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硫酸乙酰肝素蛋白聚糖参与阿片受体介导的细胞迁移。

Heparan sulfate proteoglycans are involved in opiate receptor-mediated cell migration.

作者信息

Kaneider Nicole C, Dunzendorfer Stefan, Wiedermann Christian J

机构信息

Division of General Internal Medicine, Department of Internal Medicine, University of Innsbruck, Anichstrasse 35, A-6020 Innsbruck, Austria.

出版信息

Biochemistry. 2004 Jan 13;43(1):237-44. doi: 10.1021/bi035295i.

Abstract

Opioid receptors are expressed in cells of the immune system, and potent immunomodulatory effects of their natural and synthetic ligands have been reported. In some studies, the opiate receptor antagonist naloxone itself displayed immunomodulatory actions. We investigated effects of naloxone on leukocyte chemotaxis. Cell migration was tested in micropore filter assays using modified Boyden chambers, and receptor expression was investigated using radiolabel binding assays. Naloxone induced peripheral blood nonadherent mononuclear cell and neutrophil chemotaxis at nanomolar concentrations and deactivated their migration toward beta-endorphin, angiotensin II, somatostatin, or interleukin-8 but not toward RANTES, vasoactive intestinal peptide, or substance P. Ligand binding studies showed no alteration in the binding of interleukin-8 to neutrophils by naloxone. Cleavage of heparan sulfate from proteoglycans on the cells' surface completely inhibited chemotactic and deactivating properties of naloxone but not other attractants. Chemotactic properties were abolished by pretreating cells with heparinase, chondroitinase, sodium chlorate, and anti-syndecan-4 antibodies, indicating the involvement of syndecan-4. The extent of migration toward naloxone was diminished by pretreatment with dimethylsphingosine, a specific sphingosine kinase inhibitor. As syndecan-4 signaling in leukocyte chemotaxis involves activation of sphingosine kinase, results indicate that naloxone interacts with syndecan-4 function in cell migration and suggest a role for heparan sulfate proteoglycans as coreceptors to members of the delta-opiate receptor family.

摘要

阿片受体在免疫系统细胞中表达,并且其天然和合成配体具有强大的免疫调节作用已见报道。在一些研究中,阿片受体拮抗剂纳洛酮自身就表现出免疫调节作用。我们研究了纳洛酮对白细胞趋化性的影响。在使用改良博伊登小室的微孔滤膜分析中测试细胞迁移,并使用放射性标记结合分析研究受体表达。纳洛酮在纳摩尔浓度时可诱导外周血非黏附单核细胞和中性粒细胞趋化,并使它们向β-内啡肽、血管紧张素II、生长抑素或白细胞介素-8的迁移失活,但不影响向调节激活正常T细胞表达和分泌因子(RANTES)、血管活性肠肽或P物质的迁移。配体结合研究表明纳洛酮对白细胞介素-8与中性粒细胞的结合无改变。从细胞表面蛋白聚糖上切割硫酸乙酰肝素完全抑制了纳洛酮的趋化和失活特性,但对其他趋化剂无影响。用肝素酶、软骨素酶、氯酸钠和抗syndecan-4抗体预处理细胞可消除趋化特性,表明syndecan-4参与其中。用特异性鞘氨醇激酶抑制剂二甲基鞘氨醇预处理可减少向纳洛酮的迁移程度。由于syndecan-4在白细胞趋化中的信号传导涉及鞘氨醇激酶的激活,结果表明纳洛酮在细胞迁移中与syndecan-4功能相互作用,并提示硫酸乙酰肝素蛋白聚糖作为δ-阿片受体家族成员的共受体发挥作用。

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