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实验性炎症性肠病中的白细胞迁移。

Leukocyte migration in experimental inflammatory bowel disease.

机构信息

Department of Cell Biology and Immunology Faculty of Medicine Vrije Universiteit Van der Boechorststraat 7 Amsterdam 1081 BT The Netherlands.

出版信息

Mediators Inflamm. 1997;6(2):85-93. doi: 10.1080/09629359791776.

DOI:10.1080/09629359791776
PMID:18472841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2365857/
Abstract

Emigration of leukocytes from the circulation into tissue by transendothelial migration, is mediated subsequently by adhesion molecules such as selectins, chemokines and integrins. This multistep paradigm, with multiple molecular choices at each step, provides a diversity in signals. The influx of neutrophils, monocytes and lymphocytes into inflamed tissue is important in the pathogenesis of chronic inflammatory bowel disease. The importance of each of these groups of adhesion molecules in chronic inflammatory bowel disease, either in human disease or in animal models, will be discussed below. Furthermore, the possibilities of blocking these different steps in the process of leukocyte extravasation in an attempt to prevent further tissue damage, will be taken into account.

摘要

白细胞从血液循环中穿过血管内皮迁移到组织中,随后通过黏附分子(如选择素、趋化因子和整合素)介导。这种多步骤范例在每个步骤都有多个分子选择,提供了多样性的信号。中性粒细胞、单核细胞和淋巴细胞流入炎症组织在慢性炎症性肠病的发病机制中很重要。下面将讨论这些黏附分子在慢性炎症性肠病中的重要性,无论是在人类疾病还是动物模型中。此外,还将考虑阻断白细胞渗出过程中的这些不同步骤的可能性,以防止进一步的组织损伤。

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引用本文的文献

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Transmigrating neutrophils shape the mucosal microenvironment through localized oxygen depletion to influence resolution of inflammation.迁移中性粒细胞通过局部耗氧来塑造黏膜微环境,从而影响炎症的消退。
Immunity. 2014 Jan 16;40(1):66-77. doi: 10.1016/j.immuni.2013.11.020. Epub 2014 Jan 9.
2
The puzzling inflammatory bowel disease: growing interest for mediators of inflammation.令人困惑的炎症性肠病:对炎症介质的兴趣与日俱增。
Mediators Inflamm. 1997;6(2):83-4. doi: 10.1080/09629359791767.

本文引用的文献

1
Intestinal inflammation in TNBS sensitized rats as a model of chronic inflammatory bowel disease.TNBS 敏化大鼠的肠道炎症作为慢性炎症性肠病模型。
Mediators Inflamm. 1992;1(2):121-6. doi: 10.1155/S0962935192000206.
2
Structure/activity studies of anti-inflammatory peptides based on a conserved peptide region of the lectin domain of E-, L- and P-selectin.基于E-、L-和P-选择素凝集素结构域保守肽区域的抗炎肽的结构/活性研究
Glycobiology. 1996 Dec;6(8):831-6. doi: 10.1093/glycob/6.8.831.
3
Enhanced expression and production of monocyte chemoattractant protein-1 in inflammatory bowel disease mucosa.炎症性肠病黏膜中单核细胞趋化蛋白-1的表达及产生增强。
J Leukoc Biol. 1996 Jun;59(6):804-12. doi: 10.1002/jlb.59.6.804.
4
Differential in situ expression of the genes encoding the chemokines MCP-1 and RANTES in human inflammatory bowel disease.趋化因子MCP-1和RANTES编码基因在人类炎症性肠病中的差异原位表达
J Pathol. 1996 Feb;178(2):201-6. doi: 10.1002/(SICI)1096-9896(199602)178:2<201::AID-PATH440>3.0.CO;2-4.
5
Circulating soluble adhesion molecules in inflammatory bowel disease.炎症性肠病中的循环可溶性黏附分子
Eur J Gastroenterol Hepatol. 1995 Nov;7(11):1037-41. doi: 10.1097/00042737-199511000-00005.
6
Analysis of bovine gamma delta T cell interactions with E-, P-, and L-selectin. Characterization of lymphocyte on lymphocyte rolling and the effects of O-glycoprotease.牛γδ T细胞与E-、P-和L-选择素相互作用的分析。淋巴细胞间滚动的特征及O-糖蛋白酶的作用。
J Immunol. 1996 Jan 1;156(1):289-96.
7
Interleukin 8: cells of origin in inflammatory bowel disease.白细胞介素8:炎症性肠病中的细胞起源
Gut. 1996 Jan;38(1):90-8. doi: 10.1136/gut.38.1.90.
8
Peptides inhibit selectin-mediated cell adhesion in vitro, and neutrophil influx into inflammatory sites in vivo.肽类在体外可抑制选择素介导的细胞黏附,并在体内抑制中性粒细胞流入炎症部位。
Glycobiology. 1995 Sep;5(6):583-8. doi: 10.1093/glycob/5.6.583.
9
Cytokines in intestinal inflammation: pathophysiological and clinical considerations.肠道炎症中的细胞因子:病理生理学及临床考量
Gastroenterology. 1994 Feb;106(2):533-9. doi: 10.1016/0016-5085(94)90614-9.
10
Serum interleukin-8 in inflammatory bowel disease.炎症性肠病中的血清白细胞介素-8
J Gastroenterol Hepatol. 1993 Nov-Dec;8(6):508-12. doi: 10.1111/j.1440-1746.1993.tb01643.x.