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选择素——炎症治疗干预的糖蛋白靶点。

Selectins--glycoprotein targets for therapeutic intervention in inflammation.

作者信息

Parekh R B, Edge C J

机构信息

Oxford GlycoSystems, Blacklands Way, Abingdon, UK.

出版信息

Trends Biotechnol. 1994 Sep;12(9):339-45. doi: 10.1016/0167-7799(94)90034-5.

DOI:10.1016/0167-7799(94)90034-5
PMID:7521172
Abstract

Inflammation can be a beneficial response in the host for the control of infection and injury. However, occasionally, the inflammatory response can result in acute systemic collapse or, more frequently, a chronic reaction such as that observed in autoimmune disease, Crohn's disease and asthma. Injury to tissues or organs results in leukocyte adhesion to the endothelial cell surface, followed by diapedesis. Investigation of the initial leukocyte-endothelium adhesion processes has clearly shown the involvement of an inducible set of molecules, called selectins, on the endothelial and leukocyte cell surfaces. These molecules are of interest as the interactions with their respective ligands appear to involve carbohydrates. The exact nature of these interactions is still being elucidated. Therapeutic intervention using carbohydrate small-molecule mimetics may be beneficial in the modification of the inflammatory process.

摘要

炎症在宿主体内可能是一种控制感染和损伤的有益反应。然而,炎症反应偶尔会导致急性全身性衰竭,或者更常见的是引发慢性反应,如在自身免疫性疾病、克罗恩病和哮喘中观察到的那样。组织或器官损伤会导致白细胞黏附于内皮细胞表面,随后发生白细胞渗出。对白细胞与内皮细胞初始黏附过程的研究清楚地表明,在内皮细胞和白细胞表面存在一组可诱导的分子,称为选择素。这些分子备受关注,因为它们与各自配体的相互作用似乎涉及碳水化合物。这些相互作用的确切性质仍在阐明之中。使用碳水化合物小分子模拟物进行治疗干预可能有助于改变炎症过程。

相似文献

1
Selectins--glycoprotein targets for therapeutic intervention in inflammation.选择素——炎症治疗干预的糖蛋白靶点。
Trends Biotechnol. 1994 Sep;12(9):339-45. doi: 10.1016/0167-7799(94)90034-5.
2
The selectin family of carbohydrate-binding proteins: structure and importance of carbohydrate ligands for cell adhesion.碳水化合物结合蛋白的选择素家族:碳水化合物配体对细胞黏附的结构及重要性
Bioessays. 1992 Dec;14(12):849-56. doi: 10.1002/bies.950141210.
3
B lymphocyte binding to E- and P-selectins is mediated through the de novo expression of carbohydrates on in vitro and in vivo activated human B cells.B淋巴细胞与E-选择素和P-选择素的结合是通过体外和体内活化的人B细胞上碳水化合物的从头表达介导的。
J Clin Invest. 1994 Oct;94(4):1585-96. doi: 10.1172/JCI117500.
4
The selectins: vascular adhesion molecules.选择素:血管黏附分子
FASEB J. 1995 Jul;9(10):866-73.
5
Leukocyte adhesion molecule-1 (LAM-1, L-selectin) interacts with an inducible endothelial cell ligand to support leukocyte adhesion.白细胞黏附分子-1(LAM-1,L-选择素)与一种可诱导的内皮细胞配体相互作用以支持白细胞黏附。
J Immunol. 1991 Oct 15;147(8):2565-73.
6
The selectins and their ligands.选择素及其配体。
Curr Opin Cell Biol. 1994 Oct;6(5):663-73. doi: 10.1016/0955-0674(94)90092-2.
7
Cell surface lectins in the immune system.免疫系统中的细胞表面凝集素。
Semin Immunol. 1993 Aug;5(4):237-47. doi: 10.1006/smim.1993.1028.
8
Leukocyte interactions with vascular endothelium. New insights into selectin-mediated attachment and rolling.白细胞与血管内皮的相互作用。对选择素介导的黏附和滚动的新见解。
J Immunol. 1995 Jul 15;155(2):525-8.
9
Selectin ligands.选择素配体
Proc Natl Acad Sci U S A. 1994 Aug 2;91(16):7390-7. doi: 10.1073/pnas.91.16.7390.
10
Kinetic expression of endothelial adhesion molecules and relationship to leukocyte recruitment in two cutaneous models of inflammation.两种皮肤炎症模型中内皮黏附分子的动力学表达及其与白细胞募集的关系。
Lab Invest. 1994 Feb;70(2):163-75.

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剪切力调节人内皮细胞中 IL-1β 诱导的 E-选择素表达。
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Solution structure of a Lewis(x) analogue by off-resonance 1H NMR spectroscopy without use of an internal distance reference.
J Biomol NMR. 1996 Jul;8(1):23-35. doi: 10.1007/BF00198137.
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[Protein-carbohydrate recognition. Foundation and medical application with illustrations of tumor lectin studies].[蛋白质-碳水化合物识别。基础与医学应用,附肿瘤凝集素研究实例]
Naturwissenschaften. 1995 Dec;82(12):533-43.
6
A model for the initial phase of cell/surface interactions based on ligand binding phenomena.基于配体结合现象的细胞/表面相互作用初始阶段模型。
Biochem J. 1995 Nov 1;311 ( Pt 3)(Pt 3):917-9. doi: 10.1042/bj3110917.