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选择素:血管黏附分子

The selectins: vascular adhesion molecules.

作者信息

Tedder T F, Steeber D A, Chen A, Engel P

机构信息

Department of Immunology, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

FASEB J. 1995 Jul;9(10):866-73.

PMID:7542213
Abstract

The selectin family of adhesion molecules mediates the initial attachment of leukocytes to venular endothelial cells before their firm adhesion and diapedesis at sites of tissue injury and inflammation. The selectin family consists of three closely related cell-surface molecules with differential expression by leukocytes (L-selectin), platelets (P-selectin), and vascular endothelium (E- and P-selectin). The selectins have characteristic extracellular regions composed of an amino-terminal lectin domain that binds a carbohydrate ligand, an epidermal growth factor-like domain, and two to nine short repeat units homologous to domains found in complement binding proteins. In contrast to most other adhesion molecules, selectin function is restricted to leukocyte interactions with vascular endothelium. Multiple studies indicate that the selectins mediate neutrophil, monocyte, and lymphocyte rolling along the venular wall. The generation of selectin-deficient mice has confirmed these findings and provided further insight into how the overlapping functions of these receptors regulate inflammatory processes. Selectin-directed therapeutic agents are now proven to be effective in blocking many of the pathological effects resulting from leukocyte entry into sites of inflammation. Future studies are focused on how the selectins interact with the increasing array of other adhesion molecules and inflammatory mediators.

摘要

黏附分子选择素家族介导白细胞在组织损伤和炎症部位牢固黏附及穿出血管之前,与小静脉内皮细胞的初始黏附。选择素家族由三个密切相关的细胞表面分子组成,白细胞(L-选择素)、血小板(P-选择素)和血管内皮(E-选择素和P-选择素)对其有不同表达。选择素具有特征性的细胞外区域,由一个结合碳水化合物配体的氨基末端凝集素结构域、一个表皮生长因子样结构域以及两到九个与补体结合蛋白中发现的结构域同源的短重复单元组成。与大多数其他黏附分子不同,选择素的功能仅限于白细胞与血管内皮的相互作用。多项研究表明,选择素介导中性粒细胞、单核细胞和淋巴细胞沿小静脉壁滚动。选择素缺陷小鼠的产生证实了这些发现,并进一步深入了解了这些受体的重叠功能如何调节炎症过程。现已证明,针对选择素的治疗药物可有效阻断白细胞进入炎症部位所产生的许多病理效应。未来的研究集中于选择素如何与越来越多的其他黏附分子和炎症介质相互作用。

相似文献

1
The selectins: vascular adhesion molecules.选择素:血管黏附分子
FASEB J. 1995 Jul;9(10):866-73.
2
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.
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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.
4
P-selectin mediates the interaction of circulating leukocytes with platelets and microvascular endothelium in response to oxidized lipoprotein in vivo.在体内,P选择素介导循环白细胞与血小板及微血管内皮细胞之间的相互作用,以应对氧化脂蛋白。
Lab Invest. 1994 Sep;71(3):380-6.
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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.
6
Lectin cell adhesion molecules (LEC-CAMs): a new family of cell adhesion proteins involved with inflammation.凝集素细胞黏附分子(LEC-CAMs):参与炎症反应的一类新的细胞黏附蛋白家族。
J Cell Biochem. 1991 Feb;45(2):139-46. doi: 10.1002/jcb.240450204.
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
L-selectin binds to P-selectin glycoprotein ligand-1 on leukocytes: interactions between the lectin, epidermal growth factor, and consensus repeat domains of the selectins determine ligand binding specificity.L-选择素与白细胞上的P-选择素糖蛋白配体-1结合:选择素的凝集素、表皮生长因子和共有重复结构域之间的相互作用决定了配体结合特异性。
J Immunol. 1996 Nov 1;157(9):3995-4004.
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In vivo and in vitro functional examination of a conserved epitope of L- and E-selectin crucial for leukocyte-endothelial cell interactions.对L-选择素和E-选择素保守表位进行体内和体外功能检测,该表位对白细胞与内皮细胞相互作用至关重要。
J Immunol. 1994 Jun 15;152(12):5814-25.
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GMP-140: a receptor for neutrophils and monocytes on activated platelets and endothelium.GMP - 140:活化血小板和内皮细胞上的中性粒细胞及单核细胞受体。
J Cell Biochem. 1991 Feb;45(2):156-61. doi: 10.1002/jcb.240450206.

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