 - HPETE和5 - HETE在5×10^(-8)至5×10^(-6)摩尔/升的浓度范围内引起趋化性。在10^(-7)摩尔/升时,LTB4在趋化性方面的效力分别比5 - HPETE和5 - HETE强约6倍和8倍。一般来说,嗜酸性粒细胞的补体受体增强和趋化性与中性粒细胞相似,且不随患者来源而变化。